Caloric restriction and the aging process: a critique

被引:119
作者
Sohal, Rajindar S. [1 ]
Forster, Michael J. [2 ]
机构
[1] Univ So Calif, Dept Pharmacol & Pharmaceut Sci, Los Angeles, CA 90089 USA
[2] Univ N Texas, Hlth Sci Ctr, Dept Pharmacol & Neurosci, Ft Worth, TX 76107 USA
基金
美国国家卫生研究院;
关键词
Dietary restriction; Aging; Energy restriction; Life span; Oxidative stress; Free radicals; Mechanisms of aging; Redox state; Caloric restriction; Redox stress hypothesis of aging; FREE-RADICAL THEORY; LIFE-SPAN EXTENSION; GLUTATHIONE REDOX STATE; 2 DIFFERENT STRAINS; FLUORESCENT AGE PIGMENT; SPRAGUE-DAWLEY RAT; DIETARY RESTRICTION; OXIDATIVE STRESS; FOOD RESTRICTION; SUPEROXIDE-DISMUTASE;
D O I
10.1016/j.freeradbiomed.2014.05.015
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
The main objective of this review is to provide an appraisal of the current status of the relationship between energy intake and the life span of animals. The concept that a reduction in food intake, or caloric restriction (CR), retards the aging process, delays the age-associated decline in physiological fitness, and extends the life span of organisms of diverse phylogenetic groups is one of the leading paradigms in gerontology. However, emerging evidence disputes some of the primary tenets of this conception. One disparity is that the CR-related increase in longevity is not universal and may not even be shared among different strains of the same species. A further misgiving is that the control animals, fed ad libitum (AL), become overweight and prone to early onset of diseases and death, and thus may not be the ideal control animals for studies concerned with comparisons of longevity. Reexamination of body weight and longevity data from a study involving over 60,000 mice and rats, conducted by a National Institute on Aging-sponsored project, suggests that CR-related increase in life span of specific genotypes is directly related to the gain in body weight under the AL feeding regimen. Additionally, CR in mammals and "dietary restriction" in organisms such as Drosophila are dissimilar phenomena, albeit they are often presented to be the very same. The latter involves a reduction in yeast rather than caloric intake, which is inconsistent with the notion of a common, conserved mechanism of CR action in different species. Although specific mechanisms by which CR affects longevity are not well understood, existing evidence supports the view that CR increases the life span of those particular genotypes that develop energy imbalance owing to AL feeding. In such groups, CR lowers body temperature, rate of metabolism, and oxidant production and retards the age-related pro-oxidizing shift in the redox state. (C) 2014 The Authors. Published by Elsevier Inc.
引用
收藏
页码:366 / 382
页数:17
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