Effect of feeding regimens on circadian rhythms: Implications for aging and longevity

被引:94
|
作者
Froy, Oren [1 ]
Miskin, Ruth [2 ]
机构
[1] Hebrew Univ Jerusalem, Inst Biochem Food Sci & Nutr, Robert H Smith Fac Agr Food & Environm, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
来源
AGING-US | 2010年 / 2卷 / 01期
关键词
clock; circadian rhythms; caloric restriction; intermittent fasting; metabolism; alpha MUPA; life span; aging; REV-ERB-ALPHA; ACTIVATED PROTEIN-KINASE; DORSOMEDIAL HYPOTHALAMIC NUCLEUS; CHRONIC CALORIC RESTRICTION; FOOD-ANTICIPATORY ACTIVITY; CLOCK GENE-EXPRESSION; MUPA TRANSGENIC MICE; ARNT-LIKE PROTEIN-1; SUPRACHIASMATIC NUCLEUS; DIETARY RESTRICTION;
D O I
10.18632/aging.100116
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Increased longevity and improved health can be achieved in mammals by two feeding regimens, caloric restriction (CR), which limits the amount of daily calorie intake, and intermittent fasting (IF), which allows the food to be available ad libitum every other day. The precise mechanisms mediating these beneficial effects are still unresolved. Resetting the circadian clock is another intervention that can lead to increased life span and well being, while clock disruption is associated with aging and morbidity. Currently, a large body of evidence links circadian rhythms with metabolism and feeding regimens. In particular, CR, and possibly also IF, can entrain the master clock located in the suprachiasmatic nuclei (SCN) of the brain hypothalamus. These findings raise the hypothesis that the beneficial effects exerted by these feeding regimens could be mediated, at least in part, through resetting of the circadian clock, thus leading to synchrony in metabolism and physiology. This hypothesis is reinforced by a transgenic mouse model showing spontaneously reduced eating alongside robust circadian rhythms and increased life span. This review will summarize recent findings concerning the relationships between feeding regimens, circadian rhythms, and metabolism with implications for ageing attenuation and life span extension.
引用
收藏
页码:7 / 27
页数:21
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