通过营养挑战重新编程昼夜时钟
Kristin L Eckel-Mahan1, Vishal R Patel2, Sara de Mateo1
1Center for Epigenetics and Metabolism, Department of Biological Chemistry, University of California, Irvine, Irvine, CA 92697, USA.
Cell
|December 24, 2013
概括
高脂肪饮食显著改变肝脏新陈代谢和每日生物钟. 这些变化是由营养而不是肥胖驱动的,会扰乱正常的节律,但是可逆的.
科学领域:
- 代谢途径 代谢途径
- 时间生物学 时间生物学
- 肝脏时钟调节 肝脏时钟调节
背景情况:
- 昼夜节律和细胞代谢密切相关.
- 饮食干预可以深刻影响生理过程.
研究的目的:
- 为了研究高脂肪饮食 (HFD) 如何重组肝脏代谢途径和肝脏时钟.
- 为了阐明饮食诱导的时钟改造背后的分子机制.
- 为了确定营养挑战或肥胖是否驱动这些时钟变化.
主要方法:
- 对HFD反应中的代谢途径和转录基因数据的分析.
- 对 CLOCK:BMAL1 染色质招募的调查.
- 评估PPARγ在饮食引起的时钟变化中的作用.
- 区分营养挑战与肥胖的影响.
主要成果:
- HFD导致肝脏代谢途径和肝脏时钟的显著重组.
- HFD诱导了新的振荡转录,破坏了协调的振荡.
- 损坏的CLOCK:BMAL1招募和循环PPARγ激活介于重新编程.
- 营养挑战,而不是肥胖,是重编程时钟的主要驱动因素.
结论:
- 饮食诱导的肝脏时钟的重编程是相当大的,涉及到特定的分子机制.
- 肝脏时钟的反应主要是对营养挑战,其影响是可逆的.
- 了解这些动态对于代谢和昼夜健康至关重要.
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