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      The small molecule Nobiletin targets the molecular oscillator to enhance circadian rhythms and protect against metabolic syndrome

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          SUMMARY

          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 (CEM). 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 (RORs) as direct targets of NOB, revealing a pharmacological intervention that enhances circadian rhythms to combat metabolic disease via the circadian gene network.

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          Author and article information

          Journal
          101233170
          32527
          Cell Metab
          Cell Metab.
          Cell metabolism
          1550-4131
          1932-7420
          23 March 2016
          12 April 2016
          12 April 2017
          : 23
          : 4
          : 610-621
          Affiliations
          [1 ]Department of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston, 6431 Fannin St., Houston, TX 77030
          [2 ]Department of Neuroscience, The University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390
          [3 ]Division of Endocrinology, Diabetes and Metabolism, MCL, Center for Translational Research in Inflammatory Diseases, Michael E. DeBakey Veterans Affairs Medical Center, Dept. of Medicine, and Molecular and Cell Biology, Dan L. Duncan Cancer Center, Huffington Center on Aging, Baylor College of Medicine, Houston, TX 77030, USA
          [4 ]Department of Physiology and Systems Bioscience, Kyoto Prefectural University of Medicine, Kyoto, 602-8566, Japan
          [5 ]Howard Hughes Medical Institute, The University of Texas Southwestern Medical Center, Dallas, TX 75390
          Author notes
          [* ]To whom correspondence should be addressed: Zheng.chen.1@ 123456uth.tmc.edu . Phone: (Office) 713-500-6284; (Mobile) 214-336-6824
          Article
          PMC4832569 PMC4832569 4832569 nihpa771136
          10.1016/j.cmet.2016.03.007
          4832569
          27076076
          06b24a86-6656-47cf-adfa-2988e54931c8
          History
          Categories
          Article

          clock amplitude-enhancing small molecule,Circadian clock,Nobiletin,retinoid acid receptor-related orphan receptors (RORs),metabolic syndrome,natural flavonoid

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