4.6 Article

Chronic mild stress alters circadian expressions of molecular clock genes in the liver

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00388.2012

关键词

stress; liver clock; metabolic disorders; hypothalamus-pituitary-adrenal axis

资金

  1. Japan Society for the Promotion of Science [23591293, B2, 15390282]
  2. Global-COE from the Ministry of Education, Culture, Sports, Science and Technology of Japan
  3. Grants-in-Aid for Scientific Research [23591293, 23591294, 23791011, 24659439, 23390238, 22126006, 15390282] Funding Source: KAKEN

向作者/读者索取更多资源

Takahashi K, Yamada T, Tsukita S, Kaneko K, Shirai Y, Munakata Y, Ishigaki Y, Imai J, Uno K, Hasegawa Y, Sawada S, Oka Y, Katagiri H. Chronic mild stress alters circadian expressions of molecular clock genes in the liver. Am J Physiol Endocrinol Metab 304: E301-E309, 2013. First published December 4, 2012; doi:10.1152/ajpendo.00388.2012.-Chronic stress is well known to affect metabolic regulation. However, molecular mechanisms interconnecting stress response systems and metabolic regulations have yet to be elucidated. Various physiological processes, including glucose/lipid metabolism, are regulated by the circadian clock, and core clock gene dysregulation reportedly leads to metabolic disorders. Glucocorticoids, acting as end- effectors of the hypothalamus-pituitary-adrenal (HPA) axis, entrain the circadian rhythms of peripheral organs, including the liver, by phase-shifting core clock gene expressions. Therefore, we examined whether chronic stress affects circadian expressions of core clock genes and metabolism-related genes in the liver using the chronic mild stress (CMS) procedure. In BALB/c mice, CMS elevated and phase-shifted serum corticosterone levels, indicating overactivation of the HPA axis. The rhythmic expressions of core clock genes, e.g., Clock, Npas2, Bmal1, Per1, and Cry1, were altered in the liver while being completely preserved in the hypothalamic suprachiasmatic nuculeus (SCN), suggesting that the SCN is not involved in alterations in hepatic core clock gene expressions. In addition, circadian patterns of glucose and lipid metabolism-related genes, e.g., peroxisome proliferator activated receptor (Ppar) alpha, Ppar gamma-1, Ppar gamma-coactivator-1 alpha, and phosphoenolepyruvate carboxykinase, were also disturbed by CMS. In contrast, in C57BL/6 mice, the same CMS procedure altered neither serum corticosterone levels nor rhythmic expressions of hepatic core clock genes and metabolism-related genes. Thus, chronic stress can interfere with the circadian expressions of both core clock genes and metabolism-related genes in the liver possibly involving HPA axis overactivation. This mechanism might contribute to metabolic disorders in stressful modern societies.

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