Facts and controversies in our understanding of how caloric restriction impacts the mitochondrion

被引:33
作者
Gouspillou, Gilles [1 ]
Hepple, Russell T. [1 ]
机构
[1] McGill Univ, Dept Kinesiol, Ctr Hlth, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
Caloric restriction; Aging; Mitochondria; Sirtuin; PGC-1a; Sarcopenia; OXYGEN SPECIES PRODUCTION; OXIDATIVE DNA-DAMAGE; TRANSCRIPTIONAL COACTIVATOR PGC-1-ALPHA; PERMEABILITY TRANSITION PORE; HYDROGEN-PEROXIDE PRODUCTION; ELECTRON-TRANSPORT CHAIN; SOMATIC MTDNA MUTATIONS; FREE-RADICAL GENERATION; FATTY-ACID-COMPOSITION; LYSOSOMAL AXIS THEORY;
D O I
10.1016/j.exger.2013.03.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Caloric restriction (CR) has pronounced benefits in promoting healthy aging. Amongst the most frequently implicated physiological mechanisms implicated in this benefit is altered mitochondrial function. Whereas a reduction in mitochondrial reactive oxygen species (ROS) production is a widely consistent effect of CR, an increase in mitochondrial biogenesis, which is accepted by many as fact, is contradicted on several levels, most critically by a lack of increase in mitochondrial protein synthesis rate in vivo. Furthermore, an increase in PGC-1 alpha protein and markers of mitochondrial content with CR is a highly variable observation between studies. On the other hand, deacetylation of several mitochondrial proteins by the sirtuin, Sirt3, is an increasingly reported observation and at least so far, this observation is consistent between studies. Notwithstanding this point, the controversies evident in the published literature underscore the significant questions that remain in our understanding of how CR impacts the mitochondrion and suggest we have yet to fully understand the complexities herein. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1075 / 1084
页数:10
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