The Small Molecule Nobiletin Targets the Molecular Oscillator to Enhance Circadian Rhythms and Protect against Metabolic Syndrome

被引:390
作者
He, Baokun [1 ]
Nohara, Kazunari [1 ]
Park, Noheon [2 ]
Park, Yong-Sung [1 ]
Guillory, Bobby [3 ,4 ]
Zhao, Zhaoyang [1 ]
Garcia, Jose M. [3 ,4 ,7 ]
Koike, Nobuya [5 ]
Lee, Cheng Chi [1 ]
Takahashi, Joseph S. [2 ,6 ]
Yoo, Seung-Hee [1 ]
Chen, Zheng [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Biochem & Mol Biol, 6431 Fannin St, Houston, TX 77030 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Neurosci, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[3] Baylor Coll Med, Michael E DeBakey Vet Affairs Med Ctr, Ctr Translat Res Inflammatory Dis, MCL,Div Endocrinol Diabet & Metab, Houston, TX 77030 USA
[4] Baylor Coll Med, Huffington Ctr Aging, Dan L Duncan Canc Ctr, Dept Med & Mol & Cell Biol, Houston, TX 77030 USA
[5] Kyoto Prefectural Univ Med, Dept Physiol & Syst Biosci, Kyoto 6028566, Japan
[6] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
[7] Univ Washington, VA Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, 1660 South Columbian Way S-182-GRECC, Seattle, WA 98108 USA
关键词
ORPHAN NUCLEAR RECEPTOR; REV-ERB-ALPHA; HIGH-FAT DIET; ROR-GAMMA-T; INSULIN-RESISTANCE; CITRUS FLAVONOIDS; LIPID-METABOLISM; GENE-EXPRESSION; CLOCK; MICE;
D O I
10.1016/j.cmet.2016.03.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:610 / 621
页数:12
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