Cited by 50Muscle metabolism and nutritionExercise and Physiological ResponsesCardiovascular and exercise physiology

Sodium bicarbonate ingestion augments the increase in PGC-1α mRNA expression during recovery from intense interval exercise in human skeletal muscle

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Percival, Michael E., Martin, Brian J., Gillen, Jenna B., Skelly, Lauren E., MacInnis, Martin J., Green, Alex E., Tarnopolsky, Mark A., Gibala, Martin J.·2015·Journal of Applied Physiology

Abstract

We tested the hypothesis that ingestion of sodium bicarbonate (NaHCO 3) prior to an acute session of high-intensity interval training (HIIT) would augment signaling cascades and gene expression linked to mitochondrial biogenesis in human skeletal muscle. On two occasions separated by ∼1 wk, nine men (mean ± SD: age 22 ± 2 yr, weight 78 ± 13 kg, V̇o 2 peak 48 ± 8 ml·kg−1·min−1) performed 10 × 60-s cycling efforts at an intensity eliciting ∼90% of maximal heart rate (263 ± 40 W), interspersed with 60 s of recovery. In a double-blind, crossover manner, subjects ingested a total of 0.4 g/kg body weight NaHCO 3 before exercise (BICARB) or an equimolar amount of a placebo, sodium chloride (PLAC). Venous blood bicarbonate and pH were elevated at all time points after ingestion ( P < 0.05) in BICARB vs. PLAC. During exercise, muscle glycogen utilization (126 ± 47 vs. 53 ± 38 mmol/kg dry weight, P < 0.05) and blood lactate accumulation (12.8 ± 2.6 vs. 10.5 ± 2.8 mmol/liter, P < 0.05) were greater in BICARB vs. PLAC. The acute exercise-induced increase in the phosphorylation of acetyl-CoA carboxylase, a downstream marker of AMP-activated protein kinase activity, and p38 mitogen-activated protein kinase were similar between treatments ( P > 0.05). However, the increase in PGC-1α mRNA expression after 3 h of recovery was higher in BICARB vs. PLAC (approximately sevenfold vs. fivefold compared with rest, P < 0.05). We conclude that NaHCO 3 before HIIT alters the mRNA expression of this key regulatory protein associated with mitochondrial biogenesis. The elevated PGC-1α mRNA response provides a putative mechanism to explain the enhanced mitochondrial adaptation observed after chronic HIIT supplemented with NaHCO 3 in rats.

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Crossref · 10.1152/japplphysiol.00048.2015

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  • Sodium bicarbonate supplementation resulted in significantly higher levels of PGC-1-α, a key protein known to drive mitochondrial adaptations.

    “Interestingly, Percival and investigators [499] reported that sodium bicarbonate supplementation resulted in significantly higher levels of PGC-1-α, a key protein known to drive mitochondrial adaptations.”

    From ISSN exercise &amp; sports nutrition review update: research &amp; recommendations (2018) · cites this paper as [499]

    The Muscle Data section reports a significantly greater increase in PGC-1α mRNA after bicarbonate supplementation, but says the nuclear abundance of PGC-1α protein was not different at any point. The citing sentence describes higher levels of the protein, which is contrary to the reported protein result. (LLM, conf=0.86)

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  • Sodium bicarbonate promotes non-oxidative energy metabolism, as observed through greater muscle lactate production and muscle glycogen utilization during intermittent exercise performed in the severe-intensity domain.

    “Evidence suggests that sodium bicarbonate promotes non-oxidative energy metabolism, as observed through greater muscle lactate production and muscle glycogen utilization during intermittent exercise performed in the severe-intensity domain (Percival et al., 2015).”

    From Acute enteric-coated sodium bicarbonate has negligible effect on anaerobic performance but affects metabolomics and attenuates the gastrointestinal response (2022) · cites this paper as Percival et al., 2015

    The Abstract reports greater muscle glycogen utilization and blood lactate accumulation with sodium bicarbonate during high-intensity interval cycling. The Blood and Muscle Metabolites section (page not supplied) explicitly says muscle lactate was not measured in this study, so the claimed observation of greater muscle lactate production is not supported. (LLM, conf=0.88)

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Authors
Percival, M. E., Martin, B. J., Gillen, J. B., Skelly, L. E., MacInnis, M. J., Green, A. E., Tarnopolsky, M. A., & Gibala, M. J.
Affiliations
McMaster University (CA)
Corresponding author
Gibala, Martin J.
Venue
Journal of Applied Physiology
Published
2015-12-01
Volume
119
Issue
11
Pages
1303-1312
ISSN
  • 0161-7567 (ISSN-L)
  • 8750-7587
  • 1522-1601
OpenAlex
W797190648
Cited by
50
References
71
Citations by year
2026: 2 · 2025: 2 · 2024: 4 · 2023: 4 · 2022: 7 · 2021: 2 · 2020: 6 · 2019: 8 · 2018: 6 · 2017: 4 · 2016: 5
FWCI
2.67
Type
journal article
Language
en
Open access
Locations
  • Journal of Applied Physiology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • MacSphere (McMaster University) (submittedVersion)
  • MacSphere (McMaster University)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
  • Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
  • Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
Keywords
sodium bicarbonate ingestion, PGC-1α, mitochondrial biogenesis, high-intensity interval training, skeletal muscle, post-exercise recovery, muscle glycogen utilization, blood lactate, AMPK, p38 MAPK, bicarbonate buffering, exercise adaptation
MeSH terms
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Adult, Bicarbonates, Double-Blind Method, Glycogen, Heart Rate, Humans, Male, Mitochondria, Muscle, Phosphorylation, RNA, Messenger, Transcription Factors, Exercise, Sodium Bicarbonate, Muscle, Skeletal, Cross-Over Studies, p38 Mitogen-Activated Protein Kinases, Young Adult

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