昼夜节律
生物
营养过剩
脂质代谢
脂肪生成
甾醇调节元件结合蛋白
内生
过氧化物酶体
激活剂(遗传学)
过氧化物酶体增殖物激活受体
内分泌学
内科学
生物钟
细胞生物学
生物化学
受体
胆固醇
肥胖
甾醇
医学
作者
Dongyin Guan,Ying Xiong,Patrícia Cristine Borck,Cholsoon Jang,Paschalis‐Thomas Doulias,Romeo Papazyan,Bin Fang,Chunjie Jiang,Yuxiang Zhang,Erika R. Briggs,Wenxiang Hu,David J. Steger,Harry Ischiropoulos,Joshua D. Rabinowitz,Mitchell A. Lazar
出处
期刊:Cell
[Cell Press]
日期:2018-08-01
卷期号:174 (4): 831-842.e12
被引量:146
标识
DOI:10.1016/j.cell.2018.06.031
摘要
Overnutrition disrupts circadian metabolic rhythms by mechanisms that are not well understood. Here, we show that diet-induced obesity (DIO) causes massive remodeling of circadian enhancer activity in mouse liver, triggering synchronous high-amplitude circadian rhythms of both fatty acid (FA) synthesis and oxidation. SREBP expression was rhythmically induced by DIO, leading to circadian FA synthesis and, surprisingly, FA oxidation (FAO). DIO similarly caused a high-amplitude circadian rhythm of PPARα, which was also required for FAO. Provision of a pharmacological activator of PPARα abrogated the requirement of SREBP for FAO (but not FA synthesis), suggesting that SREBP indirectly controls FAO via production of endogenous PPARα ligands. The high-amplitude rhythm of PPARα imparted time-of-day-dependent responsiveness to lipid-lowering drugs. Thus, acquisition of rhythmicity for non-core clock components PPARα and SREBP1 remodels metabolic gene transcription in response to overnutrition and enables a chronopharmacological approach to metabolic disorders.
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