| Literature DB >> 27076076 |
Baokun He1, Kazunari Nohara1, Noheon Park2, Yong-Sung Park1, Bobby Guillory3, Zhaoyang Zhao1, Jose M Garcia3, Nobuya Koike4, Cheng Chi Lee1, Joseph S Takahashi5, Seung-Hee Yoo1, Zheng Chen6.
Abstract
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.Entities:
Keywords: Nobiletin; circadian clock; clock amplitude-enhancing small molecule; metabolic syndrome; natural flavonoid; retinoid acid receptor-related orphan receptors (RORs)
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Year: 2016 PMID: 27076076 PMCID: PMC4832569 DOI: 10.1016/j.cmet.2016.03.007
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287