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
相关论文
共 244 条
  • [71] FROY O, 2009, ENDOCR REV IN PRESS
  • [72] Interrelations among feeding, circadian rhythms and ageing
    Froy, Oren
    Miskin, Ruth
    [J]. PROGRESS IN NEUROBIOLOGY, 2007, 82 (03) : 142 - 150
  • [73] Froy O, 2007, MOL IMMUNOL, V44, P1954, DOI 10.1016/j.molimm.2006.09.026
  • [74] Long-lived αMUPA transgenic mice exhibit pronounced circadian rhythms
    Froy, Oren
    Chapnik, Nava
    Miskin, Ruth
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2006, 291 (05): : E1017 - E1024
  • [75] Effect of intermittent fasting on circadian rhythms in mice depends on feeding time
    Froy, Oren
    Chapnik, Nava
    Miskin, Ruth
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 2009, 130 (03) : 154 - 160
  • [76] The circadian gene Period2 plays an important role in tumor suppression and DNA damage response in vivo
    Fu, LN
    Pelicano, H
    Liu, JS
    Huang, P
    Lee, CC
    [J]. CELL, 2002, 111 (01) : 41 - 50
  • [77] Aging in the circadian system: Considerations for health, disease prevention and longevity
    Gibson, Erin M.
    Williams, Wilbur P., III
    Kriegsfeld, Lance J.
    [J]. EXPERIMENTAL GERONTOLOGY, 2009, 44 (1-2) : 51 - 56
  • [78] Metabolic adaptations to fasting and chronic caloric restriction in heart, muscle, and liver do not include changes in AMPK activity
    Gonzalez, AA
    Kumar, R
    Mulligan, JD
    Davis, AJ
    Weindruch, R
    Saupe, KW
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2004, 287 (05): : E1032 - E1037
  • [79] EFFECTS OF INTERMITTENT FEEDING UPON BODY-WEIGHT AND LIFE-SPAN IN INBRED MICE - INTERACTION OF GENOTYPE AND AGE
    GOODRICK, CL
    INGRAM, DK
    REYNOLDS, MA
    FREEMAN, JR
    CIDER, N
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 1990, 55 (01) : 69 - 87
  • [80] The dorsomedial hypothalamic nucleus is critical for the expression of food- entrainable circadian rhythms
    Gooley, JJ
    Schomer, A
    Saper, CB
    [J]. NATURE NEUROSCIENCE, 2006, 9 (03) : 398 - 407