The DOI matches its Crossref record; 216 of the 218 references it cites were found in a registry or an index; 43 of the 83 sources its claims cite were checked for support.
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.
Overview
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
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Cites
Statistics
Figures

![Fig. 2 Influence of timing (a) and type (b–d), of carbohydrate (CHO) on glycogen resynthesis *indicates significant differenes (p < 0.05) from other groups within a given study. Adapted from [13, 21, 24, 27, 28]. Fru fructose, Gal galactose, GI glycemic index, GLu glucose](/paper-figures/4fff1246573949109aaf82f13792a8cc/nutritional-strategies-to-improve-post-exercise-recovery-and-subsequent-exercise-figure-2.jpg)
![Fig. 3 Sodium bicarbonate (NaHCO3) ingested 30 min following exercise to exhaustion can increase pH (a) and improve time to exhaustion during a subsequent exercise bout (b). Recovery period is highlighted in a. *Denotes significant differences between groups (p < 0.05). Adapted from Gough et al. [129]](/paper-figures/1d87f71c262c43018e2bd62afb045966/nutritional-strategies-to-improve-post-exercise-recovery-and-subsequent-exercise-figure-3.jpg)
Verification
Claims the paper makes
21 Partly supported · 18 No full text of the sources · 5 Supported · 4 Own interpretation · 2 Supported so far · 1 Not supported · 1 Couldn’t confirm · accuracy not yet measured
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“There is currently no evidence to recommend consuming more than 1.2 g·kg−1⋅h−1 of carbohydrates, regardless of type [22, 25].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Not checked — no full text of the sourcecites [22] Trommelen J, et al. Fructose coingestion does not accelerate postexercise muscle glycogen repletion. Med Sci Sports Exerc. 2016;48(5):907–12. source
- Disputedcites [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. sourceExperimental — accuracy not yet measured
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.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Supportedcites [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
Section 3.2, “Refuel” (page unavailable), recommends a high-carbohydrate meal within two hours of exercise when rapid recovery is needed. It specifically emphasizes glycogen replenishment for athletes training twice in one day or competing on consecutive days, consistent with the claim’s short turnaround. (LLM, conf=0.89)
- Supportedcites [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
The Introduction says glycogen repletion is especially important when optimal performance must be regained within 24 hours, including during intensive training and multiday competitions. The Conclusions and recommendations advise starting carbohydrate intake as soon as possible after exercise when rapid recovery and maximal performance within 24 hours are needed. (LLM, conf=0.94)
- Not matchedcites [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.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Partly supportedcites [15] Burke LM, et al. Carbohydrates for training and competition. J Sports Sci. 2011;29(Suppl 1):S17-27. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [16] Gonzalez JT, Betts JA. Dietary sugars, exercise and hepatic carbohydrate metabolism. Proc Nutr Soc. 2019;78(2):246–56. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [17] Murray B, Rosenbloom C. Fundamentals of glycogen metabolism for coaches and athletes. Nutr Rev. 2018;76(4):243–59. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [18] Podlogar T, Wallis GA. New horizons in carbohydrate research and application for endurance athletes. Sports Med. 2022;52(Suppl 1):5–23. sourceExperimental — accuracy not yet measured
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)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“and may impair exercise performance the following day [14]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Partly supportedcites [16] Gonzalez JT, Betts JA. Dietary sugars, exercise and hepatic carbohydrate metabolism. Proc Nutr Soc. 2019;78(2):246–56. sourceExperimental — accuracy not yet measured
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)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Protein
What the sources say
- Not checked — no full text of the sourcecites [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
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“However, the influence of GI on subsequent exercise performance appears inconsistent.”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Not checked — no full text of the sourcecites [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
- Not checked — no full text of the sourcecites [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
- Not checked — no full text of the sourcecites [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
- Not checked — no full text of the sourcecites [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
- Could not verifycites [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. sourceExperimental — accuracy not yet measured
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)
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Carbohydrate and Protein Co-ingestion
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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.”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“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]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Carbohydrate and Protein Co-ingestion
What the sources say
- Supportedcites [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
The Abstract Results report the same mean carbohydrate and protein intake rates and find no improvement in muscle glycogen re-synthesis with carbohydrate plus protein versus carbohydrate alone. The Conclusion places this finding in short-term post-exercise recovery (≤8 h). Page numbers are not provided in our copy. (LLM, conf=0.94)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
- Probably not a substantial claim. 3
- It may state two separate claims as one. 13
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“while those engaged in power-based sports are advised to ingest 1.7–2.2 g·kg–1 [73]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Protein
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“a pre-sleep protein dose of ≥ 40 g has been recommended to sustain MPS rates and minimize overnight muscle protein breakdown [75, 76]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Protein
What the sources say
- Not checked — no full text of the sourcecites [75] Res PT, et al. Protein ingestion before sleep improves postexercise overnight recovery. Med Sci Sports Exerc. 2012;44(8):1560–9. source
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Partly supportedcites [18] Podlogar T, Wallis GA. New horizons in carbohydrate research and application for endurance athletes. Sports Med. 2022;52(Suppl 1):5–23. sourceExperimental — accuracy not yet measured
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Endurance athletes are recommended to consume ~ 1.2–1.8 g·kg–1 of high-quality protein [69–72]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Protein
What the sources say
- Not checked — no full text of the sourcecites [69] Tarnopolsky M. Protein requirements for endurance athletes. Nutrition. 2004;20(7–8):662–8. source
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
- Not checked — no full text of the sourcecites [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
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
Every source the paper cites for this claim was checked and supports it.
In the paper
“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]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Supportedcites [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
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Protein
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“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]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Supportedcites [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 During Competition section says gastrointestinal issues are less prevalent when fructose is co-ingested with glucose and recommends glucose–fructose mixtures. The Post-Competition section reports quicker liver glycogen replenishment with these mixtures than with glucose-based carbohydrates alone. Page numbers are unavailable in our copy. (LLM, conf=0.92)
- Not checked — no full text of the sourcecites [22] Trommelen J, et al. Fructose coingestion does not accelerate postexercise muscle glycogen repletion. Med Sci Sports Exerc. 2016;48(5):907–12. source
- Not checked — no full text of the sourcecites [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
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
hedgedconditional- Asserted: passes — The authors put it forward as true.
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Carbohydrate and Protein Co-ingestion
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
- Supportedcites [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
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
hedgedconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Fluid and Electrolytes
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedgeddirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“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]”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade II—Moderate Evidence > Sodium Bicarbonate
What the sources say
- Not checked — no full text of the sourcecites [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
- Supportedcites [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
The Experimental Design and Protocol section reports NaHCO3 ingestion 10 minutes into a 75-minute recovery period. The Discussion reports that acid–base measures recovered and subsequent boxing performance improved; it also describes a prior study using ingestion 30 minutes into a 90-minute recovery period that improved subsequent cycling capacity. The supplied passages have no page numbers. (LLM, conf=0.93)
hedgedconditional- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Exercising in a dehydrated state is well-established to negatively affect both performance and health [97, 98].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Fluid and Electrolytes
What the sources say
- Partly supportedcites [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. sourceExperimental — accuracy not yet measured
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)
- Partly supportedcites [98] Maughan RJ, Shirreffs SM. Dehydration and rehydration in competative sport. Scand J Med Sci Sports. 2010;20(Suppl 3):40–7. sourceExperimental — accuracy not yet measured
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)
boosteddirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
- Partly supported
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“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].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Protein
What the sources say
- Not checked — no full text of the sourcecites [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
- Not checked — no full text of the sourcecites [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
- Not checked — no full text of the sourcecites [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
- Not checked — no full text of the sourcecites [54] Tipton KD, Wolfe RR. Protein and amino acids for athletes. J Sports Sci. 2004;22(1):65–79. source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“Effective post-exercise recovery is critical for restoring physiological homeostasis, repairing muscle damage, replenishing energy stores, and facilitating adaptations that enhance athletic performance [1].”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Introduction
What the sources say
- Not checked — no full text of the sourcecites [1] Kenttä G, Hassmén P. Overtraining and recovery. A conceptual model. Sports Med. 1998;26(1):1–16. source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“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”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
What the sources say
- Not checked — no full text of the sourcecites [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
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“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”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Dietary Carbohydrates
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
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.
Rated major: it would touch a result — a value a result rests on, reported and recomputed p-values on opposite sides of the significance level, two passages that conflict with no sign which is right, or a cited work retracted before this paper was published.
In the paper
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Conclusions
“Replacement of 150–200% of lost sweat within 4–8 h is advised for effective rehydration”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Fluid and Electrolytes
“rehydration strategies between exercise bouts recommend that athletes drink fluids equivalent to 125–150% of their body mass lost during exercise [107, 108].”
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Conclusions
“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”
§ Nutritional Strategies to Improve Post-exercise Recovery and Subsequent Exercise Performance: A Narrative Review > Grade I—Strong Evidence > Protein
“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].”
Citations
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×
“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×
“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×
“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×
“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×
“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×
“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
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×
“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×
“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×
“…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
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×
“…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×
“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 695
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×
“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×
“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×
“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×
“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×
“…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×
“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].”
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 357 · cited 1×
“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].”
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×
“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 318 · cited 1×
“…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].”
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×
“…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 291 · cited 1×
“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×
“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×
“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×
“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×
“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×
“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×
“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×
“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., & Sebastianelli, W. J. (1998) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199801000-00010 · Cited by 234 · cited 1×
“…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×
“…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×
“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
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×
“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].”
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 216 · cited 1×
“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].”
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×
“These benefits are likely due to antioxidant effects and have been observed in both trained and untrained populations [203].”
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×
“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×
“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
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×
“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×
“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
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×
“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×
“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×
“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×
“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×
“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].”
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 171 · cited 1×
“…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…”
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 168 · cited 1×
“…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].”
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 168 · cited 1×
“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×
“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×
“Exercising in a dehydrated state is well-established to negatively affect both performance and health [97, 98].”
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×
“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×
“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×
“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×
“…[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×
“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×
“In addition, creatine supplementation may positively affect muscle glycogen storage in the days following glycogen-depleting exercise [144].”
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 149
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×
“…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
Burke, L. M. (2017) · Sports Medicine · doi:10.1007/s40279-017-0687-1 · Cited by 141
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×
“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×
“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×
“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×
“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].”
InfluentialSwifter, higher, stronger: What’s on the menu?
Burke, L. M., & Hawley, J. A. (2018) · Science · doi:10.1126/science.aau2093 · Cited by 135 · cited 1×
“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].”
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×
“…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×
“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].”
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 129 · cited 2×
“…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].”
Kato, H., Suzuki, K., Bannai, M., & Moore, D. R. (2016) · PLOS ONE · doi:10.1371/journal.pone.0157406 · Cited by 128
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 124 · cited 1×
“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].”
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×
“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×
“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.”
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×
“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…”
van 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 113 · cited 1×
“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 113 · cited 1×
“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].”
Alghannam, A. F., Gonzalez, J. T., & Betts, J. A. (2018) · Nutrients · doi:10.3390/nu10020253 · Cited by 109 · cited 1×
“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].”
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×
“…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-citationCunningham, K., & Read, N. W. (1989) · British Journal Of Nutrition · doi:10.1079/bjn19890116 · Cited by 107 · cited 1×
“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×
“…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 103 · cited 1×
“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×
“Despite reductions in muscle damage and/or inflammation, improvements in performance are not always observed [191, 192].”
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 101 · cited 1×
“…[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].”
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 97 · cited 1×
“It is well-documented that creatine supplementation can enhance adaptations to resistance training, including increases in strength, power, and muscular endurance [143].”
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×
“…[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×
“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×
“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×
“…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].”
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 89 · cited 1×
“…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-citationMoore, 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×
“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].”
Trommelen, 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
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×
“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×
“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×
“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×
“…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×
“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×
“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×
“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×
“…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×
“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×
“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×
“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
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×
“…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].”
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 71 · cited 1×
“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].”
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×
“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].”
Effects 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 64 · cited 2×
“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-citationMonteyne, 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×
“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].”
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×
“However, both studies used carbohydrate doses below the optimal 1.2 g·kg ⁻ 1 ·h ⁻ 1 recommended for maximal glycogen resynthesis [160, 164].”
InfluentialRoberts, 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×
“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×
“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×
“…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×
“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×
“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×
“…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×
“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×
“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×
“…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×
“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×
“…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×
“…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×
“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×
“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×
“…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
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×
“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×
“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 44 · cited 1×
“Amounts of essential amino acids, and especially leucine content, in protein sources seem to be the strongest predictor of MPS [79, 80].”
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×
“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
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×
“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].”
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
(–)-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
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×
“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×
“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×
“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×
“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×
“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×
“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.”
InfluentialImpact 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 39 · cited 1×
“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].”
Effects 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×
“Loureiro et al. [161] proposed that caffeine might enhance muscle glycogen synthesis by activating molecular pathways related to either energy sensing or muscle contraction.”
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×
“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×
“…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×
“Moreover, caffeine ingestion alone is sufficient to enhance performance in subsequent sessions for shorter, high-intensity exercises such as wrestling [170] (Supplementary Material 9).”
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 33 · cited 2×
“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).”
InfluentialFructose 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×
“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×
“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×
“Therefore, rehydration strategies between exercise bouts recommend that athletes drink fluids equivalent to 125–150% of their body mass lost during exercise [107, 108].”
Coingestion 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×
“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
Muscle glycogen recovery after exercise during glucose and fructose intake monitored by13C-NMR
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×
“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×
“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×
“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×
“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
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×
“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×
“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×
“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 28 · cited 3×
“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].”
InfluentialTsao, 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 27 · cited 1×
“…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].”
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
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×
“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
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×
“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×
“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×
“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×
“…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×
“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].”
López-Torres, O., Rodríguez-Longobardo, C., Escribano-Tabernero, R., & Fernández-Elías, V. E. (2023) · Nutrients · doi:10.3390/nu15204442 · Cited by 23 · cited 1×
“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×
“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×
“…[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×
“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×
“…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×
“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×
“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].”
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 19 · cited 1×
“…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-citationComparison 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×
“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].”
Gurton, 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 18 · cited 2×
“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].”
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×
“…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
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×
“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×
“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].”
InfluentialThe 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
(2019) · Monash University Research Portal (Monash University) · doi:10.5923/j.sports.20190904.01 · Cited by 15 · cited 2×
“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×
“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.”
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 15 · cited 1×
“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 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×
“…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×
“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×
“…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×
“…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].”
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×
“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…”
Valenzuela, P. L., Alejo, L. B., Montalvo‐Pérez, A., Ojanguren, D., Górriz, M., Aldazabal, I. P., Ozcoidi, L. M., Lucía, A., & Barranco‐Gil, D. (2023) · Journal of the International Society of Sports Nutrition · doi:10.1080/15502783.2023.2166366 · Cited by 12 · cited 1×
“However, two studies investigating this did not observe any positive effects on recovery indices when total daily protein intake is sufficient [77, 78].”
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×
“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×
“…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×
“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×
“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).”
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 8
“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
“…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 5
“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
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
“Incorporating dietary variables as covariates allows for a clearer understanding of the relative influence of training and competitive stress versus diet [82].”
Metadata
- 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
- 77
- References
- 218
- Citations by year
- 2026: 62 · 2025: 15
- FWCI
- 8.14
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Sports Medicine (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Australasian Journal of Paramedicine (submittedVersion, cc-by)
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Sports Performance and Training
- Health Sciences › Medicine › Physiology (medical) › Exercise and Physiological Responses
- Keywords
- post-exercise recovery, exercise performance, carbohydrate intake, glycogen resynthesis, protein intake, muscle damage, creatine, caffeine, hydration, electrolyte solutions, milk beverages, omega-3 fatty acids, antioxidants, sodium bicarbonate, acid-base balance, micronutrients, athletes
- MeSH terms
- Post-Exercise Recovery, Antioxidants, Caffeine, Creatine, Dietary Carbohydrates, Dietary Proteins, Glycogen, Humans, Exercise, Fatty Acids, Omega-3, Muscle, Skeletal, Micronutrients, Dietary Supplements, Athletic Performance, Sports Nutritional Physiological Phenomena
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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 ›
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