Age-associated Mitochondrial Dysfunction in Skeletal Muscle: Contributing Factors and Suggestions for Long-term Interventions

被引:53
作者
Huang, Julianna H. [1 ]
Hood, David A. [1 ,2 ]
机构
[1] York Univ, Sch Kinesiol & Hlth Sci, N York, ON M3J 1P3, Canada
[2] York Univ, Muscle Hlth Res Ctr, Toronto, ON M3J 2R7, Canada
关键词
ageing; biogenesis; exercise; mitochondria; oxidative stress; reactive oxygen species; DNA-DELETION MUTATIONS; CYTOCHROME-C-OXIDASE; LIFELONG CALORIE RESTRICTION; ANTIOXIDANT ENZYME-ACTIVITY; OXIDATIVE STRESS; PROTEIN IMPORT; TRANSCRIPTION FACTOR; GENE-EXPRESSION; CONTRACTILE ACTIVITY; H2O2; RELEASE;
D O I
10.1002/iub.164
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been established that the impairment of mitochondrial function is associated with various disorders, such as type 2 diabetes and Alzheimer's disease. In addition, mitochondria have been implicated in the progression of cellular aging through a multitude of studies that connect increased mitochondrial dysfunction, such as increased reactive oxygen species production and decreased ATP synthesis, with skeletal muscle undergoing sarcopenia. Studies reveal an inverse relationship between mitochondrial biogenesis and aging such that as an individual increases in age, mitochondrial function, and content decreases. This review aims to summarize the relationship of mitochondria with skeletal muscle function, the regulation of mitochondrial biogenesis, and the alterations in skeletal muscle and mitochondrial function that result due to the aging process. (C) 2009 IUBMB
引用
收藏
页码:201 / 214
页数:14
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