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Isolating the effects of carbohydrate and lipid availability on exercise-induced skeletal muscle signalling in males

  • Universidad de Castilla-La Mancha
  • Chulabhorn Royal Academy
  • Ghent University
  • University of Nottingham

Research output: Contribution to journalArticlepeer-review

3   Link opens in a new tab Citations (SciVal)

Abstract

Abstract: Training with low carbohydrate availability can increase AMP-activated protein kinase (AMPK) activation, but whether increased AMPK activation is the result of low carbohydrate availability per se or concurrent increases in fatty acid availability/oxidation is unclear. This study assessed the independent effects of carbohydrate and fatty acid availability on exercise-induced skeletal muscle AMPK activation and downstream signalling. Eight active males who were aged between 18 and 60 years with a body mass index in the range 18.0–30.0 kg m −2 cycled on three occasions for 60 min at 95% of lactate threshold 1 with ingestion of either carbohydrate (CARB), niacin (NIACIN) or placebo (FAST) in a crossover design (11 ± 6 days washout). Blood and exhaled breath were sampled throughout exercise and muscle was sampled pre- and post-exercise. Fat oxidation and plasma non-esterified fatty acid concentrations were both lower in CARB vs. FAST with negligible difference between CARB vs. NIACIN. Plasma insulin concentrations were higher in CARB compared with both FAST and NIACIN. Net muscle glycogen use was greater with NIACIN vs. CARB. Although no evidence for differences were observed for phosphorylated AMPK, the downstream target, phosphorylated acetyl-CoA carboxylase was decreased with CARB vs. both FAST (–0.7 ± 0.6 fold, P = 0.04) and NIACIN (–1.0 ± 0.8 fold, P = 0.02). RNA-sequencing displayed several canonical changes with exercise but little difference between conditions. These data suggest carbohydrate ingestion suppresses exercise-induced phosphorylation of acetyl-CoA carboxylase independent of fatty acid availability. (Figure presented.). Key points: It is currently unknown whether the enhanced physiological adaptation to regularly exercising in a fasted-state are explained by low carbohydrate availability and/or the concomitant increase in fatty acid availability. This study used fasted exercise with niacin ingestion to reduce the lipaemic response associated with fasted exercise to isolate the effects of carbohydrate vs. fatty acid availability on exercise-induced skeletal muscle signalling. Our data show niacin ingestion increases muscle glycogen utilisation compared to carbohydrate ingestion during exercise, but both niacin and carbohydrate ingestion suppress fatty acid availability and fat oxidation to a similar extent. Our data demonstrate carbohydrate ingestion during exercise suppresses acetyl-CoA carboxylase phosphorylation compared to both niacin ingestion and extended overnight fasting. These data suggest that high carbohydrate availability inhibits exercise-induced acetyl-CoA carboxylase phosphorylation in human skeletal muscle, independent of circulating fatty acid concentrations.

Original languageEnglish
Pages (from-to)267-281
Number of pages15
JournalJournal of Physiology
Volume604
Issue number1
Early online date16 Nov 2025
DOIs
Publication statusPublished - 1 Jan 2026

Data Availability Statement

Data for this study are openly available at reasearchdata.bath.ac.uk and https://www.ncbi.nlm.nih.gov/geo.

Funding

JTG has received research funding from BBSRC, MRC, British Heart Foundation, Clasado Biosciences, Lucozade Ribena Suntory, ARLA Foods Ingredients, Cosun Nutrition Center and the Fruit Juice Science Centre; is a scientific advisory board member to ZOE; and has completed paid consultancy for 6d Sports Nutrition, The Dairy Council, PepsiCo, Violicom Medical, Tour Racing Ltd and SVGC. For a full list of disclosures see https://sites.google.com/view/declarationsgonzalez/home . JAB is an investigator on research grants funded by BBSRC, MRC, NIHR, British Heart Foundation, Rare Disease Foundation, EU Hydration Institute, GlaxoSmithKline, Nestlé, Lucozade Ribena Suntory, ARLA foods, Cosun Nutrition Center, American Academy of Sleep Medicine Foundation, Salus Optima (L3M Technologies Ltd) and the Restricted Growth Association; has completed paid consultancy for PepsiCo, Kellogg's, SVGC and Salus Optima (L3M Technologies Ltd); is an Advisor to StudySetGo Ltd; is Company Director of Metabolic Solutions Ltd; receives an annual honorarium as a member of the academic advisory board for the International Olympic Committee Diploma in Sports Nutrition; and receives an annual stipend as Editor‐in Chief of International Journal of Sport Nutrition & Exercise Metabolism. This study was funded by The University of Bath.

Funders
Rare Disease Foundation
International Olympic Committee Diploma in Sports Nutrition
Fruit Juice Science Centre
American Academy of Sleep Medicine Foundation
Medical Research Council
SVGC
Salus Optima
Biotechnology and Biological Sciences Research Council
Dairy Council
National Institute for Health and Care Research
Clasado Biosciences
British Heart Foundation
PepsiCo
L3M Technologies Ltd
Cosun Nutrition Center
University of Bath
GlaxoSmithKline
Restricted Growth Association
ARLA Foods Ingredients
EU Hydration Institute

Keywords

  • carbohydrate metabolism
  • cell signalling
  • exercise metabolism
  • lipid metabolism

ASJC Scopus subject areas

  • Physiology

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