| Literature DB >> 24506873 |
Yaarit Adamovich1, Liat Rousso-Noori1, Ziv Zwighaft1, Adi Neufeld-Cohen1, Marina Golik1, Judith Kraut-Cohen1, Miao Wang2, Xianlin Han2, Gad Asher3.
Abstract
Circadian clocks play a major role in orchestrating daily physiology, and their disruption can evoke metabolic diseases such as fatty liver and obesity. To study the role of circadian clocks in lipid homeostasis, we performed an extensive lipidomic analysis of liver tissues from wild-type and clock-disrupted mice either fed ad libitum or night fed. To our surprise, a similar fraction of lipids (∼17%) oscillated in both mouse strains, most notably triglycerides, but with completely different phases. Moreover, several master lipid regulators (e.g., PPARα) and enzymes involved in triglyceride metabolism retained their circadian expression in clock-disrupted mice. Nighttime restricted feeding shifted the phase of triglyceride accumulation and resulted in ∼50% decrease in hepatic triglyceride levels in wild-type mice. Our findings suggest that circadian clocks and feeding time dictate the phase and levels of hepatic triglyceride accumulation; however, oscillations in triglycerides can persist in the absence of a functional clock.Entities:
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Year: 2014 PMID: 24506873 PMCID: PMC4261230 DOI: 10.1016/j.cmet.2013.12.016
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287