The DOI matches its Crossref record; 350 of the 350 references it cites were found in a registry or an index.
Exercise metabolism and adaptation in skeletal muscle
Open accessAbstract
Viewing metabolism through the lens of exercise biology has proven an accessible and practical strategy to gain new insights into local and systemic metabolic regulation. Recent methodological developments have advanced understanding of the central role of skeletal muscle in many exercise-associated health benefits and have uncovered the molecular underpinnings driving adaptive responses to training regimens. In this Review, we provide a contemporary view of the metabolic flexibility and functional plasticity of skeletal muscle in response to exercise. First, we provide background on the macrostructure and ultrastructure of skeletal muscle fibres, highlighting the current understanding of sarcomeric networks and mitochondrial subpopulations. Next, we discuss acute exercise skeletal muscle metabolism and the signalling, transcriptional and epigenetic regulation of adaptations to exercise training. We address knowledge gaps throughout and propose future directions for the field. This Review contextualizes recent research of skeletal muscle exercise metabolism, framing further advances and translation into practice.
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“Aging is accompanied by a progressive decline in physiological resilience, often manifesting as impaired metabolic flexibility, reduced skeletal muscle function, chronic low-grade inflammation, and increased susceptibility to sarcopenia, frailty, and cardiometabolic diseases [1].”
From Exercise-Induced Muscle–Fat Crosstalk: Molecular Mediators and Their Pharmacological Modulation for the Maintenance of Metabolic Flexibility in Aging (2025) · cites this paper as [1]
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Skeletal muscle mass and distribution in 468 men and women aged 18–88 yr
Janssen, I., Heymsfield, S. B., Wang, Z., & Ross, R. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.1.81 · Cited by 3,087
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
Lin, J., Wu, H., Tarr, P. T., Zhang, C.-Y., Wu, Z., Boss, O., Michael, L. F., Puigserver, P., Isotani, E., Olson, E. N., et al. (2002) · Nature · doi:10.1038/nature00904 · Cited by 2,546
AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1α
Jäger, S., Handschin, C., St.-Pierre, J., & Spiegelman, B. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705070104 · Cited by 2,491
D’Hulst, G., Soro-Arnaiz, I., Masschelein, E., Veys, K., Fitzgerald, G., Smeuninx, B., Kim, S., Deldicque, L., Blaauw, B., Carmeliet, P., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-13889-6 · Cited by 2,310
What is the cause of the ageing atrophy?
Lexell, J. E., Taylor, C. C., & Sjöstróm, M. (1988) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(88)90132-3 · Cited by 2,142
A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporter
Stefani, D. D., Raffaello, A., Teardo, E., Szabó, I., & Rizzuto, R. (2011) · Nature · doi:10.1038/nature10230 · Cited by 1,957
Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter
Baughman, J. M., Perocchi, F., Girgis, H. S., Plovanich, M., Belcher-Timme, C. A., Sancak, Y., Bao, X. R., Strittmatter, L., Goldberger, O., Bogorad, R. L., et al. (2011) · Nature · doi:10.1038/nature10234 · Cited by 1,953
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
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
Cogliati, S., Frezza, C., Soriano, M. E., Varanita, T., Quintana-Cabrera, R., Corrado, M., Cipolat, S., Costa, V., Casarin, A., Gomes, L. C., et al. (2013) · Cell · doi:10.1016/j.cell.2013.08.032 · Cited by 1,265
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Kurhaluk, N., & Tkaczenko, H. (2025) · Nutrients · doi:10.3390/nu17040665 · Cited by 62
Myokines: Metabolic regulation in obesity and type 2 diabetes
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“Aging is accompanied by a progressive decline in physiological resilience, often manifesting as impaired metabolic flexibility, reduced skeletal muscle function, chronic low-grade inflammation, and increased susceptibility to sarcopenia, frailty, and cardiometabolic diseases [1].”
Identification of Genomic Predictors of Muscle Fiber Size
Guilherme, J. P. L. F., Semenova, E. A., Kikuchi, N., Homma, H., Kozuma, A., Saito, M., Zempo, H., Matsumoto, S., Kobatake, N., Nakazato, K., et al. (2024) · Cells · doi:10.3390/cells13141212 · Cited by 11
Xu, M., & Liu, X. (2026) · Biomolecules · doi:10.3390/biom16030406 · Cited by 6
Metadata
- Authors
- Smith, J. A. B., Murach, K. A., Dyar, K. A., & Zierath, J. R.
- Affiliations
- Karolinska Institutet (SE)
- University of Arkansas at Fayetteville (US)
- Helmholtz Munich (DE)
- University of Copenhagen (DK)
- Corresponding author
- Zierath, Juleen R.
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2023-05-24
- Volume
- 24
- Issue
- 9
- Pages
- 607-632
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC10527431
- OpenAlex
- W4377989871
- Cited by
- 342
- References
- 350
- Citations by year
- 2026: 138 · 2025: 113 · 2024: 74 · 2023: 17
- FWCI
- 9.02
- Type
- journal article
- Language
- en
- Open access
- Licence
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (publishedVersion, other-oa)
- PubMed Central (acceptedVersion)
- PuSH - Publication Server of Helmholtz Zentrum München (submittedVersion)
- Funders
- Novo Nordisk (NNF18CC0034900)
- Vetenskapsrådet (2015-00165)
- Centrum för idrottsforskning (P2022-0013, P2023-0093)
- Novo Nordisk Fonden (NNF 18 CC0034900, NNF22OC0077741)
- Novo Nordisk Foundation Center for Basic Metabolic Research (NNF 18 CC0034900)
- National Institutes of Health (AG063994)
- National Institute on Aging (R00AG063994)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Physiology (medical) › Cardiovascular and exercise physiology
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Keywords
- skeletal muscle metabolism, exercise adaptation, metabolic flexibility, muscle fiber ultrastructure, sarcomere, mitochondrial subpopulations, acute exercise, exercise training, epigenetic regulation, transcriptional regulation, signaling pathways, muscle plasticity
- MeSH terms
- Adaptation, Physiological, Mitochondria, Exercise, Muscle, Skeletal, Epigenesis, Genetic
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