Lamia Katja A, Storch Kai-Florian, Weitz Charles J
Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2008 Sep 30;105(39):15172-7. doi: 10.1073/pnas.0806717105. Epub 2008 Sep 8.
Mammals have circadian clocks in peripheral tissues, but there is no direct evidence of their physiological importance. Unlike the suprachiasmatic nucleus clock that is set by light and drives rest-activity and fasting-feeding cycles, peripheral clocks are set by daily feeding, suggesting that at least some contribute metabolic regulation. The liver plays a well known role in glucose homeostasis, and we report here that mice with a liver-specific deletion of Bmal1, an essential clock component, exhibited hypoglycemia restricted to the fasting phase of the daily feeding cycle, exaggerated glucose clearance, and loss of rhythmic expression of hepatic glucose regulatory genes. We conclude that the liver clock is important for buffering circulating glucose in a time-of-day-dependent manner. Our findings suggest that the liver clock contributes to homeostasis by driving a daily rhythm of hepatic glucose export that counterbalances the daily cycle of glucose ingestion resulting from the fasting-feeding cycle.
哺乳动物的外周组织中有昼夜节律时钟,但尚无直接证据表明其具有生理重要性。与由光设定并驱动休息-活动和禁食-进食周期的视交叉上核时钟不同,外周时钟由每日进食设定,这表明至少有一些外周时钟参与代谢调节。肝脏在葡萄糖稳态中发挥着众所周知的作用,我们在此报告,肝脏特异性缺失生物钟重要组成部分Bmal1的小鼠,在每日进食周期的禁食阶段出现低血糖,葡萄糖清除率过高,且肝脏葡萄糖调节基因的节律性表达丧失。我们得出结论,肝脏生物钟对于以每日时间依赖的方式缓冲循环葡萄糖很重要。我们的研究结果表明,肝脏生物钟通过驱动肝脏葡萄糖输出的每日节律来促进稳态,这种节律可抵消由禁食-进食周期导致的葡萄糖摄入的每日循环。