Circadian rhythms, sleep, and metabolism

被引:483
作者
Huang, Wenyu [1 ,2 ]
Ramsey, Kathryn Moynihan [1 ,2 ]
Marcheva, Biliana [1 ,2 ]
Bass, Joseph [1 ,2 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Neurobiol & Physiol, Evanston, IL 60208 USA
关键词
ARNT-LIKE PROTEIN-1; REV-ERB-ALPHA; HIGH-FAT DIET; SUPRACHIASMATIC NUCLEUS; FOOD-INTAKE; GLUCOSE-HOMEOSTASIS; GENE-EXPRESSION; CLOCK GENE; PERIPHERAL-TISSUES; ENERGY HOMEOSTASIS;
D O I
10.1172/JCI46043
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The discovery of the genetic basis for circadian rhythms has expanded our knowledge of the temporal organization of behavior and physiology. The observations that the circadian gene network is present in most living organisms from eubacteria to humans, that most cells and tissues express autonomous clocks, and that disruption of clock genes results in metabolic dysregulation have revealed interactions between metabolism and circadian rhythms at neural, molecular, and cellular levels. A major challenge remains in understanding the interplay between brain and peripheral clocks and in determining how these interactions promote energy homeostasis across the sleep-wake cycle. In this Review, we evaluate how investigation of molecular timing may create new opportunities to understand and develop therapies for obesity and diabetes.
引用
收藏
页码:2133 / 2141
页数:9
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