Diurnal variation in skeletal muscle mitochondrial function dictates time‐of‐day‐dependent exercise capacity

Exercise impinges on almost all physiological processes at an organismal level and is a potent intervention to treat various diseases. Exercise performance is well established to display diurnal rhythm, peaking during the late active phase. However, the underlying molecular/metabolic factors and mitochondrial energetics that possibly dictate time-of-day exercise capacity remain unknown. Here, we have unraveled the importance of diurnal variation in mitochondrial functions as a determinant of skeletal muscle exercise performance. Our results show that exercise-induced muscle metabolome and mitochondrial energetics are distinct at ZT3 and ZT15. Importantly, we have elucidated key diurnal differences in mitochondrial functions that are well correlated with disparate time-of-day-dependent exercise capacity. Providing causal mechanistic evidence, we illustrate that loss of Sirtuin4 (SIRT4), a well-known mitochondrial regulator, abrogates mitochondrial diurnal variation and consequently abolishes time-of-day-dependent muscle output. Therefore, our findings unequivocally demonstrate the pivotal role of baseline skeletal muscle mitochondrial functions in dictating diurnal exercise capacity.

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Publication Details

Journal
The FASEB Journal
Published
2025-02-04
DOI
https://doi.org/10.1096/fj.202402930r
Citations
1
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
1.16

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article

Diurnal variation in skeletal muscle mitochondrial function dictates time‐of‐day‐dependent exercise capacity

Subhash Khatri, Ullas Kolthur‐Seetharam, Sunil Laxman, Mohit Kashiv et al.
1 citations
The FASEB Journal
Adipose Tissue and Metabolism
1.16
article

Diurnal variation in skeletal muscle mitochondrial function dictates time‐of‐day‐dependent exercise capacity

Subhash Khatri, Ullas Kolthur‐Seetharam, Sunil Laxman, Mohit Kashiv, Anshit Singh, Souparno Das, Md. Faiz Ahmad
article en
1 citations

Abstract

Exercise impinges on almost all physiological processes at an organismal level and is a potent intervention to treat various diseases. Exercise performance is well established to display diurnal rhythm, peaking during the late active phase. However, the underlying molecular/metabolic factors and mitochondrial energetics that possibly dictate time-of-day exercise capacity remain unknown. Here, we have unraveled the importance of diurnal variation in mitochondrial functions as a determinant of skeletal muscle exercise performance. Our results show that exercise-induced muscle metabolome and mitochondrial energetics are distinct at ZT3 and ZT15. Importantly, we have elucidated key diurnal differences in mitochondrial functions that are well correlated with disparate time-of-day-dependent exercise capacity. Providing causal mechanistic evidence, we illustrate that loss of Sirtuin4 (SIRT4), a well-known mitochondrial regulator, abrogates mitochondrial diurnal variation and consequently abolishes time-of-day-dependent muscle output. Therefore, our findings unequivocally demonstrate the pivotal role of baseline skeletal muscle mitochondrial functions in dictating diurnal exercise capacity.

The FASEB JournalVol. 39(3)
Tata Institute of Fundamental Research (IN), Institute for Stem Cell Biology and Regenerative Medicine (IN), Centre for DNA Fingerprinting and Diagnostics (IN)
Wellcome Trust, National Institute of Mental Health and Neurosciences, Tata Institute of Fundamental Research, Department of Biotechnology, Ministry of Science and Technology, India, Department of Science and Technology, Ministry of Science and Technology, India, Department of Atomic Energy, Government of India, Indian Institute of Science Education and Research Pune, The Wellcome Trust DBT India Alliance, Indian Institute of Science Education and Research Mohali, National Centre for Biological Sciences, Advanced Centre for Treatment, Research and Education in Cancer
Good health and well-being
Openalex Percentile: Top 26%
Adipose Tissue and Metabolism
1.16
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