He Baokun, Nohara Kazunari, Park Noheon, Park Yong-Sung, Guillory Bobby, Zhao Zhaoyang, Garcia Jose M, Koike Nobuya, Lee Cheng Chi, Takahashi Joseph S, Yoo Seung-Hee, Chen Zheng
Department of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston, 6431 Fannin Street, Houston, TX 77030, USA.
Department of Neuroscience, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Cell Metab. 2016 Apr 12;23(4):610-21. doi: 10.1016/j.cmet.2016.03.007.
Dysregulation of circadian rhythms is associated with metabolic dysfunction, yet it is unclear whether enhancing clock function can ameliorate metabolic disorders. In an unbiased chemical screen using fibroblasts expressing PER2::Luc, we identified Nobiletin (NOB), a natural polymethoxylated flavone, as a clock amplitude-enhancing small molecule. When administered to diet-induced obese (DIO) mice, NOB strongly counteracted metabolic syndrome and augmented energy expenditure and locomotor activity in a Clock gene-dependent manner. In db/db mutant mice, the clock is also required for the mitigating effects of NOB on metabolic disorders. In DIO mouse liver, NOB enhanced clock protein levels and elicited pronounced gene expression remodeling. We identified retinoid acid receptor-related orphan receptors as direct targets of NOB, revealing a pharmacological intervention that enhances circadian rhythms to combat metabolic disease via the circadian gene network.
昼夜节律失调与代谢功能障碍有关,但尚不清楚增强生物钟功能是否能改善代谢紊乱。在一项使用表达PER2::Luc的成纤维细胞进行的无偏化学筛选中,我们鉴定出一种天然多甲氧基黄酮——川陈皮素(NOB),它是一种能增强生物钟振幅的小分子。给饮食诱导肥胖(DIO)小鼠服用NOB后,它能以生物钟基因依赖的方式强烈对抗代谢综合征,并增加能量消耗和运动活动。在db/db突变小鼠中,生物钟对于NOB减轻代谢紊乱的作用也是必需的。在DIO小鼠肝脏中,NOB提高了生物钟蛋白水平,并引发了明显的基因表达重塑。我们鉴定出维甲酸受体相关孤儿受体是NOB的直接靶点,揭示了一种通过生物钟基因网络增强昼夜节律以对抗代谢疾病的药理学干预方法。