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Role of Age-Related Mitochondrial Dysfunction in Sarcopenia

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2020 Jul 29
PMID 32718064
Citations 66
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Abstract

Skeletal muscle aging is associated with a significant loss of skeletal muscle strength and power (i.e., dynapenia), muscle mass and quality of life, a phenomenon known as sarcopenia. This condition affects nearly one-third of the older population and is one of the main factors leading to negative health outcomes in geriatric patients. Notwithstanding the exact mechanisms responsible for sarcopenia are not fully understood, mitochondria have emerged as one of the central regulators of sarcopenia. In fact, there is a wide consensus on the assumption that the loss of mitochondrial integrity in myocytes is the main factor leading to muscle degeneration. Mitochondria are also key players in senescence. It has been largely proven that the modulation of mitochondrial functions can induce the death of senescent cells and that removal of senescent cells improves musculoskeletal health, quality, and function. In this review, the crosstalk among mitochondria, cellular senescence, and sarcopenia will be discussed with the aim to elucidate the role that the musculoskeletal cellular senescence may play in the onset of sarcopenia through the mediation of mitochondria.

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References
1.
Egan B, Zierath J . Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell Metab. 2013; 17(2):162-84. DOI: 10.1016/j.cmet.2012.12.012. View

2.
Janssen I, Heymsfield S, Wang Z, Ross R . Skeletal muscle mass and distribution in 468 men and women aged 18-88 yr. J Appl Physiol (1985). 2000; 89(1):81-8. DOI: 10.1152/jappl.2000.89.1.81. View

3.
Frontera W, Ochala J . Skeletal muscle: a brief review of structure and function. Calcif Tissue Int. 2014; 96(3):183-95. DOI: 10.1007/s00223-014-9915-y. View

4.
Clark B, Manini T . Sarcopenia =/= dynapenia. J Gerontol A Biol Sci Med Sci. 2008; 63(8):829-34. DOI: 10.1093/gerona/63.8.829. View

5.
Franzini-Armstrong C, Boncompagni S . The evolution of the mitochondria-to-calcium release units relationship in vertebrate skeletal muscles. J Biomed Biotechnol. 2011; 2011:830573. PMC: 3196067. DOI: 10.1155/2011/830573. View