Impact of exercise and fasting on mitochondrial regulators in human muscle
Author:
Menezes Eveline S.1, Islam Hashim2, Arhen Benjamin B.1, Simpson Craig A.1, McGlory Chris1, Gurd Brendon J.1
Affiliation:
1. School of Kinesiology and Health Studies , Queen’s University , Kingston , ON , Canada 2. School of Health and Exercise Sciences , University of British Columbia – Okanagan , Kelowna , BC , Canada
Abstract
Abstract
Objectives
To investigate the impact of acute energetic stress (acute HIIE and fasting) on ERRγ, PPARβ, NR1D1, NR4A1, and TFEB in human skeletal muscle.
Methods
The current study performed secondary analyses using muscle biopsy samples from two previously published studies: study 1) leg muscle biopsies from nine men and eight women were obtained pre and 3 h following acute high-intensity interval cycling exercise (HIIE); study 2) leg muscle biopsies were obtained from nine men pre-, during, and post-an 8 h fast with or without 2 h of arm ergometer exercise. RT-PCR was performed on samples from each study to determine the mRNA expression of ERRγ, PPARβ, NR1D1, NR4A1, and TFEB. Additionally, we retrieved data from meta-analyzed human muscle gene expression using the publicly available database MetaMex.
Results
PGC-1α (p<0.01, d=1.98) and NR4A1 (p<0.01, d=1.36) mRNA expression significantly increased while TFEB (p≤0.05, d=0.70) decreased following HIIE. Significant decreases in NR4A1 and NR1D1 mRNA expression were observed following an 8 h fast. Our MetaMex analyses revealed significant increases (p<0.05) in PGC-1α and NR4A1 expression following aerobic and resistance exercise, and in PPARβ expression following resistance exercise.
Conclusions
Our data indicate that acute HIIE stimulates increases in NR4A1 and PGC-1α and decreases in TFEB mRNA expression in human skeletal muscle. Additionally, a short term (8 h) fast reduced the mRNA expression of the transcriptional regulators NR4A1 and NR1D1 – potentially as a mechanism of decreasing mitochondrial biogenesis to reduce energy expenditure during a period of restricted energy availability.
Funder
Natural Sciences and Engineering Research Council of Canada
Publisher
Walter de Gruyter GmbH
Reference52 articles.
1. Bishop, DJ, Hawley, JA. Reassessing the relationship between mRNA levels and protein abundance in exercised skeletal muscles. Nat Rev Mol Cell Biol 2022. https://doi.org/10.1038/s41580-022-00541-3. 2. Leick, L, Wojtaszewski, JF, Johansen, ST, Kiilerich, K, Comes, G, Hellsten, Y, et al.. PGC-1alpha is not mandatory for exercise- and training-induced adaptive gene responses in mouse skeletal muscle. Am J Physiol Endocrinol Metab 2008;294:E463–74. https://doi.org/10.1152/ajpendo.00666.2007. 3. Kuhnen, G, Guedes Russomanno, T, Murgia, M, Pillon, NJ, Schönfelder, M, Wackerhage, H. Genes whose gain or loss of function changes type 1, 2A, 2X, or 2B muscle fibre proportions in mice – a systematic review. Int J Mol Sci 2022;23. https://doi.org/10.3390/ijms232112933. 4. Islam, H, Hood, DA, Gurd, BJ. Looking beyond PGC-1α: emerging regulators of exercise-induced skeletal muscle mitochondrial biogenesis and their activation by dietary compounds. Appl Physiol, Nutr, Metab 2020;45:11–23. https://doi.org/10.1139/apnm-2019-0069. 5. Rovina, RL, da Rocha, AL, Marafon, BB, Pauli, JR, de Moura, LP, Cintra, DE, et al.. One bout of aerobic exercise can enhance the expression of Nr1d1 in oxidative skeletal muscle samples. Front Physiol 2021;12. https://doi.org/10.3389/fphys.2021.626096.
|
|