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Regulation of circadian behaviour and metabolism by synthetic REV-ERB agonists

机译:合成REV-ERB激动剂对昼夜节律行为和代谢的调节

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摘要

Synchronizing rhythms of behaviour and metabolic processes is important for cardiovascular health and preventing metabolic diseases. The nuclear receptors REV-ERB-α and REV-ERB- p have an integral role in regulating the expression of core clock proteins driving rhythms in activity and metabolism. Here we describe the identification of potent synthetic REV-ERB agonists with in vivo activity. Administration of synthetic REV-ERB ligands alters circadian behaviour and the circadian pattern of core clock gene expression in the hypothalami of mice. The circadian pattern of expression of an array of metabolic genes in the liver, skeletal muscle and adipose tissue was also altered, resulting in increased energy expenditure. Treatment of diet-induced obese mice with a REV-ERB agonist decreased obesity by reducing fat mass and markedly improving dyslipidaemia and hyperglycaemia. These results indicate that synthetic REV-ERB ligands that pharmacologically target the circadian rhythm may be beneficial in the treatment of sleep disorders as well as metabolic diseases.
机译:同步行为和代谢过程的节律对于心血管健康和预防代谢疾病很重要。核受体REV-ERB-α和REV-ERB-p在调节驱动活动和代谢节律的核心时钟蛋白的表达中起着不可或缺的作用。在这里,我们描述了具有体内活性的有效合成REV-ERB激动剂的鉴定。合成REV-ERB配体的施用改变了小鼠下丘脑的生物钟行为和核心时钟基因表达的生物钟模式。肝脏,骨骼肌和脂肪组织中一系列代谢基因的昼夜节律表达也发生了改变,导致能量消耗增加。用REV-ERB激动剂治疗饮食诱发的肥胖小鼠,可通过减少脂肪量和显着改善血脂异常和高血糖症来降低肥胖。这些结果表明,以药理学为目标的昼夜节律的合成REV-ERB配体可能对治疗睡眠障碍和代谢性疾病有益。

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  • 来源
    《Nature》 |2012年第7396期|p.62-68|共7页
  • 作者单位

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Translational Research Institute, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Translational Research Institute, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Translational Research Institute, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Howard Hughes Medical Institute and Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;

    Howard Hughes Medical Institute and Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;

    Department of Metabolism and Aging, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Translational Research Institute, The Scripps Research Institute, Jupiter, Florida 33458, USA;

    Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, Florida 33458, USA,Center for Diabetes and Metabolic Diseases, The Scripps Research Institute, Jupiter, Florida 33458, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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