4.8 Review

Circadian rhythms, sleep, and metabolism

期刊

JOURNAL OF CLINICAL INVESTIGATION
卷 121, 期 6, 页码 2133-2141

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI46043

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资金

  1. NIDDK [T32 DK007169]
  2. NIH [P01 AG011412, R01HL097817-01]
  3. American Diabetes Association, Chicago Biomedical Consortium
  4. Juvenile Diabetes Research Foundation
  5. University of Chicago Diabetes Research and Training Center [P60 DK020595]
  6. Amylin Pharmaceuticals
  7. Merck Co.
  8. Life Sciences Institute of the University of Michigan

向作者/读者索取更多资源

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.

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