Skeletal muscle metabolism is highly dependent on mitochondrial function, with impaired mitochondrial biogenesis associated with the development of metabolic diseases such as insulin resistance and type 2 diabetes. Mitochondria display substantial plasticity in skeletal muscle, and are highly sensitive to levels of physical activity. It is thought that physical activity promotes mitochondrial biogenesis in skeletal muscle through increased expression of genes encoded in both the nuclear and the mitochondrial genome; however, how this process is co-ordinated at the cellular level is poorly understood. Nuclear receptors (NRs) are key signalling proteins capable of integrating environmental factors and mitochondrial function, thereby providing a potential link between exercise and mitochondrial biogenesis. The aim of this review is to highlight the function of NRs in skeletal muscle mitochondrial biogenesis and discuss the therapeutic potential of NRs for the management and treatment of chronic metabolic disease.
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Review Article|
July 14 2015
Regulation of skeletal muscle mitochondrial function by nuclear receptors: implications for health and disease
Joaquin Perez-Schindler;
Joaquin Perez-Schindler
*MRC-ARUK Centre for Musculoskeletal Ageing Research, School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, UK
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Andrew Philp
*MRC-ARUK Centre for Musculoskeletal Ageing Research, School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, UK
Correspondence: Andrew Philp (email: [email protected]).
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Publisher: Portland Press Ltd
Received:
April 01 2015
Revision Received:
May 12 2015
Accepted:
May 26 2015
Online ISSN: 1470-8736
Print ISSN: 0143-5221
© 2015 Authors; published by Portland Press Limited
2015
Clin Sci (Lond) (2015) 129 (7): 589–599.
Article history
Received:
April 01 2015
Revision Received:
May 12 2015
Accepted:
May 26 2015
Citation
Joaquin Perez-Schindler, Andrew Philp; Regulation of skeletal muscle mitochondrial function by nuclear receptors: implications for health and disease. Clin Sci (Lond) 1 October 2015; 129 (7): 589–599. doi: https://doi.org/10.1042/CS20150246
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