Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review
Open accessAbstract
Post-exercise recovery strategies influence the body’s ability to restore physiological homeostasis, replenish energy stores, repair muscle damage, and promote desired adaptations, which improve exercise performance. This narrative review examines the impact of nutritional strategies commonly used for enhancing recovery and subsequent exercise performance, particularly when athletes face short recovery periods. Carbohydrate ingestion is essential for glycogen replenishment, especially within the initial hours post-exercise, with its impact dependent on the types, timing, and amount. Protein is essential for accelerating muscle recovery and achieving a positive nitrogen balance, depending on the type and dosage. The co-ingestion of carbohydrates with proteins or fats is explored for its role in maximizing glycogen resynthesis and muscle repair, with evidence supporting the addition of protein to suboptimal carbohydrate intake for enhanced recovery. Moreover, this review addresses the potential benefits of creatine and caffeine co-ingestion for accelerating glycogen synthesis and improving subsequent performance. Hydration strategies, including the use of milk-based beverages and electrolyte solutions, are also discussed, emphasizing their importance in maintaining fluid balance and optimizing recovery. This review also highlights the emerging role of micronutrients such as omega-3 fatty acids, antioxidants, and sodium bicarbonate in reducing muscle damage and improving acid–base balance. Evidence supports the tailored use of these nutritional strategies, particularly for athletes managing tight competition/training schedules. Future research should focus on refining individualized approaches for recovery and investigating the impact of novel supplements on subsequent performance.
AI snapshot
Written from the paper’s full text.
TL;DR
This narrative review synthesizes nutritional strategies for post-exercise recovery and subsequent exercise performance, defined as performance within ~2–24 h after a prior exhaustive bout. Carbohydrate and protein are central, with conditional evidence for creatine, caffeine, sodium bicarbonate, hydration, fats, and micronutrients.
Key findings
- Carbohydrate ingestion of 1–1.2 g·kg⁻¹·h⁻¹ during the initial 4 h post-exercise is recommended, with glucose/glucose-derived sources and optional fructose co-ingestion; glucose–fructose improved subsequent endurance capacity by ~33% and ~27% in two studies versus glucose alone, but other performance studies found no benefit. Complete muscle glycogen replenishment typically takes 24–36 h with 7–12 g·kg⁻¹ carbohydrate per day; high-GI carbohydrate increased 24-h glycogen (~106 vs 72 mmol·kg⁻¹ wet weight) but performance effects were inconsistent.
- Protein at 20–40 g post-exercise maximizes muscle protein synthesis for 3–4 h; endurance athletes are advised ~1.2–1.8 g·kg⁻¹·day⁻¹ and power athletes 1.7–2.2 g·kg⁻¹·day⁻¹. Carbohydrate–protein co-ingestion has small positive performance effects (~0.6–1.6%), with examples of ~14 min and ~8.5 min longer subsequent exercise capacity, especially when added to suboptimal carbohydrate.
- Creatine plus carbohydrate may enhance glycogen storage (e.g., 82% greater resynthesis within 24 h; 18% increase after 5 days of 20 g·day⁻¹ loading; 53% with moderate carbohydrate), but effects on subsequent performance remain debated. Caffeine–carbohydrate co-ingestion shows mixed glycogen and performance results; sodium bicarbonate after exercise may restore acid–base balance and improve subsequent performance with 30–90 min recovery, though 35 min may be inadequate.
- Rehydration should replace 125–150% of body mass lost; milk-based beverages, oral rehydration solutions, and water with solid meals can support recovery, while water alone has low beverage hydration index. Dietary fats have limited evidence and no clear effect on subsequent performance; micronutrients reduce exercise-induced muscle damage but not consistently performance, with >1000 mg polyphenols/day for at least 3 days recommended.
Methods
- Narrative review with literature searched in PubMed/MEDLINE and Google Scholar using keyword and Boolean combinations covering carbohydrate, protein, fat, creatine, sodium bicarbonate, caffeine, micronutrients, and fluids/electrolytes.
- Evidence was classified as grade I (strong), grade II (moderate), or grade III (limited) based on consistency and volume of controlled trials.
- The review synthesized findings on recovery and subsequent exercise performance occurring within ~2–24 h of prior exhaustive exercise; no systematic meta-analysis or formal risk-of-bias assessment is reported.
Limitations
- Stated by the authors: much of the literature is based on male athletes, creating potential sex bias; exercise protocols vary and may not reflect real-world conditions; responses to creatine and caffeine co-ingestion are highly individualized; personalization literature is lacking; supplement interactions may not be additive; more research is needed in real-world sports, team sports, ultra-endurance events, and resistance-training athletes training twice daily.
- Evident from the text: as a narrative review, it does not systematically quantify study quality or pool effect sizes; many cited studies use different doses, timing, glycogen-depletion protocols, and performance tests, and several conclusions rely on markers of muscle damage or glycogen rather than subsequent performance.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
43 of 83 cited sources checked · 10 supported · 1 flagged · accuracy not yet measured
- Interpretationcitation
There is currently no evidence to recommend consuming more than 1.2 g·kg−1⋅h−1 of carbohydrates, regardless of type.
“There is currently no evidence to recommend consuming more than 1.2 g·kg−1⋅h−1 of carbohydrates, regardless of type [22, 25].”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [22] Trommelen J, et al. Fructose coingestion does not accelerate postexercise muscle glycogen repletion. Med Sci Sports Exerc. 2016;48(5):907–12. source
- cites [25] Fuchs CJ, et al. Sucrose ingestion after exhaustive exercise accelerates liver, but not muscle glycogen repletion compared with glucose ingestion in trained athletes. J Appl Physiol. 2016;120(11):1328–34. source
The NEW & NOTEWORTHY passage explicitly recommends sucrose at 1.5 g·kg−1·h−1 over glucose when rapid recovery of endogenous carbohydrate stores is the goal. Although the DISCUSSION says 1.2 g·kg−1·h−1 maximizes postexercise muscle glycogen synthesis, the paper reports faster liver glycogen repletion with sucrose at 1.5 g·kg−1·h−1. The claim's blanket statement, regardless of carbohydrate type, conflicts with that recommendation. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
- Premisecitation
Replenishing glycogen stores through immediate post-exercise carbohydrate intake is crucial for recovery, especially when athletes need to be fully prepared for another training session or competition within 24 h.
“Replenishing glycogen stores through immediate post-exercise carbohydrate intake is crucial for recovery, especially when athletes need to be fully prepared for another training session or competition within 24 h [7–9].”
Quote in the paperSubstantial claim2 of 3 sources checked- cites [7] Bonilla DA, et al. The 4R’s framework of nutritional strategies for post-exercise recovery: a review with emphasis on new generation of carbohydrates. Int J Environ Res Public Health. 2021;18(1):103. source
- cites [8] Fuchs CJ, Gonzalez JT, van Loon LJC. Fructose co-ingestion to increase carbohydrate availability in athletes. J Physiol. 2019;597(14):3549–60. source
- cites [9] Ivy JL. Regulation of muscle glycogen repletion, muscle protein synthesis and repair following exercise. J Sports Sci Med. 2004;3(3):131–8.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Complete replenishment of muscle glycogen stores typically unfolds over a 24-36 h period post-exercise, provided that 7-12 g·kg−1 carbohydrate are consumed per day.
“Complete replenishment of muscle glycogen stores typically unfolds over a 24–36 h period post-exercise, provided that 7–12 g·kg−1 carbohydrate are consumed per day [15–18].”
Quote in the paperSubstantial claim4 of 4 sources checked- cites [15] Burke LM, et al. Carbohydrates for training and competition. J Sports Sci. 2011;29(Suppl 1):S17-27. source
In “Acute strategies to promote high carbohydrate availability for exercise” (page unavailable), the paper says glycogen stores can normalize within 24 hours with reduced training and adequate fuel, and that high glycogen concentrations can be achieved with 24–36 hours of high carbohydrate intake and rest. Table II gives 7–12 g/kg per 24 hours for general fuelling, but does not establish that this entire intake range typically produces complete post-exercise replenishment in 24–36 hours. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [16] Gonzalez JT, Betts JA. Dietary sugars, exercise and hepatic carbohydrate metabolism. Proc Nutr Soc. 2019;78(2):246–56. source
The Exercise performance section says muscle glycogen may take 20–24 h to fully recover after exhaustive exercise with high carbohydrate intake, or up to 46 h on a moderate-carbohydrate diet (page unavailable in our copy). It does not give the claimed 24–36 h range or specify 7–12 g/kg of carbohydrate per day; its intake recommendation is 1–1.2 g/kg per hour during the first 4 h of recovery. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [17] Murray B, Rosenbloom C. Fundamentals of glycogen metabolism for coaches and athletes. Nutr Rev. 2018;76(4):243–59. source
The Time Course of Glycogen Replenishment section says adequate carbohydrate can restore muscle glycogen within 24 hours, and Other Nutrient Interventions specifies at least 24 hours of rest with 10 g/kg/day for full restoration. The paper does not give 24–36 hours as the typical period or 7–12 g/kg/day as the requisite intake; Glycogen Resynthesis After Exercise also says sufficient total energy is needed. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [18] Podlogar T, Wallis GA. New horizons in carbohydrate research and application for endurance athletes. Sports Med. 2022;52(Suppl 1):5–23. source
The Post-Competition section says full muscle-glycogen repletion is believed to require 24–36 hours. It recommends an initial hourly carbohydrate intake when rapid repletion is needed, followed by a diet that may provide up to 12 g/kg daily; it does not give a 7–12 g/kg daily range or say that this range ensures complete repletion. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Premisecitation
Delaying post-exercise carbohydrate ingestion by 2 h may impair exercise performance the following day.
“and may impair exercise performance the following day [14]”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [14] Díaz-Lara J, et al. Delaying post-exercise carbohydrate intake impairs next-day exercise capacity but not muscle glycogen or molecular responses. Acta Physiol (Oxf). 2024;240(10): e14215. source
The Discussion reports reduced next-day high-intensity exercise capacity after delaying post-exercise carbohydrate intake. It specifies a 3-hour delay, not the 2-hour delay in the attributed claim; no page number is available in our copy. (LLM, conf=0.90)
Experimental — accuracy not yet measured
- Premisecitation
Liver glycogen resynthesis proceeds at a slower pace during the initial post-exercise hours, achieving saturation only after 11-25 h, contingent upon adherence to a high-carbohydrate diet.
“Liver glycogen resynthesis proceeds at a slower pace during the initial post-exercise hours, achieving saturation only after 11–25 h, contingent upon adherence to a high-carbohydrate diet [16].”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [16] Gonzalez JT, Betts JA. Dietary sugars, exercise and hepatic carbohydrate metabolism. Proc Nutr Soc. 2019;78(2):246–56. source
The Exercise performance section reports that liver glycogen resynthesis is about 30–50% slower in the first 2 hours than at 3–5 hours post-exercise. It estimates 11 hours with glucose–fructose mixtures and about 25 hours with glucose alone, but those times are extrapolations under high carbohydrate ingestion, not observed saturation times or a general requirement for a high-carbohydrate diet. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
The total amount of protein plays a more important role than the timing of protein-rich meals.
“However, it seems that more than the timing of the meals, the total amount of protein plays a more important role than the timing itself [53, 68].”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [53] Pasiakos SM, Lieberman HR, McLellan TM. Effects of protein supplements on muscle damage, soreness and recovery of muscle function and physical performance: a systematic review. Sports Med. 2014;44(5):655–70. source
- cites [68] Trommelen J, et al. The anabolic response to protein ingestion during recovery from exercise has no upper limit in magnitude and duration in vivo in humans. Cell Rep Med. 2023;4(12): 101324. source
The Discussion reports that a single large protein dose produces prolonged anabolism, allowing more flexibility in meal timing. However, the study compared single doses after exercise; it did not directly compare total daily protein intake with meal timing or establish which is more important. (LLM, conf=0.82)
Experimental — accuracy not yet measured
- Interpretationcitation
The influence of glycemic index on subsequent exercise performance appears inconsistent.
“However, the influence of GI on subsequent exercise performance appears inconsistent.”
Quote in the paperSubstantial claim1 of 5 sources checked- cites [39] Wong SH, et al. Effect of glycemic index meals on recovery and subsequent endurance capacity. Int J Sports Med. 2009;30(12):898–905. source
- cites [40] Erith S, et al. The effect of high carbohydrate meals with different glycemic indices on recovery of performance during prolonged intermittent high-intensity shuttle running. Int J Sport Nutr Exerc Metab. 2006;16(4):393–404. source
- cites [41] Stevenson E, et al. Influence of the glycaemic index of an evening meal on substrate oxidation following breakfast and during exercise the next day in healthy women. Eur J Clin Nutr. 2008;62(5):608–16. source
- cites [42] Brown LJ, et al. High versus low glycemic index 3-h recovery diets following glycogen-depleting exercise has no effect on subsequent 5-km cycling time trial performance. J Sci Med Sport. 2013;16(5):450–4. source
- cites [43] Stevenson E, Williams C, Nute M. The influence of the glycaemic index of breakfast and lunch on substrate utilisation during the postprandial periods and subsequent exercise. Br J Nutr. 2005;93(6):885–93. source
The study’s Abstract and Discussion report substrate utilisation during a fixed-duration run, not whether GI affects exercise performance inconsistently. A search for exercise performance and conflicting findings found references to performance studies, but no passage in our copy assessing the consistency of their results. (LLM, conf=0.76)
Experimental — accuracy not yet measured
- Premisecitation
The benefit of protein added to carbohydrate appears to occur only when protein is added to a suboptimal amount of carbohydrate (e.g., 0.3 g·kg−1·h−1 protein and 0.9 g·kg−1⋅h−1 carbohydrate).
“However, this benefit appears to occur only when protein is added to a suboptimal amount of carbohydrate (e.g., 0.3 g·kg⁻1·h⁻1 protein and 0.9 g·kg−1⋅h−1 carbohydrate) [85].”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [85] Margolis LM, et al. Coingestion of carbohydrate and protein on muscle glycogen synthesis after exercise: a meta-analysis. Med Sci Sports Exerc. 2021;53(2):384–93. source
The Conclusion proposes 0.9 g·kg−1·h−1 carbohydrate plus 0.3 g·kg−1·h−1 protein as a way to support overall postexercise recovery. But the Results found no significant glycogen-synthesis benefit in either the high- or low-carbohydrate subgroup, and the Discussion says the analysis does not establish that a benefit occurs only at lower carbohydrate intakes. The cited amounts are supported; the exclusive condition is not. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Premisecitation
Consuming glucose and fructose during the initial 4 h and again at 15 h of recovery from exhaustive exercise resulted in a notable increase in cycling performance capacity, ~27% longer compared with glucose alone.
“Gray et al. [34] reported that consuming glucose and fructose during the initial 4 h and again at 15 h of recovery from exhaustive exercise resulted in a notable increase in cycling performance capacity, ~ 27% longer compared with glucose alone.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [34] Gray EA, et al. Postexercise glucose-fructose coingestion augments cycling capacity during short-term and overnight recovery from exhaustive exercise, compared with isocaloric glucose. Int J Sport Nutr Exerc Metab. 2020;30(1):54–61. source
The Discussion (page unavailable) reports greater cycling capacity with glucose–fructose than with glucose alone after both 4-hour and 15-hour recoveries. It gives a 27.2% improvement for the 4-hour experiment, but 18.0% for the overnight experiment. The Experimental Trials section says carbohydrate was ingested during the first four hours and cycling capacity was tested at 15 hours; it does not say participants consumed it again at 15 hours. (LLM, conf=0.90)
Experimental — accuracy not yet measured
- Premisecitation
Co-ingestion of carbohydrate (0.86 g·kg−1⋅h−1) with protein (0.27 g·kg−1⋅h−1) did not increase muscle glycogen re-synthesis more than carbohydrate per se when ingested at 0.95 g·kg−1⋅h−1 during short-term post-exercise recovery (≤ 8 h).
“reporting that co-ingestion of carbohydrate (0.86 g·kg−1⋅h−1) with protein (0.27 g·kg−1⋅h−1) did not increase muscle glycogen re-synthesis more than carbohydrate per se when ingested at 0.95 g·kg−1⋅h−1 during short-term post-exercise recovery (≤ 8 h) [86]”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [86] Craven J, et al. The effect of consuming carbohydrate with and without protein on the rate of muscle glycogen re-synthesis during short-term post-exercise recovery: a systematic review and meta-analysis. Sports Med Open. 2021;7(1):9. source
- Premisecitation
Co-ingesting glucose and fructose-based carbohydrates can enhance the recovery of exercise capacity.
“several studies have demonstrated that co-ingesting glucose and fructose-based carbohydrates can enhance the recovery of exercise capacity [29–32]”
Quote in the paperSubstantial claim2 of 4 sources checked- cites [29] Alghannam AF, et al. Impact of muscle glycogen availability on the capacity for repeated exercise in man. Med Sci Sports Exerc. 2016;48(1):123–31. source
- cites [30] McCarthy DG, Spriet LL. Performance effects of carbohydrate ingestion between bouts of intense aerobic interval exercise. Int J Sports Physiol Perform. 2020;15(2):262–7. source
- cites [31] Naderi A, et al. Carbohydrates and endurance exercise: a narrative review of a food first approach. Nutrients. 2023;15(6):1367. source
Section 3 (CHO Ingestion during Exercise; page unavailable) says glucose–fructose beverages may improve endurance capacity compared with glucose alone, but discusses ingestion during exercise, not recovery. Section 4 (Post-Exercise CHO Ingestion; page unavailable) reports that a honey beverage improved performance after a two-hour recovery period versus water, and Section 3 identifies honey as containing both sugars. The review therefore supports a recovery benefit from one mixed-sugar food, but not the broader claim that several studies demonstrated a recovery benefit from glucose–fructose co-ingestion. (LLM, conf=0.84)
Experimental — accuracy not yet measured - cites [32] Burke LM, van Loon LJC, Hawley JA. Postexercise muscle glycogen resynthesis in humans. J Appl Physiol. 2017;122(5):1055–67. source
The 'Type of carbohydrate intake' section reports that glucose and sucrose restored muscle glycogen more effectively than fructose alone. It does not report that co-ingesting glucose- and fructose-based carbohydrates improves recovery of exercise capacity; searches for that combination and for subsequent exercise capacity found no supporting passage. (LLM, conf=0.75)
Experimental — accuracy not yet measured
- Premisecitation
Glucose alone at 1.2 g·kg−1⋅h-1 facilitated a 1.3-1.6 times higher post-exercise muscle glycogen synthesis rate than galactose alone or a glucose + galactose mix.
“glucose alone at the rate of 1.2 g·kg−1⋅h–1 facilitated a 1.3–1.6 times higher post-exercise muscle glycogen synthesis rate than galactose alone or a glucose + galactose mix”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [24] Podlogar T, et al. Postexercise muscle glycogen synthesis with glucose, galactose, and combined galactose-glucose ingestion. Am J Physiol Endocrinol Metab. 2023;325(6):E672–81. source
- Premisecitation
Plant-based proteins such as soy, rice, and pea protein are effective but generally require higher doses (25-40 g) to match the leucine threshold necessary for robust MPS stimulation owing to lower essential amino acid content.
“Plant-based proteins such as soy, rice, and pea protein, while effective [82], generally require higher doses (25–40 g) to match the leucine threshold necessary for robust MPS stimulation owing to lower essential amino acid content [53, 74, 83].”
Quote in the paperSubstantial claim1 of 3 sources checked- cites [53] Pasiakos SM, Lieberman HR, McLellan TM. Effects of protein supplements on muscle damage, soreness and recovery of muscle function and physical performance: a systematic review. Sports Med. 2014;44(5):655–70. source
- cites [74] West S, et al. Nutritional considerations for the vegan athlete. Adv Nutr. 2023;14(4):774–95. source
The Macronutrients > Protein section says some nonanimal proteins may need a higher dose and that differences from animal proteins are often absent at about 30 g. It also notes lower essential amino acid and leucine content. But it does not establish a general 25–40 g requirement for soy, rice, and pea protein or show that this range meets a defined leucine threshold; it says source-specific doses need further research. (LLM, conf=0.87)
Experimental — accuracy not yet measured - cites [83] van der Heijden I, et al. Alternative dietary protein sources to support healthy and active skeletal muscle aging. Nutr Rev. 2023;81(2):206–30. source
- Premisecitation
Drinking water alone may not optimize hydration status, as it has a low BHI value owing to the absence of osmotic nutrient content such as electrolytes, carbohydrate, and protein.
“drinking water alone may not optimize hydration status, as it has a low BHI value owing to the absence of osmotic nutrient content such as electrolytes, carbohydrate, and protein [109]”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [109] Maughan RJ, et al. A randomized trial to assess the potential of different beverages to affect hydration status: development of a beverage hydration index. Am J Clin Nutr. 2016;103(3):717–23. source
The Beverage Hydration Index results show that milk and oral rehydration solution had higher BHIs than still water. The Discussion identifies electrolytes and energy-providing nutrients, including carbohydrate and protein, as possible influences on fluid retention. However, it says the study could not determine the relative effects of individual components, so it does not establish that water’s lower BHI was caused by their absence. The findings concern short-term responses after drinking in a euhydrated state, not an overall optimum for hydration status. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
Sodium bicarbonate supplementation before exercise enhances extracellular buffering capacity when administered at doses of 0.2-0.4 g·kg−1 body mass 1-3 h prior to activity.
“Sodium bicarbonate (NaHCO3) supplementation before exercise is widely recognized for enhancing extracellular buffering capacity when administered at doses of 0.2–0.4 g·kg⁻1 body mass (BM) 1–3 h prior to activity [120].”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [120] Grgic J, et al. International Society of Sports Nutrition position stand: sodium bicarbonate and exercise performance. J Int Soc Sports Nutr. 2022;18(1):1. source
- Premisecitation
Re-establishing water and electrolyte balance during the post-exercise recovery period is important.
“Therefore, re-establishing water and electrolyte balance during the post-exercise recovery period is important [100].”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [100] López-Torres O, et al. Hydration, hyperthermia, glycogen, and recovery: crucial factors in exercise performance—a systematic review and meta-analysis. Nutrients. 2023;15(20):4442. source
The Discussion supports the importance of post-exercise fluid replacement for recovery, particularly for restoring muscle glycogen and avoiding hypohydration before subsequent exercise. The cited passages do not address restoring electrolyte balance, so that part of the claim is unsupported. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
Rehydration strategies between exercise bouts recommend that athletes drink fluids equivalent to 125-150% of their body mass lost during exercise.
“rehydration strategies between exercise bouts recommend that athletes drink fluids equivalent to 125–150% of their body mass lost during exercise [107, 108]”
Quote in the paperSubstantial claim2 of 2 sources checked- cites [107] McCartney D, Desbrow B, Irwin C. The effect of fluid intake following dehydration on subsequent athletic and cognitive performance: a systematic review and meta-analysis. Sports Med Open. 2017;3(1):13. source
The Background reports a recommendation of 1.25–1.50 L per kilogram of body mass lost, equivalent to 125–150% of the loss. It limits that recommendation to cases where the fluid deficit is large and recovery time is short (<12 hours); the citing sentence omits those conditions. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [108] Jardine WT, et al. The effect of pre-exercise hyperhydration on exercise performance, physiological outcomes and gastrointestinal symptoms: a systematic review. Sports Med. 2023;53(11):2111–34. source
The Introduction discusses pre-exercise hyperhydration to offset sweat loss, not rehydration between exercise bouts. Searches for between-bout rehydration and fluid replacement at 125–150% of body mass lost found no passage giving that recommendation. Page numbers were not available in our copy. (LLM, conf=0.75)
Experimental — accuracy not yet measured
- Premisecitation
Oral rehydration solutions, skimmed milk, whole milk, and orange juice had higher beverage hydration index values compared with water.
“finding oral rehydration solutions, skimmed milk, whole milk, and orange juice had higher BHI values compared with water”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [109] Maughan RJ, et al. A randomized trial to assess the potential of different beverages to affect hydration status: development of a beverage hydration index. Am J Clin Nutr. 2016;103(3):717–23. source
- Premisecitation
Delaying post-exercise carbohydrate ingestion by 2 h can lead to reduced muscle glycogen concentrations 4 h after exercise compared with immediate ingestion.
“delaying post-exercise carbohydrate ingestion by 2 h can lead to reduced muscle glycogen concentrations 4 h after exercise compared with immediate ingestion [13]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [13] Ivy JL, et al. Muscle glycogen synthesis after exercise: effect of time of carbohydrate ingestion. J Appl Physiol (1985). 1988;64(4):1480–5. source
- Premisecitation
Ingesting 90 g of carbohydrate in a 2:1 ratio of glucose to fructose during a 4-h post-exercise recovery phase did not enhance muscle glycogen resynthesis compared with glucose alone.
“finding that ingesting 90 g of carbohydrate (~ 1.2 g·kg⁻1·h⁻1) in a 2:1 ratio of glucose to fructose during a 4-h post-exercise recovery phase did not enhance muscle glycogen resynthesis compared with glucose alone”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [21] Wallis GA, et al. Postexercise muscle glycogen synthesis with combined glucose and fructose ingestion. Med Sci Sports Exerc. 2008;40(10):1789–94. source
- Interpretationnone given
Evidence supports the addition of protein to suboptimal carbohydrate intake for enhanced recovery.
“with evidence supporting the addition of protein to suboptimal carbohydrate intake for enhanced recovery”
Quote in the paperNot a substantial claim - Premisecitation
Ingestion of glucose alone increases muscle glycogen levels significantly more than fructose alone.
“Early research demonstrated that ingestion of glucose alone increases muscle glycogen levels significantly more than fructose alone [19, 20].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [19] Blom PC, et al. Effect of different post-exercise sugar diets on the rate of muscle glycogen synthesis. Med Sci Sports Exerc. 1987;19(5):491–6. source
- cites [20] Van Den Bergh AJ, et al. Muscle glycogen recovery after exercise during glucose and fructose intake monitored by 13C-NMR. J Appl Physiol (1985). 1996;81(4):1495–500. source
- Premisecitation
Contemporary guidelines recommend ingesting 1-1.2 g·kg−1⋅h−1 of carbohydrate in the initial 4-h post-exercise window.
“contemporary guidelines recommend ingesting 1–1.2 g·kg−1⋅h−1 of carbohydrate in the initial 4-h post-exercise window [12]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [12] Thomas DT, Erdman KA, Burke LM. American College of Sports Medicine joint position statement. Nutrition and athletic performance. Med Sci Sports Exerc. 2016;48(3):543–68. source
- Interpretationreasoning
Evidence supports the tailored use of these nutritional strategies, particularly for athletes managing tight competition/training schedules.
“Evidence supports the tailored use of these nutritional strategies, particularly for athletes managing tight competition/training schedules.”
Quote in the paperSubstantial claim- Rests on an assumption: The findings from controlled laboratory studies of recovery nutrition are applicable to athletes in real-world competition and training settings with short recovery periods.
- Premisecitation
Muscle glycogen demonstrates a pronounced affinity for restoration during the initial 2 h window following exercise, independent of insulin's influence.
“Muscle glycogen demonstrates a pronounced affinity for restoration during the initial 2 h window following exercise, a process that notably occurs independent of insulin’s influence [10].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [10] Ivy JL, Kuo CH. Regulation of GLUT4 protein and glycogen synthase during muscle glycogen synthesis after exercise. Acta Physiol Scand. 1998;162(3):295–304. source
- Interpretationnone given
Creatine, caffeine, and sodium bicarbonate supplementation may improve post-exercise recovery and subsequent exercise performance in certain scenarios.
“While creatine, caffeine, and sodium bicarbonate supplementation may improve post-exercise recovery and subsequent exercise performance in certain scenarios, their intake should be personalized to accelerate recovery for athletes preparing for the next training session or competition.”
Quote in the paperNot a substantial claim - Premisecitation
Whey protein has been repeatedly demonstrated to enhance MPS more effectively than casein or soy protein owing to its rapid absorption kinetics and high essential amino acid content.
“Whey protein, a fast-digesting and leucine-rich source, has been repeatedly demonstrated to enhance MPS more effectively than casein or soy protein owing to its rapid absorption kinetics and high essential amino acid content [81].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [81] Tang JE, et al. Ingestion of whey hydrolysate, casein, or soy protein isolate: effects on mixed muscle protein synthesis at rest and following resistance exercise in young men. J Appl Physiol (1985). 2009;107(3):987–92. source
- Premisecitation
Ingesting high-GI carbohydrates at a dose of 10 g·kg-1·24 h-1 significantly enhanced post-exercise muscle glycogen restoration compared with low glycemic index carbohydrates (~106 versus 72 mmol·kg−1 wet weight) over a 24-h recovery period.
“research has shown that ingesting high-GI carbohydrates at a dose of 10 g·kg–1·24 h–1 significantly enhanced post-exercise muscle glycogen restoration compared with low glycemic index carbohydrates (~ 106 versus 72 mmol·kg⁻1 wet weight, for high- and low-GI, respectively) over a 24-h recovery period [27]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [27] Burke LM, Collier GR, Hargreaves M. Muscle glycogen storage after prolonged exercise: effect of the glycemic index of carbohydrate feedings. J Appl Physiol (1985). 1993;75(2):1019–23. source
- Premisecitation
Co-ingesting protein with carbohydrate during recovery between two bouts of endurance exercise has shown small to moderate effects on subsequent performance compared with carbohydrate alone (e.g., improvements of ~1.6% in mean power output during cycling time trials and 0.6% in competitive running performance).
“co-ingesting protein with carbohydrate during recovery between two bouts of endurance exercise has shown small to moderate effects on subsequent performance compared with carbohydrate alone (e.g., improvements of ~ 1.6% in mean power output during cycling time trials and 0.6% in competitive running performance [87]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [87] McCartney D, Desbrow B, Irwin C. Post-exercise ingestion of carbohydrate, protein and water: a systematic review and meta-analysis for effects on subsequent athletic performance. Sports Med. 2017;48(2):379–408. source
- Premisecitation
Liver glycogen stores are depleted by approximately 40-60% during moderate to high-intensity exercise sessions that extend beyond 90 min without carbohydrate ingestion.
“Liver glycogen stores are depleted by approximately 40–60% during moderate to high-intensity exercise sessions that extend beyond 90 min without carbohydrate ingestion [23].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [23] Casey A, et al. Effect of carbohydrate ingestion on glycogen resynthesis in human liver and skeletal muscle, measured by (13)C MRS. Am J Physiol Endocrinol Metab. 2000;278(1):E65-75. source
- Premisecitation
Carbohydrate ingestion during exercise can reduce or even completely suppress liver glycogen breakdown, thereby improving subsequent recovery.
“While carbohydrate ingestion during exercise does not substantially affect muscle glycogen utilization [48, 49], it can reduce or even completely suppress liver glycogen breakdown, thereby improving subsequent recovery [49, 50].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [49] Gonzalez JT, et al. Ingestion of glucose or sucrose prevents liver but not muscle glycogen depletion during prolonged endurance-type exercise in trained cyclists. Am J Physiol Endocrinol Metab. 2015;309(12):E1032–9. source
- cites [50] Jeukendrup AE, et al. Carbohydrate ingestion can completely suppress endogenous glucose production during exercise. Am J Physiol. 1999;276(4):E672–83. source
- Premisecitation
The addition of either fructose or galactose to maltodextrin following exercise significantly enhanced the rate of hepatic glycogen synthesis compared with a combination of maltodextrin and glucose.
“it was observed that the addition of either fructose or galactose to maltodextrin following exercise significantly enhanced the rate of hepatic glycogen synthesis compared with a combination of maltodextrin and glucose [28]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [28] Décombaz J, et al. Fructose and galactose enhance postexercise human liver glycogen synthesis. Med Sci Sports Exerc. 2011;43(10):1964–71. source
- Premisecitation
The maltodextrin-fructose combination increased subsequent endurance running capacity by ~33% over the maltodextrin-glucose mix.
“They found that the maltodextrin–fructose combination increased subsequent endurance running capacity by ~ 33% over the maltodextrin–glucose mix, highlighting the potential of glucose–fructose to enhance endurance capacity.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [33] Maunder E, Podlogar T, Wallis GA. Postexercise fructose-maltodextrin ingestion enhances subsequent endurance capacity. Med Sci Sports Exerc. 2018;50(5):1039–45. source
- Interpretationcitation
Combining protein with carbohydrates during recovery periods shorter than 24 h likely has a small, but positive, effect on performance, ranging from 0.6 to 1.6%.
“combining protein with carbohydrates during recovery periods shorter than 24 h likely has a small, but positive, effect on performance, ranging from 0.6 to 1.6% [87]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [87] McCartney D, Desbrow B, Irwin C. Post-exercise ingestion of carbohydrate, protein and water: a systematic review and meta-analysis for effects on subsequent athletic performance. Sports Med. 2017;48(2):379–408. source
- Premisecitation
A threshold increase of 4-6 mmol/L for circulating HCO3− levels determines the ergogenic potential of NaHCO3 supplementation.
“De Oliveira et al. [121] established a threshold increase of 4–6 mmol/L for circulating HCO3⁻ levels to determine the ergogenic potential of NaHCO3 supplementation.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [121] de Oliveira LF, et al. Extracellular buffering supplements to improve exercise capacity and performance: a comprehensive systematic review and meta-analysis. Sports Med. 2022;52(3):505–26. source
- Premisecitation
Sodium bicarbonate supplementation before exercise can improve high-intensity exercise performance lasting approximately 30 s to 10 min.
“This strategy can improve high-intensity exercise performance lasting approximately 30 s to 10 min [121].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [121] de Oliveira LF, et al. Extracellular buffering supplements to improve exercise capacity and performance: a comprehensive systematic review and meta-analysis. Sports Med. 2022;52(3):505–26. source
- Classified as probably not a substantial claim. 3
- May combine two claims. 13
Classified as probably not a substantial claim.
PremisecitationAthletes engaged in power-based sports are advised to ingest 1.7-2.2 g·kg-1 protein.
“while those engaged in power-based sports are advised to ingest 1.7–2.2 g·kg–1 [73]”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [73] Chapman S, et al. Does protein supplementation support adaptations to arduous concurrent exercise training? A systematic review and meta-analysis with military based applications. Nutrients. 2021;13(5):1416. source
The Discussion (§4.1; page not provided) calls 1.7–2.2 g·kg−1·day−1 a current recommendation in the context of arduous concurrent training. It does not identify that range as advice specifically for athletes in power-based sports; §4.2 also discusses the range for periods of intense or high-volume endurance training. (LLM, conf=0.85)
Experimental — accuracy not yet measured
Classified as probably not a substantial claim.
PremisecitationA pre-sleep protein dose of ≥40 g has been recommended to sustain MPS rates and minimize overnight muscle protein breakdown.
“a pre-sleep protein dose of ≥ 40 g has been recommended to sustain MPS rates and minimize overnight muscle protein breakdown [75, 76]”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [75] Res PT, et al. Protein ingestion before sleep improves postexercise overnight recovery. Med Sci Sports Exerc. 2012;44(8):1560–9. source
- cites [76] Trommelen J, et al. Presleep dietary protein-derived amino acids are incorporated in myofibrillar protein during postexercise overnight recovery. Am J Physiol Endocrinol Metab. 2018;314(5):E457-e467. source
The Discussion (page unavailable) reports that 40 g of casein before sleep increased overnight muscle protein synthesis in previous work, while 30 g did not increase myofibrillar protein synthesis in this study. It calls for research to identify the maximal effective dose; it does not recommend a ≥40 g threshold or show that this dose minimizes overnight muscle protein breakdown. (LLM, conf=0.85)
Experimental — accuracy not yet measured
May combine two claims.
InterpretationcitationCo-ingestion of glucose and fructose-based carbohydrates during the post-exercise recovery phase is likely more beneficial than other carbohydrate sources, given its superior efficacy in faster gastrointestinal absorption and glycogen stores and its association with reduced gastrointestinal discomfort when an optimal carbohydrate dosage of 1-1.2 g·kg−1⋅h−1 is consumed.
“it is inferred that the co-ingestion of glucose and fructose-based carbohydrates during the post-exercise recovery phase is likely more beneficial than other carbohydrate sources, given its superior efficacy in faster gastrointestinal absorption and glycogen stores and its association with reduced gastrointestinal discomfort when an optimal carbohydrate dosage of 1–1.2 g·kg−1⋅h−1 is consumed [18]”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [18] Podlogar T, Wallis GA. New horizons in carbohydrate research and application for endurance athletes. Sports Med. 2022;52(Suppl 1):5–23. source
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured
Classified as probably not a substantial claim.
PremisecitationEndurance athletes are recommended to consume ~1.2-1.8 g·kg-1 of high-quality protein.
“Endurance athletes are recommended to consume ~ 1.2–1.8 g·kg–1 of high-quality protein [69–72]”
Quote in the paperSubstantial claim2 of 4 sources checked- cites [69] Tarnopolsky M. Protein requirements for endurance athletes. Nutrition. 2004;20(7–8):662–8. source
- cites [70] Kato H, et al. Protein requirements are elevated in endurance athletes after exercise as determined by the indicator amino acid oxidation method. PLoS ONE. 2016;11(6): e0157406. source
The Discussion reports earlier recommendations of 1.2–1.4 g/kg/day for endurance athletes and this study’s recommended intake of 1.83 g/kg/day, supporting the approximate endpoints. It does not recommend a single 1.2–1.8 g/kg/day range of high-quality protein; the 1.83 estimate comes from a specific controlled-training and post-exercise setting. No page numbers are available in our copy. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [71] Bandegan A, et al. Indicator amino acid oxidation protein requirement estimate in endurance-trained men 24 h postexercise exceeds both the EAR and current athlete guidelines. Am J Physiol Endocrinol Metab. 2019;316(5):E741-e748. source
The Introduction (page unavailable) reports recommendations of 1.2–1.6 g·kg⁻¹·day⁻¹ for endurance-trained individuals. The Discussion (page unavailable) describes 1.8 g·kg⁻¹·day⁻¹ as typical intake, not a recommendation; the cited passages also do not specify high-quality protein. (LLM, conf=0.90)
Experimental — accuracy not yet measured - cites [72] Wooding DJ, et al. Increased protein requirements in female athletes after variable-intensity exercise. Med Sci Sports Exerc. 2017;49(11):2297–304. source
May combine two claims.
InterpretationcitationCurrent research suggests that glucose and glucose-derived carbohydrates, with or without the addition of fructose, are the most effective sources for replenishing post-exercise muscle glycogen within a recovery window ≤ 8 h, and that addition of monosaccharide galactose results in inferior replenishment rates.
“current research suggests that glucose and glucose-derived carbohydrates, with or without the addition of fructose, are the most effective sources for replenishing post-exercise muscle glycogen within a recovery window ≤ 8 h, and that addition of monosaccharide galactose results in inferior replenishment rates [24]”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [24] Podlogar T, et al. Postexercise muscle glycogen synthesis with glucose, galactose, and combined galactose-glucose ingestion. Am J Physiol Endocrinol Metab. 2023;325(6):E672–81. source
May combine two claims.
PremisecitationThe optimal dose of protein for post-exercise recovery is 20-40 g of high-quality protein consumed after exercise, which maximizes MPS rates for several hours (3-4 h), with the exact dose dependent on muscle mass involved during exercise.
“research suggesting that 20–40 g of high-quality protein consumed after exercise maximizes MPS rates for several hours (i.e., 3–4 h), the exact dose dependent on muscle mass involved during exercise [56–58]”
Quote in the paperSubstantial claim3 of 3 sources checked- cites [56] Churchward-Venne TA, Burd NA, Phillips SM. Nutritional regulation of muscle protein synthesis with resistance exercise: strategies to enhance anabolism. Nutr Metab (Lond). 2012;9(1):40. source
The Conclusions (page unavailable) recommend about 20–25 g of rapidly absorbed protein to maximize post-exercise MPS in young healthy individuals. The ‘Leucine as a nutrient signal’ section (page unavailable) reports that 40 g did not increase MPS beyond 20 g in young men; it does not establish a 20–40 g optimal range or make the dose dependent on muscle mass exercised. The ‘window of anabolic potential’ section says the amino-acid-mediated increase lasts a few hours at most, but does not establish the stated 3–4-hour duration. (LLM, conf=0.89)
Experimental — accuracy not yet measured - cites [57] Macnaughton LS, et al. The response of muscle protein synthesis following whole-body resistance exercise is greater following 40 g than 20 g of ingested whey protein. Physiol Rep. 2016;4(15):e12893. source
The Introduction recommends about 20–25 g after leg-only resistance exercise, while the Discussion reports that 40 g produced greater MPS than 20 g after whole-body exercise in young resistance-trained men. The Discussion suggests that the amount of muscle activated may affect the effective dose, but explicitly says the study cannot determine the dose that maximizes MPS. It measured recovery over five hours, not a specified 3–4-hour period. (LLM, conf=0.90)
Experimental — accuracy not yet measured - cites [58] Moore DR, et al. Ingested protein dose response of muscle and albumin protein synthesis after resistance exercise in young men. Am J Clin Nutr. 2009;89(1):161–8. source
The Abstract and Discussion report that 20 g of high-quality protein maximized muscle protein synthesis after leg-based resistance exercise in six young men; the study measured synthesis over four hours. They do not establish that the optimal dose varies with the muscle mass exercised, and the Results found no greater response to 40 g than to 20 g. (LLM, conf=0.88)
Experimental — accuracy not yet measured
May combine two claims.
InterpretationcitationCo-ingestion of glucose with fructose is preferred owing to reduced gastrointestinal complaints and the beneficial effect on liver glycogen replenishment.
“Nevertheless, co-ingestion of glucose with fructose is preferred owing to reduced gastrointestinal complaints and the beneficial effect on liver glycogen replenishment, as discussed below [18, 22, 26]”
Quote in the paperSubstantial claim1 of 3 sources checked- cites [18] Podlogar T, Wallis GA. New horizons in carbohydrate research and application for endurance athletes. Sports Med. 2022;52(Suppl 1):5–23. source
- cites [22] Trommelen J, et al. Fructose coingestion does not accelerate postexercise muscle glycogen repletion. Med Sci Sports Exerc. 2016;48(5):907–12. source
- cites [26] Gonzalez JT, et al. Liver glycogen metabolism during and after prolonged endurance-type exercise. Am J Physiol Endocrinol Metab. 2016;311(3):E543–53. source
May combine two claims.
PremisecitationLiver glycogen resynthesis is inherently slower than that of muscle, possibly owing to its higher rate of glycogen turnover and/or distinct glycogen synthesis pathways that are contingent on hormonal fluctuations.
“Moreover, liver glycogen resynthesis is inherently slower than that of muscle, possibly owing to its higher rate of glycogen turnover and/or distinct glycogen synthesis pathways that are contingent on hormonal fluctuations (notably insulin, glucagon, and epinephrine) [45, 47].”
Quote in the paperSubstantial claim2 of 2 sources checked- cites [45] Gonzalez JT, Wallis GA. Carb-conscious: the role of carbohydrate intake in recovery from exercise. Curr Opin Clin Nutr Metab Care. 2021;24(4):364–71. source
In “Understanding liver glycogen metabolism cannot be simply extrapolated from evidence collection on muscle glycogen metabolism” (page not provided), the paper describes different post-exercise repletion patterns: liver repletion is slower in the first two hours than in hours 2–5, while muscle repletion is fastest early. It also describes substantial liver glycogen turnover and hormonal regulation, but does not establish that liver resynthesis is inherently slower than muscle resynthesis, that liver turnover is higher than muscle turnover, or that distinct synthesis pathways explain the difference. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [47] Gonzalez JT, et al. Glucose plus fructose ingestion for post-exercise recovery-greater than the sum of its parts? Nutrients. 2017;9(4):344. source
Section 3.2 suggests that liver glycogen stores may take longer than muscle stores to recover after exercise, but it does not say liver resynthesis is inherently slower. It attributes the possible difference to post-exercise handling of glucose, not higher glycogen turnover. Sections 5.2 and 2 describe distinct liver synthesis pathways and insulin regulation, but do not establish the claimed explanation involving fluctuations in insulin, glucagon, and epinephrine. Page numbers are unavailable in our copy. (LLM, conf=0.86)
Experimental — accuracy not yet measured
May combine two claims.
InterpretationcitationCo-ingestion of carbohydrates and protein during post-exercise may confer additional benefits, including positive nitrogen balance leading to increased whole-body muscle protein synthesis, increased protein content related to mitochondrial biogenesis, reduced muscle damage markers, and accelerated post-exercise rehydration.
“it may confer additional benefits, including positive nitrogen balance leading to increased whole-body muscle protein synthesis [93], increased protein content related to mitochondrial biogenesis [94], reduced muscle damage markers [95], and accelerated post-exercise rehydration [96]”
Quote in the paperSubstantial claim3 of 3 sources checked- cites [93] Churchward-Venne TA, et al. Dose-response effects of dietary protein on muscle protein synthesis during recovery from endurance exercise in young men: a double-blind randomized trial. Am J Clin Nutr. 2020;112(2):303–17. source
The Discussion (page unavailable) reports that whole-body net protein balance was negative with carbohydrate alone but positive after protein co-ingestion. The Results also report higher myofibrillar protein synthesis with 30 or 45 g of protein. The paper does not establish that positive whole-body balance leads to increased muscle protein synthesis; its Discussion cautions that whole-body protein metabolism is not necessarily reflective of the skeletal-muscle response. The other benefits in the sentence have separate citations and are not assessed here. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [94] Hansen M, et al. Supplement with whey protein hydrolysate in contrast to carbohydrate supports mitochondrial adaptations in trained runners. J Int Soc Sports Nutr. 2020;17(1):46. source
- cites [95] Huang WC, et al. Whey protein improves marathon-induced injury and exercise performance in elite track runners. Int J Med Sci. 2017;14(7):648–54. source
The Discussions report lower CK, LDH and AST after the marathon in athletes given whey protein than in the placebo group, supporting the cited point about reduced muscle-damage markers. However, the Methods (Experimental design) describe whey protein versus maltodextrin, not carbohydrate–protein co-ingestion, so the study does not establish that benefit for the combination. (LLM, conf=0.86)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationMilk-based beverages have led to greater exercise capacity in subsequent exercise performance compared with both noncaloric and energy-matched beverages, likely due to simultaneously increasing glycogen resynthesis and stimulating muscle protein synthesis.
“Milk-based beverages have also led to greater exercise capacity in subsequent exercise performance when compared with both noncaloric and energy-matched beverages, likely due to simultaneously increasing glycogen resynthesis and stimulating muscle protein synthesis [114].”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [114] Russo I, et al. Systematic literature review: the effect of dairy milk on markers of recovery optimisation in response to endurance exercise. Int J sports Sci. 2019:69–85. source
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationAdministering NaHCO3 within approximately <30 min following exercise can restore extracellular acid-base balance during a 75-90 min recovery period between two bouts of exercise and may improve subsequent exercise performance.
“research has shown that administering NaHCO3 within approximately < 30 min following exercise can restore extracellular acid–base balance during a 75–90 min recovery period between two bouts of exercise and may improve subsequent exercise performance [129, 130]”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [129] Gough LA, et al. Ingestion of sodium bicarbonate (NaHCO3) following a fatiguing bout of exercise accelerates postexercise acid-base balance recovery and improves subsequent high-intensity cycling time to exhaustion. Int J Sport Nutr Exerc Metab. 2017;27(5):429–38. source
- cites [130] Gough LA, et al. Post-exercise supplementation of sodium bicarbonate improves acid base balance recovery and subsequent high-intensity boxing specific performance. Front Nutr. 2019;6:155. source
May combine two claims.
PremisecitationExercising in a dehydrated state negatively affects both performance and health.
“Exercising in a dehydrated state is well-established to negatively affect both performance and health [97, 98].”
Quote in the paperSubstantial claim2 of 2 sources checked- cites [97] Lorenzo I, Serra-Prat M, Yébenes JC. The role of water homeostasis in muscle function and frailty: a review. Nutrients. 2019;11(8):1857. source
Section 7 (Dehydration in the Elderly; page unavailable) links dehydration with reduced muscle strength and adverse health outcomes in older adults. Section 10 (Water’s Role in Metabolic Muscle Function; page unavailable) says water loss can affect muscle function. Neither establishes that exercising while dehydrated negatively affects both performance and health, particularly as a well-established general finding. (LLM, conf=0.84)
Experimental — accuracy not yet measured - cites [98] Maughan RJ, Shirreffs SM. Dehydration and rehydration in competative sport. Scand J Med Sci Sports. 2010;20(Suppl 3):40–7. source
The Summary (page not supplied) says dehydration can impair performance and pose a health risk, especially during or after exercise in warm climates. It qualifies this finding: dehydration must be sufficiently severe, and low levels are well tolerated in cool environments. The citing sentence omits those limits. (LLM, conf=0.88)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationProtein ingestion after exercise promotes muscle protein synthesis, reduces muscle protein breakdown, and facilitates muscle repair and adaptation following exercise-induced damage.
“Protein ingestion after exercise is considered one of the pillars of recovery owing to its role in promoting muscle protein synthesis (MPS), reducing muscle protein breakdown, and facilitating muscle repair and adaptation following exercise-induced damage [51–54].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [51] Moore DR, et al. Beyond muscle hypertrophy: why dietary protein is important for endurance athletes. Appl Physiol Nutr Metab. 2014;39(9):987–97. source
- cites [52] Doering TM, et al. Postexercise dietary protein strategies to maximize skeletal muscle repair and remodeling in masters endurance athletes: a review. Int J Sport Nutr Exerc Metab. 2016;26(2):168–78. source
- cites [53] Pasiakos SM, Lieberman HR, McLellan TM. Effects of protein supplements on muscle damage, soreness and recovery of muscle function and physical performance: a systematic review. Sports Med. 2014;44(5):655–70. source
- cites [54] Tipton KD, Wolfe RR. Protein and amino acids for athletes. J Sports Sci. 2004;22(1):65–79. source
May combine two claims.
PremisecitationEffective post-exercise recovery is critical for restoring physiological homeostasis, repairing muscle damage, replenishing energy stores, and facilitating adaptations that enhance athletic performance.
“Effective post-exercise recovery is critical for restoring physiological homeostasis, repairing muscle damage, replenishing energy stores, and facilitating adaptations that enhance athletic performance [1].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [1] Kenttä G, Hassmén P. Overtraining and recovery. A conceptual model. Sports Med. 1998;26(1):1–16. source
May combine two claims.
InterpretationcitationAlthough high-GI carbohydrate ingestion leads to higher glycogen content after 24 h of recovery, during very short recovery periods the total carbohydrate dose appears more important than the GI.
“although high-GI carbohydrate ingestion leads to higher glycogen content after 24 h of recovery [27], during very short recovery periods the total carbohydrate dose appears more important than the GI”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [27] Burke LM, Collier GR, Hargreaves M. Muscle glycogen storage after prolonged exercise: effect of the glycemic index of carbohydrate feedings. J Appl Physiol (1985). 1993;75(2):1019–23. source
May combine two claims.
InterpretationreasoningMixed results suggest that the type of exercise, its intensity and duration, the specific carbohydrate dosages used, and the glycogen depletion protocols might play critical roles in determining the efficacy of carbohydrate supplementation.
“These mixed results suggest that the type of exercise, its intensity and duration, the specific carbohydrate dosages used, and the glycogen depletion protocols might play critical roles in determining the efficacy of carbohydrate supplementation”
Quote in the paperSubstantial claim
The paper relies on this without support.
The findings from controlled laboratory studies of recovery nutrition are applicable to athletes in real-world competition and training settings with short recovery periods.
“Evidence supports the tailored use of these nutritional strategies, particularly for athletes managing tight competition/training schedules.”
The paper relies on this without support.
Performance improvements measured in laboratory time trials or capacity tests translate into competitive performance outcomes.
“However, even a 1% improvement can be critical in elite sports, potentially making the difference between finishing fourth and securing a podium position in Olympic competitions [88].”
The paper relies on this without support.
The cited studies' participants and protocols are sufficiently comparable to synthesize into general recommendations for athletes.
“These discrepancies may be attributed to interindividual variations in training status and genetic factors, as well as differences in recovery durations, glycogen depletion protocols, performance tests, amounts and types of protein ingested, and methods of nutrient provision during recovery.”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Post-exercise fluid replacement ranges differ
MajorThe hydration section recommends replacing 125-150% of body mass lost during exercise, while Table 1 advises replacing 150-200% of lost sweat. Although the ranges meet at 150%, they give different recommended amounts above and below that point.
“Replacement of 150–200% of lost sweat within 4–8 h is advised for effective rehydration”
“rehydration strategies between exercise bouts recommend that athletes drink fluids equivalent to 125–150% of their body mass lost during exercise [107, 108].”
Strength-athlete protein recommendation differs from the main text
MinorTable 2 recommends 1.2-1.8 g·kg-1 daily for strength/power athletes, whereas the protein section recommends 1.7-2.2 g·kg-1 for athletes in power-based sports. The table substitutes the endurance-athlete range for the higher power-sport range stated in the text.
“followed by a total daily intake of 1.2–1.8 g·kg–1 for endurance athletes and intake of 1.2–1.8 g·kg–1 for strength power athletes”
“Endurance athletes are recommended to consume ~ 1.2–1.8 g·kg–1 of high-quality protein [69–72], while those engaged in power-based sports are advised to ingest 1.7–2.2 g·kg–1 [73].”
Cites
Exercise Metabolism and the Molecular Regulation of Skeletal Muscle Adaptation
Egan, B., & Zierath, J. R. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2012.12.012 · Cited by 2,084 · cited 1× · see citing works
“Beyond RONS, exercise adaptations are also regulated by contraction-induced changes in mechanical strain, adenosine triphosphate (ATP) turnover, calcium flux, redox balance, and intracellular oxygen pressure [215].”
Monitoring Training Load to Understand Fatigue in Athletes
Halson, S. L. (2014) · Sports Medicine · doi:10.1007/s40279-014-0253-z · Cited by 1,953 · cited 1× · see citing works
“In addition, managing fatigue and training load is essential for athletes aiming to achieve peak performance and prevent overtraining [1–3].”
Romijn, J. A., Coyle, E. F., Sidossis, L. S., Gastaldelli, A., Horowitz, J. F., Endert, E., & Wolfe, R. R. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.265.3.e380 · Cited by 1,747 · cited 1× · see citing works
“IMTG stores are used as an energy source mainly during early stages of endurance exercise, with the reliance on them diminishing as exercise duration extends in favor of plasma-derived substrate oxidation [175].”
Antioxidants prevent health-promoting effects of physical exercise in humans
Ristow, M., Zarse, K., Oberbach, A., Klöting, N., Birringer, M., Kiehntopf, M., Stumvoll, M., Kahn, C. R., & Blüher, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903485106 · Cited by 1,582 · cited 1× · see citing works
“For example, two human studies showing a blunting of some markers of training adaptations also had the largest sample sizes [211, 212], whereas a study showing no statistical effect of vitamin C on increases in V O 2max reported increases of 10.8% in the supplementation group ( n = 5) and an…”
InfluentialNutrition and Athletic Performance
(2016) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000852 · Cited by 1,305 · cited 1× · see citing works
“Although some muscle glycogen can be repleted in the absence of food ingestion [11], contemporary guidelines recommend ingesting 1–1.2 g·kg −1 ⋅ h −1 of carbohydrate in the initial 4-h post-exercise window [12].”
InfluentialMuscle glycogen utilization during prolonged strenuous exercise when fed carbohydrate
Coyle, E. F., Coggan, A. R., Hemmert, M. K., & Ivy, J. L. (1986) · Journal of Applied Physiology · doi:10.1152/jappl.1986.61.1.165 · Cited by 1,022 · cited 1× · see citing works
“While carbohydrate ingestion during exercise does not substantially affect muscle glycogen utilization [48, 49], it can reduce or even completely suppress liver glycogen breakdown, thereby improving subsequent recovery [49, 50].”
Tang, J. E., Moore, D. R., Kujbida, G. W., Tarnopolsky, M. A., & Phillips, S. M. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00076.2009 · Cited by 998 · see citing works
Carbohydrates for training and competition
Burke, L. M., Hawley, J. A., Wong, S. H. S., & Jeukendrup, A. E. (2011) · Journal of Sports Sciences · doi:10.1080/02640414.2011.585473 · Cited by 985 · cited 1× · see citing works
“Complete replenishment of muscle glycogen stores typically unfolds over a 24–36 h period post-exercise, provided that 7–12 g·kg −1 carbohydrate are consumed per day [15–18].”
Moore, D. R., Robinson, M. J., Fry, J. L., Tang, J. E., Glover, E. I., Wilkinson, S. B., Prior, T., Tarnopolsky, M. A., & Phillips, S. M. (2009) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.26401 · Cited by 973 · cited 1× · see citing works
“The optimal dose of protein for post-exercise recovery has been extensively studied, with research suggesting that 20–40 g of high-quality protein consumed after exercise maximizes MPS rates for several hours (i.e., 3–4 h), the exact dose dependent on muscle mass involved during exercise [56–58].”
Gomez-Cabrera, M.-C., Domenech, E., Romagnoli, M., Arduini, A., Borras, C., Pallardo, F. V., Sastre, J., & Viña, J. (2008) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/87.1.142 · Cited by 844 · cited 1× · see citing works
“…212], whereas a study showing no statistical effect of vitamin C on increases in V O 2max reported increases of 10.8% in the supplementation group ( n = 5) and an increase of 22% in the group ( n = 9) without supplementation (Cohen’s d = − 1.1, [95% confidence interval (CI) − 2.2, 0.04]) [213].”
InfluentialOvertraining and Recovery: A Conceptual Model
Kenttä, G., & Hassmén, P. (1998) · Sports Medicine · doi:10.2165/00007256-199826010-00001 · Cited by 750 · see citing works
Elliott-Sale, K. J., Minahan, C. L., de Jonge, X. A. K. J., Ackerman, K. E., Sipilä, S., Constantini, N. W., Lebrun, C. M., & Hackney, A. C. (2021) · Sports Medicine · doi:10.1007/s40279-021-01435-8 · Cited by 731 · cited 1× · see citing works
“…150% body mass loss from exercise Include electrolytes if food is not also consumed Can assess hydration status through urine color, frequency, and volume or by measuring urine specific gravity and osmolality in the recommendations—a common problem within the sports science literature [217].”
Mountjoy, M., Ackerman, K. E., Bailey, D. M., Burke, L. M., Constantini, N., Hackney, A. C., Heikura, I. A., Melin, A., Pensgaard, A. M., Stellingwerff, T., et al. (2023) · British Journal of Sports Medicine · doi:10.1136/bjsports-2023-106994 · Cited by 724 · cited 1× · see citing works
“Nutritional strategies play a pivotal role in the recovery process by replenishing energy stores, maintaining energy availability [4], and promoting repair mechanisms and adaptive responses to exercise [5, 6].”
Preventing overtraining in athletes in high‐intensity sports and stress/recovery monitoring
Kellmann, M. (2010) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2010.01192.x · Cited by 596 · see citing works
Exercise and oxidative stress: Potential effects of antioxidant dietary strategies in sports
Pingitore, A., Lima, G. P. P., Mastorci, F., Quinones, A., Iervasi, G., & Vassalle, C. (2015) · Nutrition · doi:10.1016/j.nut.2015.02.005 · Cited by 511 · cited 1× · see citing works
“Free radicals produced via aerobic metabolism contribute both to exercise-induced fatigue as well as the adaptive response to exercise [209].”
Areta, J. L., Burke, L. M., Ross, M. L., Camera, D. M., West, D. W. D., Broad, E. M., Jeacocke, N. A., Moore, D. R., Stellingwerff, T., Phillips, S. M., et al. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.244897 · Cited by 495 · cited 3× · see citing works
“Following the initial protein-based meal after exercise, it is advised that subsequent protein-rich meals follow at 3–4 h intervals [55, 66, 67].”
Muscle glycogen synthesis after exercise: effect of time of carbohydrate ingestion
Ivy, J. L., Katz, A. L., Cutler, C. L., Sherman, W. M., & Coyle, E. F. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.64.4.1480 · Cited by 459 · cited 2× · see citing works
“Adapted from [13, 21, 24, 27, 28].”
Physiological and Health Effects of Oral Creatine Supplementation
Terjung, R. L., Clarkson, P. M., Eichner, E. R., Greenhaff, P. L., Hespel, P., Israel, R. G., Kraemer, W. J., Meyer, R. A., Spriet, L. L., Tarnopolsky, M. A., et al. (2000) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200003000-00024 · Cited by 417 · cited 1× · see citing works
“Creatine (α-methyl-guanidinoacetic acid) is a widely used nutritional supplement that has been extensively researched over the past two decades [142].”
Baker, L. B. (2017) · Sports Medicine · doi:10.1007/s40279-017-0691-5 · Cited by 403 · cited 1× · see citing works
“…exercise in a hot or humid environment, athletes may lose more than 2 L of sweat per hour, accompanied by substantial electrolyte, extracellular, and intracellular water loss that may negatively affect processes such as the rate of post-exercise glycogen and muscle protein resynthesis [44, 99].”
Grgic, J., Grgic, I., Pickering, C., Schoenfeld, B. J., Bishop, D. J., & Pedisic, Z. (2020) · British Journal of Sports Medicine · doi:10.1136/bjsports-2018-100278 · Cited by 375 · cited 1× · see citing works
“Caffeine (1,3,7-trimethylxanthine) is one of the most extensively researched performance-enhancing supplements and is known to enhance exercise performance when consumed before [157] and during prolonged exercise [158].”
Paulsen, G., Cumming, K. T., Holden, G., Hallén, J., Rønnestad, B. R., Sveen, O., Skaug, A., Paur, I., Bastani, N. E., Østgaard, H. N., et al. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2013.267419 · Cited by 333 · cited 1× · see citing works
“For example, two human studies showing a blunting of some markers of training adaptations also had the largest sample sizes [211, 212], whereas a study showing no statistical effect of vitamin C on increases in V O 2max reported increases of 10.8% in the supplementation group ( n = 5) and an…”
InfluentialIsomer-Specific Antidiabetic Properties of Conjugated Linoleic Acid
Ryder, J. W., Portocarrero, C. P., Song, X., Cui, L., Yu, M., COMBATSIARIS, T. P., Galuska, D., Bauman, D. E., Barbano, D. M., Charron, M. J., et al. (2001) · Diabetes · doi:10.2337/diabetes.50.5.1149 · Cited by 316 · cited 1× · see citing works
“…and provides some more mechanistical evidence for these findings, namely showing increased muscle glycogen synthase activity with a mixture of isomers ( cis -9 trans -11, cis -10 trans -12), but not with cis -9 trans -11 isomer, suggesting physiological effects are likely isomer-specific [186].”
The effect of caffeine on subsequent sleep: A systematic review and meta-analysis
Gardiner, C., Weakley, J., Burke, L. M., Roach, G. D., Sargent, C., Maniar, N., Townshend, A., & Halson, S. L. (2023) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2023.101764 · Cited by 315 · cited 1× · see citing works
“It is important to note that excessive caffeine intake can lead to adverse effects, including tachycardia, anxiety, headaches, gastrointestinal issues, and a heightened risk of overnight insomnia [172, 173].”
Exercise‐induced muscle damage: What is it, what causes it and what are the nutritional solutions?
Owens, D. J., Twist, C., Cobley, J. N., Howatson, G., & Close, G. L. (2018) · European Journal of Sport Science · doi:10.1080/17461391.2018.1505957 · Cited by 309 · cited 1× · see citing works
“…acid (DHA) are types of fats that have reported anti-inflammatory properties and the capacity for reducing EIMD and enhancing muscle function following exercise [182], providing additional rationale for their recommended use in aiding exercise recovery in a dose-and duration-dependent manner [183].”
Utilization of skeletal muscle triacylglycerol during postexercise recovery in humans
Kiens, B., & Richter, E. A. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.275.2.e332 · Cited by 290 · cited 1× · see citing works
“IMTG are also utilized as a fuel source in the post-exercise recovery window [176].”
Muscle composition in relation to age and sex
Forsberg, A. M., Nilsson, E., Werneman, J., Bergström, J., & Hultman, E. (1991) · Clinical Science · doi:10.1042/cs0810249 · Cited by 282 · cited 1× · see citing works
“Given that creatine metabolism exhibits sex-specific differences [156], there is a need for a better understanding of creatine supplementation’s effects across sex and levels of athletic training.”
Protein and amino acids for athletes
Tipton, K. D., & Wolfe, R. R. (2004) · Journal of Sports Sciences · doi:10.1080/0264041031000140554 · Cited by 274 · cited 1× · see citing works
“Protein ingestion after exercise is considered one of the pillars of recovery owing to its role in promoting muscle protein synthesis (MPS), reducing muscle protein break-down, and facilitating muscle repair and adaptation following exercise-induced damage [51–54].”
West, D. W., Burd, N. A., Coffey, V. G., Baker, S. K., Burke, L. M., Hawley, J. A., Moore, D. R., Stellingwerff, T., & Phillips, S. M. (2011) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.111.013722 · Cited by 264 · cited 1× · see citing works
“Nevertheless, it is commonly recommended to rapidly increase amino acid availability following exercise to maximize MPS rates and promote muscle recovery [55, 64], with numerous studies demonstrating positive effects on recovery in endurance athletes [62, 63, 65].”
Burke, L. M., Collier, G. R., & Hargreaves, M. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.75.2.1019 · Cited by 247 · cited 4× · see citing works
“In summary, although high-GI carbohydrate ingestion leads to higher glycogen content after 24 h of recovery [27], during very short recovery periods the total carbohydrate dose appears more important than the GI.”
InfluentialProtein requirements for endurance athletes
Tarnopolsky, M. (2004) · Nutrition · doi:10.1016/j.nut.2004.04.008 · Cited by 242 · cited 1× · see citing works
“Endurance athletes are recommended to consume ~ 1.2–1.8 g·kg –1 of high-quality protein [69–72], while those engaged in power-based sports are advised to ingest 1.7–2.2 g·kg –1 [73].”
InfluentialPostexercise muscle glycogen resynthesis in humans.
Burke, L. M., van Loon, L. J. C., & Hawley, J. A. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00860.2016 · Cited by 242 · cited 1× · see citing works
“From a performance perspective, several studies have demonstrated that co-ingesting glucose and fructose-based carbohydrates can enhance the recovery of exercise capacity [29–32].”
The Role of Water Homeostasis in Muscle Function and Frailty: A Review
Lorenzo, I., Serra-Prat, M., & Yébenes, J. C. (2019) · Nutrients · doi:10.3390/nu11081857 · Cited by 239 · cited 1× · see citing works
“Exercising in a dehydrated state is well-established to negatively affect both performance and health [97, 98].”
Effect of resistance exercise on free radical production
McBride, J. M., Kraemer, W. J., Triplett-McBride, T., et al. (1998) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199801000-00010 · Cited by 236 · cited 1× · see citing works
“…tart cherry [191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence surrounding tart cherry, beetroot, pomegranate, and vitamin D…”
Impey, S. G., Hearris, M. A., Hammond, K. M., Bartlett, J. D., Louis, J., Close, G. L., & Morton, J. P. (2018) · Sports Medicine · doi:10.1007/s40279-018-0867-7 · Cited by 232 · cited 1× · see citing works
“…caffeine alongside carbohydrates during the initial post-exercise recovery hours may benefit athletes who have multiple competitions in a single day or who employ training sessions with low carbohydrate availability, such as the “sleep low, train low” thought to maximize training adaptations [171].”
Protein Ingestion before Sleep Improves Postexercise Overnight Recovery
RES, P. T., GROEN, B., PENNINGS, B., BEELEN, M., WALLIS, G. A., GIJSEN, A. P., SENDEN, J. M. G., & VAN LOON, L. J. C. (2012) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31824cc363 · Cited by 226 · cited 1× · see citing works
“Considering the extended fasting period during sleep, a pre-sleep protein dose of ≥ 40 g has been recommended to sustain MPS rates and minimize overnight muscle protein breakdown [75, 76].”
Fundamentals of glycogen metabolism for coaches and athletes
Murray, B., & Rosenbloom, C. (2018) · Nutrition Reviews · doi:10.1093/nutrit/nuy001 · Cited by 224 · see citing works
Carbohydrate ingestion can completely suppress endogenous glucose production during exercise
Jeukendrup, A. E., Wagenmakers, A. J. M., Stegen, J. H. C. H., Gijsen, A. P., Brouns, F., & Saris, W. H. M. (1999) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1999.276.4.e672 · Cited by 219 · cited 1× · see citing works
“While carbohydrate ingestion during exercise does not substantially affect muscle glycogen utilization [48, 49], it can reduce or even completely suppress liver glycogen breakdown, thereby improving subsequent recovery [49, 50].”
Fruit-Derived Polyphenol Supplementation for Athlete Recovery and Performance
Bowtell, J., & Kelly, V. (2019) · Sports Medicine · doi:10.1007/s40279-018-0998-x · Cited by 213 · cited 3× · see citing works
“These benefits are likely due to antioxidant effects and have been observed in both trained and untrained populations [203].”
Loenneke, J. P., Loprinzi, P. D., Murphy, C. H., & Phillips, S. M. (2016) · Clinical Nutrition · doi:10.1016/j.clnu.2016.04.002 · Cited by 208 · cited 1× · see citing works
“Following the initial protein-based meal after exercise, it is advised that subsequent protein-rich meals follow at 3–4 h intervals [55, 66, 67].”
Liver glycogen metabolism during and after prolonged endurance-type exercise
Gonzalez, J. T., Fuchs, C. J., Betts, J. A., & van Loon, L. J. C. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00232.2016 · Cited by 206 · cited 2× · see citing works
“Nevertheless, co-ingestion of glucose with fructose is preferred owing to reduced gastrointestinal complaints and the beneficial effect on liver glycogen replenishment, as discussed below [18, 22, 26] (Supplementary Material 1).”
Use of intramuscular triacylglycerol as a substrate source during exercise in humans
van Loon, L. J. C. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00368.2004 · Cited by 205 · cited 1× · see citing works
“Fat is primarily stored as triacylglycerol (TG) in adipose tissue, with smaller amounts inside muscle fibers (intramyocel-lular TG; IMTG) [174].”
The effect of protein timing on muscle strength and hypertrophy: a meta-analysis
Schoenfeld, B. J., Aragon, A. A., & Krieger, J. W. (2013) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-10-53 · Cited by 201 · see citing works
Effect of different post-exercise sugar diets on the rate of muscle glycogen synthesis
BLOM, P. C. S., H??STMARK, A. T., VAAGE, O., KARDEL, K. R., & M??HLUM, S. (1987) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-198710000-00012 · Cited by 198 · cited 2× · see citing works
“This finding aligns with subsequent studies comparing glucose, fructose, and sucrose in 1 g·kg –1 ⋅ h –1 doses during a 4–6 h post-exercise timeframe [19, 23].”
Fluid and electrolyte loss and replacement in exercise
Maughan, R. J. (1991) · Journal of Sports Sciences · doi:10.1080/02640419108729870 · Cited by 191 · cited 1× · see citing works
“Attempts to correct fluid loss induced by exercise should consider the sweat rate, which can vary from 0 to over 2 L·h ⁻ 1 , depending on factors such as environmental conditions, intensity, duration, genetics, fitness level, acclimatization to the environment, and clothing [104, 105].”
Macnaughton, L. S., Wardle, S. L., Witard, O. C., McGlory, C., Hamilton, D. L., Jeromson, S., Lawrence, C. E., Wallis, G. A., & Tipton, K. D. (2016) · Physiological Reports · doi:10.14814/phy2.12893 · Cited by 191 · see citing works
Fluid and electrolyte needs for training, competition, and recovery
Shirreffs, S. M., & Sawka, M. N. (2011) · Journal of Sports Sciences · doi:10.1080/02640414.2011.614269 · Cited by 190 · cited 2× · see citing works
“For example, daily water and sodium losses can vary significantly and be in the range of 4–10 L and 3.5–7.0 g, respectively, in active athletes under heat stress; thus, both need to be replaced to re-establish normal total body water (i.e., achieve euhydration) [106].”
InfluentialChurchward-Venne, T. A., Burd, N. A., & Phillips, S. M. (2012) · Nutrition & Metabolism · doi:10.1186/1743-7075-9-40 · Cited by 186 · cited 1× · see citing works
“The optimal dose of protein for post-exercise recovery has been extensively studied, with research suggesting that 20–40 g of high-quality protein consumed after exercise maximizes MPS rates for several hours (i.e., 3–4 h), the exact dose dependent on muscle mass involved during exercise [56–58].”
Maximizing Cellular Adaptation to Endurance Exercise in Skeletal Muscle
Hawley, J. A., Lundby, C., Cotter, J. D., & Burke, L. M. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.04.014 · Cited by 182 · cited 1× · see citing works
“Nutritional strategies play a pivotal role in the recovery process by replenishing energy stores, maintaining energy availability [4], and promoting repair mechanisms and adaptive responses to exercise [5, 6].”
Creatine for exercise and sports performance, with recovery considerations for healthy populations
Wax, B., Kerksick, C. M., Jagim, A. R., Mayo, J. J., Lyons, B. C., & Kreider, R. B. (2021) · Nutrients · doi:10.3390/nu13061915 · Cited by 182 · cited 1× · see citing works
“It may also mitigate post-exercise inflammation, reducing markers of muscle damage and soreness [146].”
Pasiakos, S. M., Lieberman, H. R., & McLellan, T. M. (2014) · Sports Medicine · doi:10.1007/s40279-013-0137-7 · Cited by 178 · cited 2× · see citing works
“Plant-based proteins such as soy, rice, and pea protein, while effective [82], generally require higher doses (25–40 g) to match the leucine threshold necessary for robust MPS stimulation owing to lower essential amino acid content [53, 74, 83].”
Eccentric exercise-induced muscle damage impairs muscle glycogen repletion
O’Reilly, K., Warhol, M. J., Fielding, R. A., Frontera, W. R., Meredith, C. N., & Evans, W. J. (1987) · Journal of Applied Physiology · doi:10.1152/jappl.1987.63.1.252 · Cited by 169 · cited 1× · see citing works
“This is important because exercise-induced muscle damage (EIMD) can impede muscle glycogen replenishment for up to 10 days [147], suggesting that creatine could facilitate glycogen resynthesis by alleviating EIMD.”
The impact of protein quality on the promotion of resistance exercise-induced changes in muscle mass
Phillips, S. M. (2016) · Nutrition & Metabolism · doi:10.1186/s12986-016-0124-8 · Cited by 168 · cited 1× · see citing works
“Amounts of essential amino acids, and especially leucine content, in protein sources seem to be the strongest predictor of MPS [79, 80].”
Dehydration and rehydration in competative sport
Maughan, R. J., & Shirreffs, S. M. (2010) · Scandinavian Journal of Medicine & Science in Sports · doi:10.1111/j.1600-0838.2010.01207.x · Cited by 167 · cited 1× · see citing works
“Exercising in a dehydrated state is well-established to negatively affect both performance and health [97, 98].”
Thong, F. S. L., Derave, W., Kiens, B., Graham, T. E., Ursø, B., Wojtaszewski, J. F. P., Hansen, B. F., & Richter, E. A. (2002) · Diabetes · doi:10.2337/diabetes.51.3.583 · Cited by 167 · cited 1× · see citing works
“…protein kinase (AMPK), possibly through enhanced activation of the Ca 2+ -calmodulin-dependent protein kinase (CaMK) and the phosphorylation of acetyl-CoA carboxylase (ACC), which could collectively induce translocation of GLUT4 to the cell membrane and promote muscle glucose uptake [162, 163].”
Effects of diet on muscle triglyceride and endurance performance
Starling, R. D., Trappe, T. A., Parcell, A. C., KERR, C. G., Fink, W. J., & COSTILL, D. L. (1997) · Journal of Applied Physiology · doi:10.1152/jappl.1997.82.4.1185 · Cited by 166 · cited 1× · see citing works
“However, their availability does not seem to play a role in performance as interventions aimed at increasing IMTG have resulted in either no differences [177] or worsened [178] performance in exercise trials lasting 20–140 min.”
Bell, P., Walshe, I. H., Davison, G. W., Stevenson, E., & Howatson, G. (2014) · Nutrients · doi:10.3390/nu6020829 · Cited by 166 · cited 2× · see citing works
“Despite reductions in muscle damage and/or inflammation, improvements in performance are not always observed [191, 192].”
Moopanar, T. R., & Allen, D. G. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.083519 · Cited by 165 · cited 1× · see citing works
“Antioxidants have the potential to improve recovery and acute performance by reducing RONS, which impair muscle contractile force primarily through alterations in myofibrillar calcium sensitivity [204].”
McFarlin, B. K., Venable, A. S., Henning, A. L., Sampson, J. N. B., Pennel, K. A. F., Vingren, J. L., & Hill, D. W. (2016) · BBA Clinical · doi:10.1016/j.bbacli.2016.02.003 · Cited by 165 · cited 1× · see citing works
“…[191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence surrounding tart cherry, beetroot, pomegranate, and vitamin D [202, 203].”
Effect of Oral Creatine Supplementation on Human Muscle GLUT4 Protein Content After Immobilization
Eijnde, B. O. '., Ursø, B., Richter, E. A., Greenhaff, P. L., & Hespel, P. (2001) · Diabetes · doi:10.2337/diabetes.50.1.18 · Cited by 162 · cited 1× · see citing works
“Creatine may enhance the abundance of glucose transporter (GLUT) 4, facilitating greater glucose uptake into muscle cells [145].”
Role of submaximal exercise in promoting creatine and glycogen accumulation in human skeletal muscle
Robinson, T. M., Sewell, D. A., Hultman, E., & Greenhaff, P. L. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.2.598 · Cited by 160 · cited 2× · see citing works
“In addition, creatine supplementation may positively affect muscle glycogen storage in the days following glycogen-depleting exercise [144].”
McLeay, Y., Barnes, M. J., Mündel, T., Hurst, S. M., Hurst, R. D., & Stannard, S. R. (2012) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-9-19 · Cited by 160 · cited 1× · see citing works
“…supplements may be effective in reducing EIMD, including fruit extracts such as tart cherry [191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the…”
Effects of endurance exercise training on muscle glycogen accumulation in humans
Greiwe, J. S., Hickner, R. C., Hansen, P. A., Racette, S. B., Chen, M. M., & Holloszy, J. O. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.1.222 · Cited by 147 · see citing works
Restoration of fluid balance after exercise-induced dehydration: effects of food and fluid intake
Maughan, R., Leiper, J. B., & Shirreffs, S. M. (1996) · European Journal of Applied Physiology · doi:10.1007/bf02425493 · Cited by 145 · cited 1× · see citing works
“…that, regardless of beverage choice, similar recovery fluid balance [117, 118] and subsequent exercise performance [118] can be achieved using milk-based formulations, sports drinks, or water along with different solid meals in both males and females, despite varying dietary behaviors [117–119].”
Maughan, R. J., Watson, P., Cordery, P. A., Walsh, N. P., Oliver, S. J., Dolci, A., Rodriguez-Sanchez, N., & Galloway, S. D. (2016) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.115.114769 · Cited by 144 · see citing works
Casey, A., Mann, R., Banister, K., Fox, J., Morris, P. G., Macdonald, I. A., & Greenhaff, P. L. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.278.1.e65 · Cited by 140 · cited 2× · see citing works
“Liver glycogen stores are depleted by approximately 40–60% during moderate to high-intensity exercise sessions that extend beyond 90 min without carbohydrate ingestion [23].”
Nutrient timing revisited: is there a post-exercise anabolic window?
Aragon, A. A., & Schoenfeld, B. J. (2013) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-10-5 · Cited by 139 · cited 1× · see citing works
“While the importance of immediate post-exercise protein intake remains debated in literature [59–61], this controversy largely arises from differences in study designs and varying recovery conditions [62, 63].”
Beyond muscle hypertrophy: why dietary protein is important for endurance athletes
Moore, D. R., Camera, D. M., Areta, J. L., & Hawley, J. A. (2014) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2013-0591 · Cited by 138 · cited 1× · see citing works
“Protein ingestion after exercise is considered one of the pillars of recovery owing to its role in promoting muscle protein synthesis (MPS), reducing muscle protein break-down, and facilitating muscle repair and adaptation following exercise-induced damage [51–54].”
Grgic, J., Pedisic, Z., Saunders, B., Artioli, G. G., Schoenfeld, B. J., McKenna, M. J., Bishop, D. J., Kreider, R. B., Stout, J. R., Kalman, D. S., et al. (2021) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-021-00458-w · Cited by 138 · cited 1× · see citing works
“Sodium bicarbonate (NaHCO 3 ) supplementation before exercise is widely recognized for enhancing extracellular buffering capacity when administered at doses of 0.2–0.4 g·kg ⁻ 1 body mass (BM) 1–3 h prior to activity [120].”
InfluentialBurke, L. M. (2017) · Sports Medicine · doi:10.1007/s40279-017-0687-1 · Cited by 132 · see citing works
Temporal changes in human skeletal muscle and blood lipid composition with fish oil supplementation
McGlory, C., Galloway, S. D. R., Hamilton, D. L., McClintock, C., Breen, L., Dick, J. R., Bell, J. G., & Tipton, K. D. (2014) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2014.03.001 · Cited by 130 · cited 1× · see citing works
“…acid (DHA) are types of fats that have reported anti-inflammatory properties and the capacity for reducing EIMD and enhancing muscle function following exercise [182], providing additional rationale for their recommended use in aiding exercise recovery in a dose-and duration-dependent manner [183].”
Regulation of GLUT4 protein and glycogen synthase during muscle glycogen synthesis after exercise
IVY, J. L., & KUO, C. ‐. (1998) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1998.0302e.x · Cited by 129 · cited 1× · see citing works
“Muscle glycogen demonstrates a pronounced affinity for restoration during the initial 2 h window following exercise, a process that notably occurs independent of insulin’s influence [10].”
Kato, H., Suzuki, K., Bannai, M., & Moore, D. R. (2016) · PLOS ONE · doi:10.1371/journal.pone.0157406 · Cited by 128 · see citing works
Swifter, higher, stronger: What’s on the menu?
Burke, L. M., & Hawley, J. A. (2018) · Science · doi:10.1126/science.aau2093 · Cited by 125 · cited 1× · see citing works
“Nutritional strategies play a pivotal role in the recovery process by replenishing energy stores, maintaining energy availability [4], and promoting repair mechanisms and adaptive responses to exercise [5, 6].”
Polyphenols and Performance: A Systematic Review and Meta-Analysis
Somerville, V., Bringans, C., & Braakhuis, A. J. (2017) · Sports Medicine · doi:10.1007/s40279-017-0675-5 · Cited by 123 · cited 2× · see citing works
“…atom to a free radical [205], whereas polyphenols stimulate stress-related cell signaling pathways and increase the expression of genes encoding proteins, such as nuclear respiratory factor 2 (NRF2), as well as pathways in skeletal muscle, leading to increased mitochondrial biogenesis [206].”
Pedersen, D. J., Lessard, S. J., Coffey, V. G., Churchley, E. G., Wootton, A. M., Ng, T., Watt, M. J., & Hawley, J. A. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01121.2007 · Cited by 122 · cited 3× · see citing works
“Recent evidence suggests caffeine could also positively affect post-exercise recovery owing to its ability to decrease muscle soreness [159] and, when paired with carbohydrates, accelerate muscle glycogen replenishment [160].”
InfluentialEffects of Dietary Fat on Muscle Substrates, Metabolism, and Performance in Athletes
VOGT, M., PUNTSCHART, A., HOWALD, H., MUELLER, B., MANNHART, C., GFELLER-TUESCHER, L., MULLIS, P., & HOPPELER, H. (2003) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000069336.30649.bd · Cited by 120 · cited 1× · see citing works
“However, their availability does not seem to play a role in performance as interventions aimed at increasing IMTG have resulted in either no differences [177] or worsened [178] performance in exercise trials lasting 20–140 min.”
Risk or benefit? Side effects of caffeine supplementation in sport: a systematic review
de Souza, J. G., Coso, J. D., Fonseca, F. D. S., da Silva, B. V. C., de Souza, D. B., Gianoni, R. L. D. S., Filip-Stachnik, A., Serrão, J. C., & Claudino, J. G. (2022) · European Journal of Nutrition · doi:10.1007/s00394-022-02874-3 · Cited by 117 · cited 1× · see citing works
“It is important to note that excessive caffeine intake can lead to adverse effects, including tachycardia, anxiety, headaches, gastrointestinal issues, and a heightened risk of overnight insomnia [172, 173].”
Does Vitamin C and E Supplementation Impair the Favorable Adaptations of Regular Exercise?
Nikolaidis, M. G., Kerksick, C. M., Lamprecht, M., & McAnulty, S. R. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/707941 · Cited by 116 · cited 1× · see citing works
“Vita-mins C and E share a common mechanism of donating a hydrogen atom to a free radical [205], whereas polyphenols stimulate stress-related cell signaling pathways and increase the expression of genes encoding proteins, such as nuclear respiratory factor 2 (NRF2), as well as pathways in skeletal…”
New Horizons in Carbohydrate Research and Application for Endurance Athletes
Podlogar, T., & Wallis, G. A. (2022) · Sports Medicine · doi:10.1007/s40279-022-01757-1 · Cited by 109 · cited 3× · see citing works
“…recovery phase is likely more beneficial than other carbohydrate sources, given its superior efficacy in faster gastrointestinal absorption and glycogen stores and its association with reduced gastrointestinal discomfort when an optimal carbohydrate dosage of 1–1.2 g·kg −1 ⋅ h −1 is consumed [18].”
InfluentialSelf-citationvan Loon, L. J. C., Murphy, R. M., OOSTERLAAR, A. M., Cameron‐Smith, D., Hargreaves, M., Wagenmakers, A. J. M., & Snow, R. J. (2004) · Clinical Science · doi:10.1042/cs20030116 · Cited by 108 · cited 1× · see citing works
“Moreover, Van Loon et al. [151] observed an 18% increase in muscle glycogen content following 5 days of creatine loading (20 g·day –1 ), underscoring a notable glycogen storage boost without significant impacts on fasting plasma insulin levels or GLUT-4 mRNA/protein content.”
Christensen, P. M., Shirai, Y., Ritz, C., & Nordsborg, N. B. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00240 · Cited by 108 · cited 1× · see citing works
“However, even a 1% improvement can be critical in elite sports, potentially making the difference between finishing fourth and securing a podium position in Olympic competitions [88].”
Cunningham, K., & Read, N. W. (1989) · British Journal Of Nutrition · doi:10.1079/bjn19890116 · Cited by 107 · cited 1× · see citing works
“Although consuming dietary fat in the post-exercise meal can prolong gastric emptying times [187], in the context of adequate carbohydrate ingestion, glycogen resynthesis is not influenced by the addition of fat and protein in the 3-h [188] or 24-h [189] post-exercise period.”
Churchward-Venne, T. A., Pinckaers, P. J., Smeets, J. S., Betz, M. W., Senden, J. M., Goessens, J. P., Gijsen, A. P., Rollo, I., Verdijk, L. B., & van Loon, L. J. (2020) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqaa073 · Cited by 106 · cited 1× · see citing works
“…be recommended as it may confer additional benefits, including positive nitrogen balance leading to increased whole-body muscle protein synthesis [93], increased protein content related to mitochondrial biogenesis [94], reduced muscle damage markers [95], and accelerated post-exercise…”
Roy, B. D., & Tarnopolsky, M. A. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.84.3.890 · Cited by 101 · cited 1× · see citing works
“Although consuming dietary fat in the post-exercise meal can prolong gastric emptying times [187], in the context of adequate carbohydrate ingestion, glycogen resynthesis is not influenced by the addition of fat and protein in the 3-h [188] or 24-h [189] post-exercise period.”
Clifford, T., Berntzen, B. J., Davison, G. W., West, D. J., Howatson, G., & Stevenson, E. (2016) · Nutrients · doi:10.3390/nu8080506 · Cited by 101 · cited 2× · see citing works
“Despite reductions in muscle damage and/or inflammation, improvements in performance are not always observed [191, 192].”
Alghannam, A. F., Gonzalez, J. T., & Betts, J. A. (2018) · Nutrients · doi:10.3390/nu10020253 · Cited by 99 · cited 1× · see citing works
“Although carbohydrate intake is the cornerstone of glycogen resynthesis, concomitant intake of protein has been suggested to confer additional benefits, primarily owing to the insulinotropic effects of certain amino acids to reduce muscle protein breakdown [84].”
Supplemental vitamin D enhances the recovery in peak isometric force shortly after intense exercise
Barker, T., Schneider, E. D., Dixon, B. M., et al. (2013) · Nutrition & Metabolism · doi:10.1186/1743-7075-10-69 · Cited by 96 · cited 1× · see citing works
“…[191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence surrounding tart cherry, beetroot, pomegranate, and vitamin D [202, 203].”
Bongiovanni, T., Genovesi, F., Nemmer, M., Carling, C., Alberti, G., & Howatson, G. (2020) · European Journal of Applied Physiology · doi:10.1007/s00421-020-04432-3 · Cited by 96 · cited 1× · see citing works
“…[191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence surrounding tart cherry, beetroot, pomegranate, and vitamin D [202, 203].”
Gonzalez, J. T., Fuchs, C. J., Smith, F. E., Thelwall, P. E., Taylor, R., Stevenson, E. J., Trenell, M. I., Cermak, N. M., & van Loon, L. J. C. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00376.2015 · Cited by 95 · cited 1× · see citing works
“While carbohydrate ingestion during exercise does not substantially affect muscle glycogen utilization [48, 49], it can reduce or even completely suppress liver glycogen breakdown, thereby improving subsequent recovery [49, 50].”
Recovery from prolonged exercise: Restoration of water and electrolyte balance
Maughan, R. J., & Shirreffs, S. M. (1997) · Journal of Sports Sciences · doi:10.1080/026404197367308 · Cited by 92 · cited 1× · see citing works
“Attempts to correct fluid loss induced by exercise should consider the sweat rate, which can vary from 0 to over 2 L·h ⁻ 1 , depending on factors such as environmental conditions, intensity, duration, genetics, fitness level, acclimatization to the environment, and clothing [104, 105].”
Heibel, A. B., Perim, P. H. L., Oliveira, L. F., McNaughton, L. R., & Saunders, B. (2018) · Frontiers in Nutrition · doi:10.3389/fnut.2018.00035 · Cited by 92 · cited 1× · see citing works
“…to rise and is influenced by factors such as the dosage and timing of ingestion [134], supplement form (i.e., solution versus capsules) [123, 135], potential adverse effects, genetic factors related to hydrogen ion (H + ) transporters, the individual’s training status, and exercise type [136].”
Creatine supplementation and endurance performance: surges and sprints to win the race
Forbes, S. C., Candow, D. G., Neto, J. H. F., Kennedy, M. D., Forbes, J. L., Machado, M., Bustillo, E., Gómez-López, J., Zapata, A., & António, J. (2023) · Journal of the International Society of Sports Nutrition · doi:10.1080/15502783.2023.2204071 · Cited by 88 · cited 1× · see citing works
“It is well-documented that creatine supplementation can enhance adaptations to resistance training, including increases in strength, power, and muscular endurance [143].”
Moore, D. R., Areta, J., Coffey, V. G., Stellingwerff, T., Phillips, S. M., Burke, L. M., Cléroux, M., Godin, J.-P., & Hawley, J. A. (2012) · Nutrition & Metabolism · doi:10.1186/1743-7075-9-91 · Cited by 85 · cited 1× · see citing works
“Following the initial protein-based meal after exercise, it is advised that subsequent protein-rich meals follow at 3–4 h intervals [55, 66, 67].”
Naderi, A., de Oliveira, E. P., Ziegenfuss, T. N., & Willems, M. E. T. (2016) · Physical Activity and Nutrition · doi:10.20463/jenb.2016.0031 · Cited by 84 · cited 1× · see citing works
“…threshold depends on the time needed for circulating HCO 3 ⁻ levels to rise and is influenced by factors such as the dosage and timing of ingestion [134], supplement form (i.e., solution versus capsules) [123, 135], potential adverse effects, genetic factors related to hydrogen ion (H + )…”
Self-citationTrommelen, J., van Lieshout, G. A. A., Nyakayiru, J., Holwerda, A. M., Smeets, J. S. J., Hendriks, F. K., van Kranenburg, J. M. X., Zorenc, A. H., Senden, J. M., Goessens, J. P. B., et al. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101324 · Cited by 82 · see citing works
Fructose and Galactose Enhance Postexercise Human Liver Glycogen Synthesis
DÉCOMBAZ, J., JENTJENS, R., ITH, M., SCHEURER, E., BUEHLER, T., JEUKENDRUP, A., & BOESCH, C. (2011) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e318218ca5a · Cited by 80 · cited 2× · see citing works
“Adapted from [13, 21, 24, 27, 28].”
Modulation of glycogen synthesis in rat skeletal muscle by changes in cell volume.
Low, S. Y., Rennie, M. J., & Taylor, P. M. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021594 · Cited by 79 · cited 1× · see citing works
“Furthermore, as an osmotically active compound, creatine can increase intracellular fluid volume [148], which may be beneficial because cell swelling has been identified as a potent stimulus for muscle glycogen synthesis [149].”
Muscle glycogen supercompensation is enhanced by prior creatine supplementation
NELSON, A. G., ARNALL, D. A., KOKKONEN, J., DAY, R., & EVANS, J. (2001) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200107000-00005 · Cited by 79 · cited 1× · see citing works
“In addition, research by Nelson et al. [152] demonstrated that a moderate carbohydrate intake post-creatine loading could enhance muscle glycogen stores by 53% compared with a high-carbohydrate diet alone, further indicating the efficacy of creatine supplementation in enhancing glycogen storage,…”
Stevenson, E., Williams, C., & Nute, M. (2005) · British Journal of Nutrition · doi:10.1079/bjn20051430 · Cited by 78 · cited 1× · see citing works
“…endurance capability following high-GI carbohydrate consumption [39], others found no effect [40–42] or even superior performance with low-GI carbohydrate intake, attributed to improved glucose stability and increased fat oxidation due to lower insulin activity [43] (Supplementary Material 1).”
Glucose Plus Fructose Ingestion for Post-Exercise Recovery—Greater than the Sum of Its Parts?
Gonzalez, J., Fuchs, C., Betts, J., & Van Loon, L. (2017) · Nutrients · doi:10.3390/nu9040344 · Cited by 77 · cited 2× · see citing works
“Therefore, implementing nutritional strategies that reduce liver glycogen utilization during exercise and/or promote its replenishment post-exercise may be as imperative as strategies for muscle glycogen replenishment [8, 47].”
Bonilla, D. A., Pérez-Idárraga, A., Odriozola-Martínez, A., & Kreider, R. B. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18010103 · Cited by 77 · cited 1× · see citing works
“Replenishing glycogen stores through immediate post-exercise carbohydrate intake is crucial for recovery, especially when athletes need to be fully prepared for another training session or competition within 24 h [7–9].”
Trommelen, J., Kouw, I. W. K., Holwerda, A. M., Snijders, T., Halson, S. L., Rollo, I., Verdijk, L. B., & van Loon, L. J. C. (2018) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00273.2016 · Cited by 76 · cited 1× · see citing works
“Considering the extended fasting period during sleep, a pre-sleep protein dose of ≥ 40 g has been recommended to sustain MPS rates and minimize overnight muscle protein breakdown [75, 76].”
Jones, R. L., Stellingwerff, T., Artioli, G. G., Saunders, B., Cooper, S., & Sale, C. (2016) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2015-0286 · Cited by 75 · cited 1× · see citing works
“…3 ⁻ levels to rise and is influenced by factors such as the dosage and timing of ingestion [134], supplement form (i.e., solution versus capsules) [123, 135], potential adverse effects, genetic factors related to hydrogen ion (H + ) transporters, the individual’s training status, and exercise…”
Effect of coingestion of fat and protein with carbohydrate feedings on muscle glycogen storage
Burke, L. M., Collier, G. R., Beasley, S. K., Davis, P. G., Fricker, P. A., Heeley, P., Walder, K., & Hargreaves, M. (1995) · Journal of Applied Physiology · doi:10.1152/jappl.1995.78.6.2187 · Cited by 74 · cited 1× · see citing works
“Although consuming dietary fat in the post-exercise meal can prolong gastric emptying times [187], in the context of adequate carbohydrate ingestion, glycogen resynthesis is not influenced by the addition of fat and protein in the 3-h [188] or 24-h [189] post-exercise period.”
van Loon, L. J. C., Schrauwen-Hinderling, V. B., Koopman, R., Wagenmakers, A. J. M., Hesselink, M. K. C., Schaart, G., Kooi, M. E., & Saris, W. H. M. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00112.2003 · Cited by 74 · cited 1× · see citing works
“Although a low-fat diet can attenuate repletion of IMTG following exercise [180], post-exercise plasma fatty acid availability is increased independently of post-exercise dietary ingestion, mainly due to the hormonal response that stimulates adipose tissue lipolysis and skeletal muscle blood flow…”
Pruscino, C. L., ROSS, M. L. R., Gregory, J. R., Savage, B., & Flanagan, T. (2008) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.18.2.116 · Cited by 73 · cited 2× · see citing works
“Initial studies indicated that NaHCO 3 ingestion before high-intensity exercise attenuated post-exercise blood acid–base imbalance during a 15-min passive recovery period compared with placebo [126] and facilitated a faster restoration of acid–base balance [127].”
Regulation of muscle glycogen repletion, muscle protein synthesis and repair following exercise.
Ivy, J. L. (2004) · Europe PMC (PubMed Central) · Cited by 72 · see citing works
The Importance of Fatty Acids as Nutrients during Post-Exercise Recovery
Lundsgaard, A.-M., Fritzen, A. M., & Kiens, B. (2020) · Nutrients · doi:10.3390/nu12020280 · Cited by 72 · cited 1× · see citing works
“…repletion of IMTG following exercise [180], post-exercise plasma fatty acid availability is increased independently of post-exercise dietary ingestion, mainly due to the hormonal response that stimulates adipose tissue lipolysis and skeletal muscle blood flow during the recovery period [181].”
Chen, H.-Y., Chen, Y., Tung, K., Chao, H.-H., & Wang, H.-S. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01108.2018 · Cited by 68 · cited 1× · see citing works
“Recent evidence suggests caffeine could also positively affect post-exercise recovery owing to its ability to decrease muscle soreness [159] and, when paired with carbohydrates, accelerate muscle glycogen replenishment [160].”
Monteyne, A. J., Coelho, M. O. C., Murton, A. J., Abdelrahman, D. R., Blackwell, J. R., Koscien, C. P., Knapp, K. M., Fulford, J., Finnigan, T. J. A., Dirks, M. L., et al. (2023) · The Journal of Nutrition · doi:10.1016/j.tjnut.2023.02.023 · Cited by 64 · cited 1× · see citing works
“Plant-based proteins such as soy, rice, and pea protein, while effective [82], generally require higher doses (25–40 g) to match the leucine threshold necessary for robust MPS stimulation owing to lower essential amino acid content [53, 74, 83].”
Fructose co‐ingestion to increase carbohydrate availability in athletes
Fuchs, C. J., Gonzalez, J. T., & van Loon, L. J. C. (2019) · The Journal of Physiology · doi:10.1113/jp277116 · Cited by 63 · cited 1× · see citing works
“Therefore, implementing nutritional strategies that reduce liver glycogen utilization during exercise and/or promote its replenishment post-exercise may be as imperative as strategies for muscle glycogen replenishment [8, 47].”
Battram, D. S., Shearer, J., Robinson, D., & Graham, T. E. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00745.2003 · Cited by 61 · cited 2× · see citing works
“However, both studies used carbohydrate doses below the optimal 1.2 g·kg ⁻ 1 ·h ⁻ 1 recommended for maximal glycogen resynthesis [160, 164].”
InfluentialEffects of Dietary Supplements on Adaptations to Endurance Training
Rothschild, J. A., & Bishop, D. J. (2019) · Sports Medicine · doi:10.1007/s40279-019-01185-8 · Cited by 61 · cited 2× · see citing works
“Despite attenuations in markers of metabolic and/or mitochondrial adaptations, no impact on exercise performance outcomes has been observed in human studies when supplementing with vitamins C and/or E during controlled endurance training [210].”
Self-citationRoberts, P. A., Fox, J., Peirce, N., Jones, S. W., Casey, A., & Greenhaff, P. L. (2016) · Amino Acids · doi:10.1007/s00726-016-2252-x · Cited by 59 · cited 1× · see citing works
“Other research has shown that creatine supplementation, combined with a high carbohydrate diet, led to 82% greater glycogen resynthesis within 24 h following exhaustive exercise compared with placebo [150].”
Rustad, P. I., Sailer, M., Cumming, K. T., Jeppesen, P. B., Kolnes, K. J., Sollie, O., Franch, J., Ivy, J. L., Daniel, H., & Jensen, J. (2016) · PLOS ONE · doi:10.1371/journal.pone.0153229 · Cited by 58 · cited 1× · see citing works
“Rustad et al. [89] reported that co-ingesting carbohydrate (0.8 g·kg ⁻ 1 ·h ⁻ 1 ) and protein (0.4 g·kg ⁻ 1 ·h ⁻ 1 ) during the first 2 h of an 18 h of recovery from strenuous cycling exercise led to ~ 14 min longer subsequent exercise capacity compared with carbohydrate intake alone (1.2 g·kg −1…”
InfluentialHutchison, A. T., Flieller, E. B., Dillon, K. J., & Leverett, B. D. (2014) · Journal of Dietary Supplements · doi:10.3109/19390211.2014.952864 · Cited by 56 · cited 1× · see citing works
“…fruit extracts such as tart cherry [191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence surrounding tart cherry, beetroot,…”
Fuchs, C. J., Gonzalez, J. T., Beelen, M., Cermak, N. M., Smith, F. E., Thelwall, P. E., Taylor, R., Trenell, M. I., Stevenson, E. J., & van Loon, L. J. C. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01023.2015 · Cited by 56 · cited 1× · see citing works
“There is currently no evidence to recommend consuming more than 1.2 g·kg −1 ⋅ h −1 of carbohydrates, regardless of type [22, 25].”
InfluentialImpact of muscle glycogen availability on the capacity for repeated exercise in man
ALGHANNAM, A. F., JEDRZEJEWSKI, D., TWEDDLE, M. G., GRIBBLE, H., BILZON, J., THOMPSON, D., TSINTZAS, K., & BETTS, J. A. (2016) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000737 · Cited by 55 · cited 1× · see citing works
“From a performance perspective, several studies have demonstrated that co-ingesting glucose and fructose-based carbohydrates can enhance the recovery of exercise capacity [29–32].”
Intestinal Water Absorption - Implications for the Formulation of Rehydration Solutions
Leiper, J. B. (1998) · International Journal of Sports Medicine · doi:10.1055/s-2007-971977 · Cited by 55 · cited 1× · see citing works
“…as it may confer additional benefits, including positive nitrogen balance leading to increased whole-body muscle protein synthesis [93], increased protein content related to mitochondrial biogenesis [94], reduced muscle damage markers [95], and accelerated post-exercise rehydration [96].”
Bouclin, R., Charbonneau, É., & Renaud, J. (1995) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1995.268.6.c1528 · Cited by 55 · cited 1× · see citing works
“The performance enhancements observed with NaHCO 3 supplementation are attributed to increased extracellular buffering capacity, lowered extracellular potassium (K + ) levels, elevated sodium (Na + ) levels before exercise, and a potential reduction in cellular oxidative stress responses [122–124].”
McCartney, D., Desbrow, B., & Irwin, C. (2017) · Sports Medicine - Open · doi:10.1186/s40798-017-0079-y · Cited by 54 · cited 1× · see citing works
“Therefore, rehydration strategies between exercise bouts recommend that athletes drink fluids equivalent to 125–150% of their body mass lost during exercise [107, 108].”
Whey Protein Improves Marathon-Induced Injury and Exercise Performance in Elite Track Runners
Huang, W.-C., Chang, Y.-C., Chen, Y.-M., Hsu, Y.-J., Huang, C.-C., Kan, N.-W., & Chen, S.-S. (2017) · International Journal of Medical Sciences · doi:10.7150/ijms.19584 · Cited by 54 · cited 1× · see citing works
“…as it may confer additional benefits, including positive nitrogen balance leading to increased whole-body muscle protein synthesis [93], increased protein content related to mitochondrial biogenesis [94], reduced muscle damage markers [95], and accelerated post-exercise rehydration [96].”
McCartney, D., Desbrow, B., & Irwin, C. (2018) · Sports Medicine · doi:10.1007/s40279-017-0800-5 · Cited by 52 · cited 2× · see citing works
“Taken together, combining protein with carbohydrates during recovery periods shorter than 24 h likely has a small, but positive, effect on performance, ranging from 0.6 to 1.6% [87].”
InfluentialPostexercise Muscle Glycogen Synthesis with Combined Glucose and Fructose Ingestion
WALLIS, G. A., HULSTON, C. J., MANN, C. H., ROPER, H. P., TIPTON, K. D., & JEUKENDRUP, A. E. (2008) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31817e0f7e · Cited by 51 · cited 3× · see citing works
“…since glucose and fructose are absorbed via distinct intestinal transporters, it was hypothesized that their combined ingestion could optimize carbohydrate absorption, minimize gastrointestinal discomfort, and potentially maximize muscle glycogen replenishment compared with glucose alone [21].”
InfluentialMartínez-Sánchez, A., Ramos-Campo, D. J., Fernández-Lobato, B., Rubio-Arias, J. A., Alacid, F., & Aguayo, E. (2017) · Food & Nutrition Research · doi:10.1080/16546628.2017.1330098 · Cited by 50 · cited 1× · see citing works
“…be effective in reducing EIMD, including fruit extracts such as tart cherry [191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence…”
Dietary sugars, exercise and hepatic carbohydrate metabolism
Gonzalez, J. T., & Betts, J. A. (2019) · Proceedings of the Nutrition Society · doi:10.1017/s0029665118002604 · Cited by 50 · cited 2× · see citing works
“Research has demonstrated that the rate of liver glycogen resynthesis within the initial 2-h post-exercise period is 30–50% lower than during the subsequent 3–5 h [16].”
Thomson, J. S., Ali, A., & ROWLANDS, D. S. (2011) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h10-104 · Cited by 47 · cited 1× · see citing works
“Nevertheless, it is commonly recommended to rapidly increase amino acid availability following exercise to maximize MPS rates and promote muscle recovery [55, 64], with numerous studies demonstrating positive effects on recovery in endurance athletes [62, 63, 65].”
Gough, L. A., Deb, S. K., Sparks, S. A., & McNaughton, L. R. (2017) · Sports Medicine · doi:10.1007/s40279-017-0699-x · Cited by 46 · cited 1× · see citing works
“…levels to rise and is influenced by factors such as the dosage and timing of ingestion [134], supplement form (i.e., solution versus capsules) [123, 135], potential adverse effects, genetic factors related to hydrogen ion (H + ) transporters, the individual’s training status, and exercise type…”
Hilton, N. P., Leach, N. K., Sparks, S. A., Gough, L. A., Craig, M. M., Deb, S. K., & McNaughton, L. R. (2019) · Sports Medicine - Open · doi:10.1186/s40798-019-0177-0 · Cited by 46 · see citing works
de Oliveira, L. F., Dolan, E., Swinton, P. A., Durkalec-Michalski, K., Artioli, G. G., McNaughton, L. R., & Saunders, B. (2022) · Sports Medicine · doi:10.1007/s40279-021-01575-x · Cited by 46 · cited 2× · see citing works
“This strategy can improve high-intensity exercise performance lasting approximately 30 s to 10 min [121].”
Alternative dietary protein sources to support healthy and active skeletal muscle aging
van der Heijden, I., Monteyne, A. J., Stephens, F. B., & Wall, B. T. (2023) · Nutrition Reviews · doi:10.1093/nutrit/nuac049 · Cited by 45 · cited 1× · see citing works
“Plant-based proteins such as soy, rice, and pea protein, while effective [82], generally require higher doses (25–40 g) to match the leucine threshold necessary for robust MPS stimulation owing to lower essential amino acid content [53, 74, 83].”
Increased Protein Requirements in Female Athletes after Variable-Intensity Exercise
WOODING, D. J., PACKER, J. E., KATO, H., WEST, D. W. D., COURTNEY-MARTIN, G., PENCHARZ, P. B., & MOORE, D. R. (2017) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001366 · Cited by 42 · cited 1× · see citing works
“Endurance athletes are recommended to consume ~ 1.2–1.8 g·kg –1 of high-quality protein [69–72], while those engaged in power-based sports are advised to ingest 1.7–2.2 g·kg –1 [73].”
InfluentialCarbohydrates and Endurance Exercise: A Narrative Review of a Food First Approach
Naderi, A., Gobbi, N., Ali, A., Berjisian, E., Hamidvand, A., Forbes, S. C., Koozehchian, M. S., Karayigit, R., & Saunders, B. (2023) · Nutrients · doi:10.3390/nu15061367 · Cited by 42 · see citing works
Self-citationNutritional Considerations for the Vegan Athlete
West, S., Monteyne, A. J., van der Heijden, I., Stephens, F. B., & Wall, B. T. (2023) · Advances in Nutrition · doi:10.1016/j.advnut.2023.04.012 · Cited by 42 · cited 2× · see citing works
“Plant-based proteins such as soy, rice, and pea protein, while effective [82], generally require higher doses (25–40 g) to match the leucine threshold necessary for robust MPS stimulation owing to lower essential amino acid content [53, 74, 83].”
Wilkinson, K., Koscien, C. P., Monteyne, A. J., Wall, B. T., & Stephens, F. B. (2023) · Physiological Reports · doi:10.14814/phy2.15775 · Cited by 42 · cited 1× · see citing works
“Amounts of essential amino acids, and especially leucine content, in protein sources seem to be the strongest predictor of MPS [79, 80].”
Doering, T. M., Reaburn, P. R., Phillips, S. M., & Jenkins, D. G. (2016) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2015-0102 · Cited by 41 · see citing works
(–)-Epicatechin Supplementation Inhibits Aerobic Adaptations to Cycling Exercise in Humans
Schwarz, N. A., Blahnik, Z. J., Prahad, S. R., McKinley-Barnard, S. K., Holden, S. L., & Waldhelm, A. (2018) · Frontiers in Nutrition · doi:10.3389/fnut.2018.00132 · Cited by 41 · see citing works
Judge, L. W., Bellar, D. M., Popp, J. K., Craig, B. W., Schoeff, M. A., Hoover, D. L., Fox, B. D., Kistler, B. M., & Al‐Nawaiseh, A. M. (2021) · Journal of Human Kinetics · doi:10.2478/hukin-2021-0065 · Cited by 40 · cited 1× · see citing works
“Rehydration is particularly important before subsequent training or competition when limited time is available between exercise bouts in environmentally challenging conditions [101, 102].”
Noakes, T. D. (2022) · Nutrients · doi:10.3390/nu14040862 · Cited by 40 · cited 1× · see citing works
“The liver plays a pivotal role in metabolic regulation during exercise by controlling blood glucose levels through glycogen storage and mobilizing non-carbohydrate sources via gluconeogenesis [26, 46].”
Impact of caffeine and protein on postexercise muscle glycogen synthesis
BEELEN, M., VAN KRANENBURG, J., SENDEN, J. M., KUIPERS, H., & VAN LOON, L. J. C. (2012) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31823a40ef · Cited by 39 · cited 1× · see citing works
“The authors concluded that an optimal carbohydrate dose of 1.2 g·kg ⁻ 1 ·h ⁻ 1 is sufficient to maximize glycogen replenishment rates, with no additional benefits from caffeine co-ingestion [165].”
InfluentialEffects of Differing Dosages of Pomegranate Juice Supplementation after Eccentric Exercise
Machin, D. R., Christmas, K. M., Chou, T., Hill, S. C., Pelt, D. W. V., Trombold, J. R., & Coyle, E. F. (2014) · Physiology Journal · doi:10.1155/2014/271959 · Cited by 39 · cited 1× · see citing works
“Several supplements may be effective in reducing EIMD, including fruit extracts such as tart cherry [191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with…”
Pre-Exercise Alkalosis and Acid-Base Recovery
Siegler, J. C., Keatley, S., Midgley, A. W., Nevill, A. M., & McNaughton, L. R. (2008) · International Journal of Sports Medicine · doi:10.1055/s-2007-989261 · Cited by 39 · cited 1× · see citing works
“Initial studies indicated that NaHCO 3 ingestion before high-intensity exercise attenuated post-exercise blood acid–base imbalance during a 15-min passive recovery period compared with placebo [126] and facilitated a faster restoration of acid–base balance [127].”
Andrade‐Souza, V. A., Bertuzzi, R., de Araújo, G. G., Bishop, D. J., & Lima‐Silva, A. E. (2015) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2014-0268 · Cited by 39 · cited 1× · see citing works
“Conversely, Andrea-Souza et al. [168] did not observe significant performance enhancements in soccer players following co-ingestion of caffeine (6 mg·kg ⁻ 1 ) and carbohydrates (1.2 g·kg ⁻ 1 ·h ⁻ 1 ), possibly owing to insufficient glycogen depletion in the testing protocol.”
InfluentialEffects of Coffee Components on Muscle Glycogen Recovery: A Systematic Review
Loureiro, L. M. R., Reis, C. E. G., & da Costa, T. H. M. (2018) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2017-0342 · Cited by 39 · cited 2× · see citing works
“Loureiro et al. [161] proposed that caffeine might enhance muscle glycogen synthesis by activating molecular pathways related to either energy sensing or muscle contraction.”
Impact of Conjugated Linoleic Acid (CLA) on Skeletal Muscle Metabolism
Kim, Y., Kim, J., Whang, K., & Park, Y. (2016) · Lipids · doi:10.1007/s11745-015-4115-8 · Cited by 38 · cited 1× · see citing works
“Dietary sources include dairy and meat from rumi-nant animals, which are primarily found as the cis -9 trans -11 isomer; however, synthetic isomers have also been studied [185].”
Is Individualization of Sodium Bicarbonate Ingestion Based on Time to Peak Necessary?
de Oliveira, L. F., Saunders, B., Yamaguchi, G. D. C., Swinton, P. A., & Artioli, G. G. (2020) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002313 · Cited by 37 · cited 1× · see citing works
“The lack of performance enhancement in some studies may be due to intraindividual variability in the time required to reach peak HCO ₃ ⁻ levels and the occurrence of gastrointestinal discomfort [127, 132, 133].”
Erith, S., Williams, C., Stevenson, E., Chamberlain, S., Crews, P., & Rushbury, I. (2006) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.16.4.393 · Cited by 36 · cited 1× · see citing works
“…glycemic index, GLu glucose one study found enhanced endurance capability following high-GI carbohydrate consumption [39], others found no effect [40–42] or even superior performance with low-GI carbohydrate intake, attributed to improved glucose stability and increased fat oxidation due to…”
Negaresh, R., Coso, J. D., Mokhtarzade, M., Lima‐Silva, A. E., Baker, J. S., Willems, M. E. T., Talebvand, S., Khodadoost, M., & Farhani, F. (2018) · European Journal of Sport Science · doi:10.1080/17461391.2018.1534990 · Cited by 34 · cited 1× · see citing works
“Moreover, caffeine ingestion alone is sufficient to enhance performance in subsequent sessions for shorter, high-intensity exercises such as wrestling [170] (Supplementary Material 9).”
Fructose Coingestion Does Not Accelerate Postexercise Muscle Glycogen Repletion
TROMMELEN, J., BEELEN, M., PINCKAERS, P. J. M., SENDEN, J. M., CERMAK, N. M., & VAN LOON, L. J. C. (2016) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000829 · Cited by 33 · cited 3× · see citing works
“This finding was confirmed by Trommelen et al. [22], who reported that co-ingesting glucose polymers with fructose or sucrose at a higher dose (1.5 g·kg –1 ⋅ h –1 ) did not further augment muscle glycogen replenishment during a 5-h recovery window, despite a notable reduction in gastrointestinal…”
InfluentialEffects of Creatine and Carbohydrate Loading on Cycling Time Trial Performance
TOMCIK, K. A., CAMERA, D. M., BONE, J. L., ROSS, M. L., JEACOCKE, N. A., TACHTSIS, B., SENDEN, J., VAN LOON, L. J. C., HAWLEY, J. A., & BURKE, L. M. (2018) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001401 · Cited by 33 · cited 1× · see citing works
“However, an individual’s training status may influence creatine’s efficacy regarding glycogen storage, as two studies focusing on highly trained athletes did not show significant enhancements in muscle glycogen levels following creatine supplementation [153, 154].”
Jardine, W. T., Aisbett, B., Kelly, M. K., Burke, L. M., Ross, M. L., Condo, D., Périard, J. D., & Carr, A. J. (2023) · Sports Medicine · doi:10.1007/s40279-023-01885-2 · Cited by 32 · cited 1× · see citing works
“Therefore, rehydration strategies between exercise bouts recommend that athletes drink fluids equivalent to 125–150% of their body mass lost during exercise [107, 108].”
Taylor, C. W., Higham, D., Close, G. L., & Morton, J. P. (2011) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.21.5.410 · Cited by 31 · cited 2× · see citing works
“For instance, Taylor et al. [167] found that caffeine (6 mg·kg –1 ) combined with carbohydrate (1.2 g·kg –1 ·h –1 glucose) improved exercise capacity in an intermittent shuttle run test compared with carbohydrate alone (~ 48 min versus 32 min).”
InfluentialCoingestion of Carbohydrate and Protein on Muscle Glycogen Synthesis after Exercise: A Meta-analysis
MARGOLIS, L. M., ALLEN, J. T., HATCH-MCCHESNEY, A., & PASIAKOS, S. M. (2021) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002476 · Cited by 31 · cited 2× · see citing works
“However, this benefit appears to occur only when protein is added to a suboptimal amount of carbohydrate (e.g., 0.3 g·kg ⁻ 1 ·h ⁻ 1 protein and 0.9 g·kg −1 ⋅ h −1 carbohydrate) [85].”
InfluentialStevenson, E., Williams, C., Nute, M., Humphrey, L., & Witard, O. (2008) · European Journal of Clinical Nutrition · doi:10.1038/sj.ejcn.1602759 · Cited by 30 · see citing works
Van Den Bergh, A. J., Houtman, S., Heerschap, A., Rehrer, N. J., Van Den Boogert, H. J., Oeseburg, B., & Hopman, M. T. E. (1996) · Journal of Applied Physiology · doi:10.1152/jappl.1996.81.4.1495 · Cited by 30 · cited 1× · see citing works
“Early research demonstrated that ingestion of glucose alone increases muscle glycogen levels significantly more than fructose alone [19, 20].”
Postexercise High-Fat Feeding Suppresses p70S6K1 Activity in Human Skeletal Muscle
HAMMOND, K. M., IMPEY, S. G., CURRELL, K., MITCHELL, N., SHEPHERD, S. O., JEROMSON, S., HAWLEY, J. A., CLOSE, G. L., HAMILTON, L. D., SHARPLES, A. P., et al. (2016) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001009 · Cited by 30 · cited 1× · see citing works
“Therefore, athletes can include protein and high-quality fat in the post-exercise window without sacrificing muscle glycogen synthesis, bearing in mind that very high-fat intakes in the post-exercise window may attenuate some, but not all, signaling markers [190].”
Sollie, O., Jeppesen, P. B., Tangen, D. S., Jernerén, F., Nellemann, B., Valsdottir, T. D., Madsen, K., Turner, C., Refsum, H., Skålhegg, B. S., et al. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01132.2017 · Cited by 29 · cited 2× · see citing works
“While the importance of immediate post-exercise protein intake remains debated in literature [59–61], this controversy largely arises from differences in study designs and varying recovery conditions [62, 63].”
Effects of ingesting a sports drink during exercise and recovery on subsequent endurance capacity
LEE, J. K. W., Nio, A. Q. X., Ang, W. H., Law, L. Y. L., & Lim, C. L. (2011) · European Journal of Sport Science · doi:10.1080/17461391.2010.487115 · Cited by 28 · cited 1× · see citing works
“Therefore, water alone may not be the best choice to maximize subsequent exercise capacity [92, 116], especially considering that other nutrients are also essential for recovery.”
Post-exercise muscle glycogen repletion in the extreme: effect of food absence and active recovery.
Fournier, P. A., Fairchild, T. J., Ferreira, L. D., & Bräu, L. (2004) · Europe PMC (PubMed Central) · Cited by 28 · see citing works
Gough, L. A., Brown, D., Deb, S. K., Sparks, S. A., & McNaughton, L. R. (2018) · European Journal of Applied Physiology · doi:10.1007/s00421-018-3975-z · Cited by 28 · cited 1× · see citing works
“In addition, ingesting 0.3 g·kg ⁻ 1 BM of NaHCO ₃ 180 min before exercise led to ~ 3.8% improvement in subsequent performance during four repeats of 2 × 4 km cycling time trials with 40 min passive recovery conducted under hypoxic conditions as compared with placebo [128].”
InfluentialGough, L. A., Deb, S. K., Brown, D., Sparks, S. A., & McNaughton, L. R. (2019) · Journal of Sports Sciences · doi:10.1080/02640414.2019.1568173 · Cited by 28 · cited 1× · see citing works
“In addition, administering NaHCO 3 before exercise can promote acid–base restoration and improve subsequent exercise performance, particularly when the recovery period between sessions is less than 40 min [141].”
Gough, L. A., Rimmer, S., Sparks, S. A., McNaughton, L. R., & Higgins, M. F. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00155 · Cited by 28 · cited 1× · see citing works
“Taken together, administration of NaHCO 3 after exercise can expedite the restoration of acid–base equilibrium following intense physical activity, potentially improving performance during subsequent exercise sessions if an adequate recovery period of 30–90 min is provided [124, 129, 137].”
Dahl, M. A., Areta, J. L., Jeppesen, P. B., Birk, J. B., Johansen, E. I., Ingemann-Hansen, T., Hansen, M., Skålhegg, B. S., Ivy, J. L., Wojtaszewski, J. F. P., et al. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00817.2019 · Cited by 27 · cited 3× · see citing works
“While the importance of immediate post-exercise protein intake remains debated in literature [59–61], this controversy largely arises from differences in study designs and varying recovery conditions [62, 63].”
InfluentialBARZEGAR, H., ARAZI, H., Mohebbi, H., Sheykhlouvand, M., & FORBES, S. C. (2021) · The Journal of Sports Medicine and Physical Fitness · doi:10.23736/s0022-4707.21.12125-5 · Cited by 27 · see citing works
Naderi, A., Rezaei, S., Moussa, A., Levers, K. S., & Earnest, C. P. (2018) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2018.02.013 · Cited by 26 · cited 1× · see citing works
“As an alternative to high-dose antioxidant supplementation, whole fruits and fruit-derived juices or extracts can also provide a good source of antioxidants as well as micronutrients [216].”
Self-citationBandegan, A., Courtney-Martin, G., Rafii, M., Pencharz, P. B., & Lemon, P. W. R. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00174.2018 · Cited by 26 · see citing works
Loureiro, L. M. R., dos Santos Neto, E., Molina, G. E., Amato, A. A., Arruda, S. F., Reis, C. E. G., & da Costa, T. H. M. (2021) · Nutrients · doi:10.3390/nu13103335 · Cited by 26 · cited 1× · see citing works
“Adapted from Gough et al. [129] muscle glycogen resynthesis, finding that the addition of caffeine to milk resulted in approximately 153% higher rates of muscle glycogen synthesis compared with milk alone [166] (Supplementary Material 8).”
Postexercise Fructose–Maltodextrin Ingestion Enhances Subsequent Endurance Capacity
MAUNDER, E., PODLOGAR, T., & WALLIS, G. A. (2018) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001516 · Cited by 25 · cited 1× · see citing works
“For example, Maunder et al. [33] compared the effects of 90 g of maltodextrin mixed with either glucose or fructose (in a 1.5:1 ratio) following a glycogen-depleting run.”
InfluentialSelf-citationFan, P. W., Burns, S. F., & LEE, J. K. W. (2020) · Nutrients · doi:10.3390/nu12123826 · Cited by 24 · cited 1× · see citing works
“However, studies have observed no differences in fluid retention between post-exercise consumption of oral rehydration solutions and sports drinks following exercise-induced dehydration, even in hot conditions [111, 112] or in subsequent endurance performance [113].”
Craven, J., Desbrow, B., Sabapathy, S., Bellinger, P., McCartney, D., & Irwin, C. (2021) · Sports Medicine - Open · doi:10.1186/s40798-020-00297-0 · Cited by 24 · cited 1× · see citing works
“…muscle glycogen stores, reporting that co-ingestion of carbohydrate (0.86 g·kg −1 ⋅ h − 1) with protein (0.27 g·kg −1 ⋅ h −1 ) did not increase muscle glycogen re-synthesis more than carbohydrate per se when ingested at 0.95 g·kg −1 ⋅ h −1 during short-term post-exercise recovery (≤ 8 h) [86].”
InfluentialGough, L. A., & Sparks, S. A. (2024) · Sports Medicine - Open · doi:10.1186/s40798-024-00684-x · Cited by 24 · cited 1× · see citing works
“For athletes with longer recovery periods (> 90 min) who are more susceptible to severe gastrointestinal symptoms, new forms of NaHCO ₃ such as enteric-coated, delayed-release capsules and mini-tablet NaHCO ₃ hydrogels could be considered as they may mitigate gastrointestinal discomfort [138–140].”
Tsao, J.-P., Bernard, J. R., Hsu, H.-C., Hsu, C., Liao, S.-F., & Cheng, I.-S. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.875319 · Cited by 23 · cited 1× · see citing works
“…than subsequent exercise performance, quercetin supplementation for 7 days (1 g ⋅ day −1 ) improved time to exhaustion at 75% maximal oxygen consumption ( V O 2max) by 21.4% following a 3-h recovery period after 60 min of cycling compared with a placebo and also reduced oxidative stress [207].”
InfluentialLópez-Torres, O., Rodríguez-Longobardo, C., Escribano-Tabernero, R., & Fernández-Elías, V. E. (2023) · Nutrients · doi:10.3390/nu15204442 · Cited by 23 · cited 1× · see citing works
“Therefore, re-establishing water and electrolyte balance during the post-exercise recovery period is important [100].”
Tsai, T.-W., Chang, C., Liao, S.-F., Liao, Y., Hou, C., Tsao, J.-P., & Cheng, I.-S. (2017) · British Journal Of Nutrition · doi:10.1017/s0007114517001374 · Cited by 22 · cited 1× · see citing works
“In contrast, 8 weeks of green tea extract supplementation (500 mg ⋅ day −1 ) had no effect on glycogen resynthesis, despite increases in postexercise fat oxidation and exercise-induced muscle GLUT4 protein content [208].”
Morgan, P. T., Wollman, P. M., Jackman, S. R., & Bowtell, J. L. (2018) · Sports · doi:10.3390/sports6040159 · Cited by 21 · cited 1× · see citing works
“…[191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence surrounding tart cherry, beetroot, pomegranate, and vitamin D [202, 203].”
Ly, N., Hamstra-Wright, K. L., & Horswill, C. A. (2023) · Nutrients · doi:10.3390/nu15224759 · Cited by 21 · cited 1× · see citing works
“However, studies have observed no differences in fluid retention between post-exercise consumption of oral rehydration solutions and sports drinks following exercise-induced dehydration, even in hot conditions [111, 112] or in subsequent endurance performance [113].”
Brown, L. J. S., Midgley, A. W., Vince, R. V., Madden, L. A., & McNaughton, L. R. (2013) · Journal of Science and Medicine in Sport · doi:10.1016/j.jsams.2012.10.006 · Cited by 20 · cited 1× · see citing works
“…index, GLu glucose one study found enhanced endurance capability following high-GI carbohydrate consumption [39], others found no effect [40–42] or even superior performance with low-GI carbohydrate intake, attributed to improved glucose stability and increased fat oxidation due to lower…”
Enteric-Coated Sodium Bicarbonate Attenuates Gastrointestinal Side-Effects
Hilton, N. P., Leach, N. K., Craig, M. M., Sparks, S. A., & McNaughton, L. R. (2020) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2019-0151 · Cited by 20 · cited 1× · see citing works
“For athletes with longer recovery periods (> 90 min) who are more susceptible to severe gastrointestinal symptoms, new forms of NaHCO ₃ such as enteric-coated, delayed-release capsules and mini-tablet NaHCO ₃ hydrogels could be considered as they may mitigate gastrointestinal discomfort [138–140].”
The Hyperhydration Potential of Sodium Bicarbonate and Sodium Citrate
Siegler, J. C., Carr, A. J., Jardine, W. T., Convit, L., Cross, R. L., Chapman, D. W., Burke, L. M., & ROSS, M. L. R. (2021) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2021-0179 · Cited by 20 · cited 1× · see citing works
“Another mechanism that may explain the ergogenic effect of post-exercise NaHCO 3 ingestion is its hyperhydration effect, leading to an ~ 8% increase in blood volume through increased sodium availability in the blood [125].”
Comparison of Sports Drink Versus Oral Rehydration Solution During Exercise in the Heat
Schleh, M. W., & Dumke, C. L. (2018) · Wilderness and Environmental Medicine · doi:10.1016/j.wem.2018.01.005 · Cited by 18 · cited 1× · see citing works
“However, studies have observed no differences in fluid retention between post-exercise consumption of oral rehydration solutions and sports drinks following exercise-induced dehydration, even in hot conditions [111, 112] or in subsequent endurance performance [113].”
Tsao, J.-P., Liao, S.-F., Korivi, M., Hou, C.-W., Kuo, C.-H., Wang, H.-F., & Cheng, I.-S. (2015) · Journal of Sports Sciences · doi:10.1080/02640414.2014.970219 · Cited by 17 · cited 2× · see citing works
“…most commonly studied in the context of body composition, humans have also shown an increase in post-exercise muscle GLUT4 protein expression and post-exercise muscle glycogen resynthesis rates following 8 weeks of 3.8 g ⋅ day −1 of trans -10 cis -12 and cis -9 trans -11 CLA supplementation [184].”
InfluentialGough, L. A., Rimmer, S., Osler, C. J., & Higgins, M. F. (2017) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2017-0065 · Cited by 17 · see citing works
McCartney, D., Irwin, C. G., Cox, G. R., & Desbrow, B. (2018) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2018-0176 · Cited by 17 · cited 4× · see citing works
“The mechanism behind this may be related to delayed gastric emptying and increased plasma osmolality, which reduces urine output and enhances fluid retention [117] (Supplementary Material 4, 5).”
InfluentialChapman, S., Chung, H. C., Rawcliffe, A. J., Izard, R., Smith, L., & Roberts, J. D. (2021) · Nutrients · doi:10.3390/nu13051416 · Cited by 17 · cited 1× · see citing works
“Endurance athletes are recommended to consume ~ 1.2–1.8 g·kg –1 of high-quality protein [69–72], while those engaged in power-based sports are advised to ingest 1.7–2.2 g·kg –1 [73].”
InfluentialGurton, W. H., King, D. G., Ranchordas, M. K., Siegler, J. C., & Gough, L. A. (2024) · European Journal of Applied Physiology · doi:10.1007/s00421-024-05578-0 · Cited by 17 · cited 2× · see citing works
“Taken together, administration of NaHCO 3 after exercise can expedite the restoration of acid–base equilibrium following intense physical activity, potentially improving performance during subsequent exercise sessions if an adequate recovery period of 30–90 min is provided [124, 129, 137].”
The Physiological Effects of Creatine Supplementation on Hydration: A Review
Sobolewski, E. J., Thompson, B. J., Smith, A. E., & Ryan, E. D. (2011) · American Journal of Lifestyle Medicine · doi:10.1177/1559827611406071 · Cited by 16 · see citing works
(2019) · Monash University Research Portal (Monash University) · doi:10.5923/j.sports.20190904.01 · Cited by 15 · cited 2× · see citing works
“Milk-based beverages have also led to greater exercise capacity in subsequent exercise performance when compared with both noncaloric and energy-matched beverages, likely due to simultaneously increasing glycogen resynthesis and stimulating muscle protein synthesis [114].”
Gray, E. A., Green, T. A., Betts, J. A., & Gonzalez, J. T. (2020) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2019-0211 · Cited by 15 · cited 1× · see citing works
“Similarly, Gray et al. [34] reported that consuming glucose and fructose during the initial 4 h and again at 15 h of recovery from exhaustive exercise resulted in a notable increase in cycling performance capacity, ~ 27% longer compared with glucose alone.”
Impact of Post-Exercise Fructose-Maltodextrin Ingestion on Subsequent Endurance Performance
Podlogar, T., & Wallis, G. A. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.00082 · Cited by 15 · cited 1× · see citing works
“…trial performance after a glycogen-depleting exercise, participants ingested 1.2 g·kg −1 ·h −1 of a glucose–fructose mix or glucose combined with maltodextrin over a 4-h recovery period before undertaking 1 h of moderate-intensity steady state cycling followed by a ~ 40-min cycling time trial [35].”
InfluentialSelf-citationEffect of Milk on Muscle Glycogen Recovery and Exercise Performance: A Systematic Review
Loureiro, L. M. R., Teixeira, R. D. M., Pereira, I. G. S., Reis, C. E. G., & da Costa, T. H. M. (2020) · Strength and conditioning journal · doi:10.1519/ssc.0000000000000595 · Cited by 14 · cited 1× · see citing works
“…protein kinase (AMPK), possibly through enhanced activation of the Ca 2+ -calmodulin-dependent protein kinase (CaMK) and the phosphorylation of acetyl-CoA carboxylase (ACC), which could collectively induce translocation of GLUT4 to the cell membrane and promote muscle glucose uptake [162, 163].”
López‐Seoane, J., Buitrago-Morales, M., Sáiz, S. L. J., Coso, J. D., & Pareja-Galeano, H. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2128298 · Cited by 14 · cited 1× · see citing works
“Caffeine (1,3,7-trimethylxanthine) is one of the most extensively researched performance-enhancing supplements and is known to enhance exercise performance when consumed before [157] and during prolonged exercise [158].”
Goldstein, E. R., Stout, J. R., Wells, A. J., António, J., Vasenina, E., & Fukuda, D. H. (2023) · Journal of the International Society of Sports Nutrition · doi:10.1080/15502783.2023.2178858 · Cited by 14 · cited 2× · see citing works
“…have reported similar improvements in subsequent time-trial performance and high-intensity interval cycling capacity after either carbohydrates alone or carbohydrate–protein co-ingestion during 2–5 h recovery periods in both young and master endurance athletes [91, 92] (Supplementary Material 3).”
Hansen, M., Oxfeldt, M., Larsen, A. E., Thomsen, L. S., Rokkedal-Lausch, T., Christensen, B., Rittig, N., De Paoli, F. V., Bangsbo, J., Ørtenblad, N., et al. (2020) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-020-00376-3 · Cited by 13 · cited 1× · see citing works
“…as it may confer additional benefits, including positive nitrogen balance leading to increased whole-body muscle protein synthesis [93], increased protein content related to mitochondrial biogenesis [94], reduced muscle damage markers [95], and accelerated post-exercise rehydration [96].”
Ormsbee, M. J., Saracino, P. G., Morrissey, M. C., Donaldson, J., Rentería, L. I., & McKune, A. J. (2022) · Journal of the International Society of Sports Nutrition · doi:10.1080/15502783.2022.2036451 · Cited by 13 · cited 1× · see citing works
“However, two studies investigating this did not observe any positive effects on recovery indices when total daily protein intake is sufficient [77, 78].”
Effect of Glycemic Index Meals on Recovery and Subsequent Endurance Capacity
Wong, S. H., Chen, Y. J., Fung, W. M., & Morris, J. G. (2009) · International Journal of Sports Medicine · doi:10.1055/s-0029-1237710 · Cited by 12 · cited 1× · see citing works
“Fru fructose, Gal galactose, GI glycemic index, GLu glucose one study found enhanced endurance capability following high-GI carbohydrate consumption [39], others found no effect [40–42] or even superior performance with low-GI carbohydrate intake, attributed to improved glucose stability and…”
Borra, V., Brier, N. D., Berry, D. C., Zideman, D. A., Singletary, E. M., Buck, E. D. J. D., & _, _. (2023) · Journal of Athletic Training · doi:10.4085/1062-6050-0682.22 · Cited by 12 · cited 1× · see citing works
“Oral rehydration solutions and sports drinks are common strategies to improve fluid retention owing to their balanced carbohydrate and electrolyte content [110].”
Kim, J., & So, W.-Y. (2019) · Journal of Exercise Science & Fitness · doi:10.1016/j.jesf.2019.01.001 · Cited by 11 · cited 1× · see citing works
“…in reducing EIMD, including fruit extracts such as tart cherry [191], beetroot [192], pomegranate [193], blueberry [194], watermelon [195], grape [196], and blackcurrant [197], as well as vitamin E [198], curcumin [199], cacao [200], and vitamin D [201], with the strongest evidence surrounding…”
Extracellular buffer choice influences acid-base responses and gastrointestinal symptoms
Peacock, J., Sparks, S. A., Middlebrook, I., Hilton, N. P., Tinnion, D. J., Leach, N. K., Saunders, B., & McNaughton, L. R. (2021) · Research in Sports Medicine · doi:10.1080/15438627.2021.1896517 · Cited by 10 · cited 1× · see citing works
“The lack of performance enhancement in some studies may be due to intraindividual variability in the time required to reach peak HCO ₃ ⁻ levels and the occurrence of gastrointestinal discomfort [127, 132, 133].”
Gurton, W. H., Macrae, H. Z., Gough, L. A., & King, D. G. (2021) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2020-1120 · Cited by 10 · cited 1× · see citing works
“3), while others have reported that a shorter recovery time of 35 min may be inadequate to restored acid–base balance to improve subsequent exercise capacity [131] (Supplementary Material 6).”
Díaz‐Lara, J., Reisman, E., Botella, J., Probert, B., Burke, L. M., Bishop, D. J., & Lee, M. J. (2024) · Acta Physiologica · doi:10.1111/apha.14215 · Cited by 10 · cited 1× · see citing works
“In contrast, delaying post-exercise carbohydrate ingestion by 2 h can lead to reduced muscle glycogen concentrations 4 h after exercise compared with immediate ingestion [13] and may impair exercise performance the following day [14].”
Flagged first, then by citations
2 of the 218 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- Jeukendrup AE, Gleeson M. Sport nutrition. 4th ed. Champaign: Human Kinetics; 2025.
- Gough LA, et al. Post-exercise supplementation of sodium bicarbonate improves acid base balance recovery and subsequent high-intensity boxing specific performance. Front Nutr. 2019;6:155. · DOI · Paper page
Cited by
Sorted by citations
Goals in Nutrition Science 2025–2030
Berry, E. M., Cardoso, B. R. L., Cash, S. B., Cifuentes, A., Collado, M. C., le Coutre, J., German, J. B., Ibáñez, E., Lawrence, M. A., Nieman, D. C., et al. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1784021 · Cited by 7 · see citing works
“Sport and exercise nutrition is focused on the optimization of dietary strategies to support and enhance training adaptations, performance, health, and metabolic recovery (155–157).”
Dou, Y., Wang, Y., Zhang, W., Jiang, Y., Zhang, J., Yang, T., Han, Z., Li, Y., Liu, C., & Ren, D. (2026) · Nutrients · doi:10.3390/nu18050724 · Cited by 5 · see citing works
“…maximal output, recent research has increasingly shifted attention toward the role of nutritional supplementation in supporting metabolic efficiency, recovery processes, and performance maintenance during repeated high-intensity loading, particularly when recovery windows are limited [2].”
Triathlon: Ergo Nutrition for Training, Competing, and Recovering
Miguel‐Ortega, Á., Rodríguez-Rodrigo, M.-A., Mielgo‐Ayuso, J., & Calleja-González, J. (2025) · Nutrients · doi:10.3390/nu17111846 · Cited by 4 · see citing works
“Studies show that consuming 7–12 g of CHO per kilogram of body weight in the 1–3 days before the competition can significantly improve performance in prolonged tests [95].”
Stalmans, M., Narang, B. J., Vermaerke, N., Engelbrecht, L., Lauriks, W., Robberechts, R., Ramaekers, M., Koppo, K., Debevec, T., & Poffé, C. (2026) · The Journal of Physiology · doi:10.1113/jp290041 · Cited by 5 · see citing works
Exploring the Gut Microbiome in Combat Sports: A Systematic Scoping Review
Carlone, J., Rossi, C., Bianco, A., Drid, P., Parisi, A., & Fasano, A. (2026) · Sports · doi:10.3390/sports14010019 · Cited by 2 · see citing works
“Incorporating dietary variables as covariates allows for a clearer understanding of the relative influence of training and competitive stress versus diet [82].”
Sasikumar, R., Gupta, A., Selva Kumar, T., Kaviarasu, G., Haorongbam, S., Rajarathinam, R., Janghu, S., Panda, S. K., & Jaiswal, A. K. (2026) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.70775 · Cited by 2 · see citing works
A U-shaped dose–response of carbohydrate–protein supplementation on rowing performance
Wang, X., & Wu, H. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1651457 · Cited by 2 · see citing works
Medium-chain fatty acids activate fructose metabolism via up-regulating GLUT5-KHK axis
Hou, J., Li, J., Zhao, C., Yin, S., & Hu, H. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.153358 · Cited by 1 · see citing works
Synergistic effects of creatine, carbs, protein on repeated sprint performance
Wang, Y., Wei, H., Cheng, X., & Chen, Z. (2026) · Scientific Reports · doi:10.1038/s41598-026-44278-x · Cited by 1 · see citing works
Crisafulli, O., Fortunati, M., Brindisi, F., Nuredini, A., Palermi, S., Tupler, R. G., Voet, N. B. M., Odone, A., & D’Antona, G. (2026) · European Journal of Applied Physiology · doi:10.1007/s00421-026-06338-y · Cited by 1 · see citing works
“It is well established that both aerobic and anaerobic training adaptations can be enhanced through the synergistic effects of appropriate nutritional strategies and/or supplementation (Deng et al. 2025; Naderi et al. 2025).”
Caffeine and human performance: from molecular mechanisms to exercise and recovery
Leng, J., Yu, J. K., Li, Z. L., Zhang, Y., & Cui, J. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2026.1871149 · Cited by 2 · see citing works
Qamar, M., & Khan, M. Z. (2025) · Premier Journal of Sports Science · doi:10.70389/pjsps.100009
Altarriba-Bartés, A., Peña, J., Puig-Povill, M., Bau, J. C., Calleja-González, J., & Vicens‐Bordas, J. (2025) · International Journal of Sports Science & Coaching · doi:10.1177/17479541251390501
Post-Exercise Nutrition Knowledge and Adherence to Recommendations Among Amateur Endurance Athletes
Csanaky, L., Asztalos, Á. C., Tóth, D., Polyák, É., & Figler, M. (2025) · Nutrients · doi:10.3390/nu17223629 · Cited by 1 · see citing works
“Consuming adequate carbohydrates in this critical period is essential for athletes engaging in frequent and intensive endurance training, as it enables proper recovery before the next training session [13,14,17].”
Cahyono, D., Indardi, N., Huda, M. S., et al. (2025) · Research Square · doi:10.21203/rs.3.rs-7917627/v1
Kim, J. Y., Kim, S. Y., Lee, S. M., & An, Y. H. (2025) · Physical Activity and Nutrition · doi:10.20463/pan.2025.0038
“These factors directly contribute to improved performance 3 .”
SLEEP OPTIMIZATION FOR RECOVERY, HEALTH AND PERFORMANCE IN ATHLETES - A LITERATURE REVIEW
Bernecka, P., Sójkowska-Sławińska, O., Leśniewska, A., Macuk, P., Gniedziejko, M., Roszak, J., Skorupski, B. M., Strumnik, N., & Firkowska, A. (2025) · International Journal of Innovative Technologies in Social Science · doi:10.31435/ijitss.4(48).2025.4426
A influência de micronutrientes na recuperação de jogadores de futebol: Revisão narrativa
Rodrigues, W. C. C., Junior, A. M. A. F., Paraguassu, L. T. V., et al. (2026) · Research Society and Development · doi:10.33448/rsd-v15i1.50514
Micronutrients in Sports Supplements: Biochemical Functions and Health Impacts
Jadeja, H., Patel, M., & Patel, B. M. (2026) · Advances in biochemistry in health and disease · doi:10.1007/978-3-032-14441-6_1
Kosendiak, A. A., Konieczko, D., & Biernat, E. (2026) · Nutrients · doi:10.3390/nu18060887
“Inversely, adequate nutrition and supplementation help limit injuries, inflammation, and post-exercise pain [7,8].”
Plant-derived exosome-like vesicles enhance exercise-induced muscle recovery and sleep quality
Aykora, E., & Aykora, D. (2026) · Nutrition Research · doi:10.1016/j.nutres.2026.03.005
Advances in Sport Physiology, Nutrition, and Metabolism
Bojarczuk, A. (2026) · Applied Sciences · doi:10.3390/app16063061
“Consequently, research in sport and exercise science aims to understand physiological responses to exercise [7], metabolic adaptations to training [8], and the role of nutritional strategies in supporting performance and recovery in physically active and athletic populations [9].”
Dietary Fiber in Sport: Implications for Performance and Body Composition Optimization
Özduran, E., & Karadağ, M. G. (2026) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2025-0170
Stelzer, T. C., Kripp, A. M., Draxler, A., Maqboul, L., Pfeiffer, K. T., Bulmer, A. C., König, D., & Wagner, K.-H. (2026) · Sports Medicine - Open · doi:10.1186/s40798-026-01011-2
“However, this only becomes relevant at exercise durations of 90 min and more [31].”
Yaghoobi, E., Pashaei, F., Allsopp, G. L., Retallack, M., Charalambous, N., Snipe, R. M. J., Shaw, C. S., Kowalski, G. M., Bruce, C. R., Hunter, A. M., et al. (2026) · Nutrients · doi:10.3390/nu18091447 · Cited by 1 · see citing works
Kamkaen, N., Tanantong, T., Siri, P., et al. (2026) · IGI Global eBooks · doi:10.4018/979-8-3373-9544-9.ch002
Villanova, S., Gatti, M., Colosio, M., et al. (2026) · Nutrients · doi:10.3390/nu18101598
“Recent studies have indicated that certain dietary interventions, such as a carbohydrate-rich diet, can help prevent the onset of OTS and facilitate recovery [11].”
Mardiana, Oksidriyani, S., Rokhmah, F. D., et al. (2026) · Sport Sciences for Health · doi:10.1007/s11332-026-01811-9
“This observation indicates that carbohydrate source may play a more important role during the early stages of recovery, whereas longer-term adaptations may be influenced by broader physiological processes related to training stimulus and metabolic regulation [3].”
InfluentialNassif, C., Cannon, J., & Marino, F. E. (2026) · European Journal of Applied Physiology · doi:10.1007/s00421-026-06368-6 · Cited by 1 · see citing works
“Recent work has renewed attention on the post-exercise period, where CHO intake is recommended to accelerate glycogen restoration and support capacity for subsequent endurance exercise (Gonzalez and Wallis 2021; Naderi et al. 2025 ).”
dos Santos, J. A. R., Zacca, R., Fernandes, D. G., Oliveira, P. S., & Carvalho, D. (2026) · Sports · doi:10.3390/sports14080325
“Variations in training volume [7], intensity [8], and frequency [9], alongside recovery strategies [10] and nutritional status [11], modulate the direction and magnitude of these adaptations.”
Książek, A. (2026) · Nutrients · doi:10.3390/nu18152552
“Because effective recovery may facilitate subsequent exercise performance and support long-term training adaptations, nutritional and supplementation interventions are receiving increasing attention as potential strategies to support post-exercise recovery [12].”
Żmuda, A. R., Kudłacik, A., Łukasik, J., Franków, M., Jarosz, K. A., Schmidt, A. K., Całusińska-Skowron, M., Jeziorowska, K., Bałdys, K., & Kaczmarek, O. (2026) · International Journal of Innovative Technologies in Social Science · doi:10.31435/ijitss.3(51).2026.6511
Song, K.-T., Lee, H., Sung, J., Baek, J.-K., Park, S.-W., Hyun, K.-J., Jin, E.-H., Noh, K.-W., & Park, S. (2026) · Nutrients · doi:10.3390/nu18172855
“Pertaining to CHO availability, contemporary reviews have highlighted that protein co-ingestion appears most ergogenic when total CHO intake is moderate, rather than maximized, and when exercise duration or frequency imposes repeated stress within a single day or a short microcycle [46,47].”
Lee, E.-J., & Kim, J. (2026) · Applied Sciences · doi:10.3390/app16178713
Integrative Nutritional Strategies for Performance, Recovery, and Weight Management in Taekwondo
Amawi, A. T., Alkasasbeh, W. J., Grivas, G. V., Jalali, P., & Mohammadi, A. (2026) · Nutrients · doi:10.3390/nu18172894
“High-intensity combat efforts may result in glycogen depletion, neuromuscular fatigue, muscle damage, and fluid loss, making the timing and practical implementation of recovery strategies particularly important when subsequent bouts or training sessions follow within a short period [8,78].”
Dairy-derived nutrition across the lifespan: digestion, bioavailability, and healthy aging
Hasegawa, Y., Adams, J. A., Weaver, S., & Ozturk, G. (2026) · International Journal of Food Properties · doi:10.1080/10942912.2026.2722805
Nieman, D. C., Sakaguchi, C. A., & Scalli, A. C. A. M. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-40334-7.00041-1
Hadi, E. M. A. A., Ouali, E. M. E., Akhittouch, A., Rimy, H., Zehhaf, F., Kassimi, K., Chokri, A., Zahi, B., Elgot, A., & Barkaoui, M. (2026) · Journal of the International Society of Sports Nutrition · doi:10.1080/15502783.2026.2730213
“In this context, dietary intake and energy availability play a central role in supporting muscle regeneration, glycogen resynthesis and overall recovery processes [11].”
Suruji, A., Alkhaldy, A. A., Alghafari, W. T., & Qahwaji, D. M. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1940147
Zhang, J., Li, Y., Wei, B., Li, X., Xiao, Z., Wu, X., Ye, X., & Zhang, S. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2026.1960237
“This is particularly important for athletes facing short recovery intervals or repeated competition demands (Bongiovanni et al., 2020; Naderi et al., 2025).”
Nguyen, D. H. N., Yu, T.-W., Quach, Q. B., Raja, A., Chen, C., Kuo, M. J., Truong, T. N., & Li, S. (2026) · Nutrients · doi:10.3390/nu18183049
“Post-exercise recovery is a central component of sports nutrition because it influences subsequent training quality, performance readiness, and long-term adaptation [1,2].”
Enhancing Recovery in Soccer: A Scoping Review on Nutritional and Supplementation Strategies
Martinho, D. V., Clemente, F. M., Sarmento, H., Costa, J. A., Oliveira, M. V., Field, A., Rebelo, A., Nunes, N. A., Kaľata, M., Zahálka, F., et al. (2026) · International Journal of Sports Physiology and Performance · doi:10.1123/ijspp.2025-0634
Nutrition, Hydration, and Recovery: Optimizing Performance
Ketterly, J., Mandel, C., Hueglin, S., Baker, L., Lozano, J. M. O., Murray, T., King, K., Nguyen, D., Mack, R., & Wittstein, J. R. (2026) · Operative Techniques in Sports Medicine · doi:10.1016/j.otsm.2026.151289
- Authors
- Naderi, A., Rothschild, J. A., Santos, H. O., Hamidvand, A., Koozehchian, M. S., Ghazzagh, A., Berjisian, E., & Podlogar, T.
- Affiliations
- Islamic Azad University Boroujerd Branch (IR)
- Auckland University of Technology (NZ)
- Shahid Beheshti University (IR)
- Jacksonville State University (US)
- Tarbiat Modares University (IR)
- Edith Cowan University (AU)
- University of Exeter (GB)
- Corresponding author
- Naderi, Alireza
- Podlogar, Tim
- ORCID
- Venue
- Sports Medicine
- Published
- 2025-04-12
- Volume
- 55
- Issue
- 7
- Pages
- 1559-1577
- ISSN
- 0112-1642 (ISSN-L)
- 1179-2035
- PMC
- PMC12297025
- OpenAlex
- W4409384105
- Cited by
- 43
- References
- 218
- Citations by year
- 2026: 36 · 2025: 8
- FWCI
- 7.22
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Sports Medicine (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion, cc-by)
- Australasian Journal of Paramedicine (submittedVersion, cc-by)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Sports Performance and Training
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Keywords
- post-exercise recovery, exercise performance, carbohydrate intake, glycogen resynthesis, protein intake, muscle damage, creatine, caffeine
- MeSH terms
- Post-Exercise Recovery, Antioxidants, Caffeine, Creatine, Dietary Carbohydrates, Dietary Proteins, Glycogen
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-08.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-08.
Cited sources are checked by gpt-6-sol.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review