4.8 Article

Time-Restricted Feeding Prevents Obesity and Metabolic Syndrome in Mice Lacking a Circadian Clock

期刊

CELL METABOLISM
卷 29, 期 2, 页码 303-+

出版社

CELL PRESS
DOI: 10.1016/j.cmet.2018.08.004

关键词

-

资金

  1. American Federation for Aging Research (AFAR) [M14322]
  2. NIH [DK115214, P30 CA014195, P30 EY019005, P50 GM085764, R24 DK080506]
  3. Glenn Center for Aging, Leona M. and Harry B. Helmsley Charitable Trust [2012-PG-MED002]
  4. American Diabetes Association [7-12-MN-64]
  5. American Heart Association Career Development Award [18CDA34110292]
  6. Philippe Foundation Inc., New York
  7. Salk Institute

向作者/读者索取更多资源

Increased susceptibility of circadian clock mutant mice to metabolic diseases has led to the idea that a molecular clock is necessary for metabolic homeostasis. However, these mice often lack a normal feeding-fasting cycle. We tested whether time-restricted feeding (TRF) could prevent obesity and metabolic syndrome in whole-body Cry1; Cry2 and in liver-specific Bmal1 and Rev-erb alpha/beta knockout mice. When provided access to food ad libitum, these mice rapidly gained weight and showed genotype-specific metabolic defects. However, when fed the same diet under TRF (food access restricted to 10 hr during the dark phase) they were protected from excessive weight gain and metabolic diseases. Transcriptome and metabolome analyses showed that TRF reduced the accumulation of hepatic lipids and enhanced cellular defenses against metabolic stress. These results suggest that the circadian clock maintains metabolic homeostasis by sustaining daily rhythms in feeding and fasting and by maintaining balance between nutrient and cellular stress responses.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据