The systemic role of SIRT1 in exercise mediated adaptation

被引:58
|
作者
Radak, Zsolt [1 ,2 ,3 ]
Suzuki, Katsuhiko [2 ]
Posa, Aniko [3 ]
Petrovszky, Zita [3 ]
Koltai, Erika [1 ]
Boldogh, Istvan [4 ]
机构
[1] Univ Phys Educ, Res Inst Sport Sci, Budapest, Hungary
[2] Waseda Univ, Fac Sport Sci, Saitama 3591192, Japan
[3] Univ Szeged, Szeged, Hungary
[4] Univ Texas Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA
来源
REDOX BIOLOGY | 2020年 / 35卷
关键词
NICOTINAMIDE-ADENINE-DINUCLEOTIDE; SKELETAL-MUSCLE; MITOCHONDRIAL BIOGENESIS; PHYSICAL-EXERCISE; OXIDATIVE STRESS; NITRIC-OXIDE; P53-INDUCIBLE REGULATOR; RESVERATROL; RAT; EXPRESSION;
D O I
10.1016/j.redox.2020.101467
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
Cellular energy demands are readily changed during physical exercise resulting in adaptive responses by signaling proteins of metabolic processes, including the NAD+ dependent lysine deacetylase SIRT1. Regular exercise results in systemic adaptation that restores the level of SIRT1 in the kidney, liver, and brain in patients with neurodegenerative diseases, and thereby normalizes cellular metabolic processes to attenuate the severity of these diseases. In skeletal muscle, over-expression of SIRT1 results in enhanced numbers of myonuclei improves the repair process after injury and is actively involved in muscle hypertrophy by up-regulating anabolic and downregulating catabolic processes. The present review discusses the different views of SIRT1 dependent deacetylation of PGC-α. © 2020 The Authors
引用
收藏
页数:7
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