Mechanisms of the anti-aging and prolongevity effects of caloric restriction: evidence from studies of genetically modified animals

被引:18
作者
Hoshino, Shunsuke [1 ,2 ]
Kobayashi, Masaki [1 ,2 ]
Higami, Yoshikazu [1 ,2 ]
机构
[1] Tokyo Univ Sci, Fac Pharmaceut Sci, Lab Mol Pathol & Metab Dis, Noda, Chiba 2788510, Japan
[2] Tokyo Univ Sci, Res Inst Sci & Technol, Translat Res Ctr, Noda, Chiba 2788510, Japan
来源
AGING-US | 2018年 / 10卷 / 09期
基金
日本学术振兴会;
关键词
caloric restriction; aging; growth hormone/insulin-like growth factor 1; mitochondria/redox regulation; remodeling of white adipose tissue; LIFE-SPAN EXTENSION; WHITE ADIPOSE-TISSUE; FACTOR-I AXIS; DIETARY RESTRICTION; GENE-EXPRESSION; DWARF MICE; REDUCTION; LONGEVITY; STRESS; ADIPONECTIN;
D O I
10.18632/aging.101557
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It is widely accepted that caloric restriction (CR) extends lifespan and suppresses various pathophysiological changes. CR suppresses growth hormone/insulin-like growth factor signaling and mechanistic target of rapamycin complex 1 activity, activates sirtuin and enhances mitochondrial redox regulation, but the exact mechanisms are still under debate. In this review, we discuss the mechanisms of CR using evidence from studies of animals that were genetically modified according to recent advances in molecular and genetic technologies, from the viewpoint of the adaptive response hypothesis proposed by Holliday (1989). We then explain the beneficial actions of CR, classified according to whether they operate under feeding or fasting conditions.
引用
收藏
页码:2243 / 2251
页数:9
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