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The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity

机译:视交叉上核控制昼夜能量代谢和肝胰岛素敏感性。

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摘要

Disturbances in the circadian system are associated with the development of type 2 diabetes mellitus. Here, we studied the direct contribution of the suprachiasmatic nucleus (SCN), the central pacemaker in the circadian system, in the development of insulin resistance. Exclusive bilateral SCN lesions in male C57B1/6J mice, as verified by immunochemistry, showed a small but significant increase in body weight (+17%), which was accounted for by an increase in fat mass. In contrast, mice with collateral damage to the ventromedial hypothalamus and paraventricular nucleus showed severe obesity and insulin resistance. Mice with exclusive SCN ablation revealed a loss of circadian rhythm in activity, oxygen consumption, and food intake. Hyperinsulinemic-euglycemic clamp analysis 8 weeks after lesioning showed that the glucose infusion rate was significantly lower in SCN lesioned mice compared with sham-operated mice (-63%). Although insulin potently inhibited endogenous glucose production (-84%), this was greatly reduced in SCN lesioned mice (-7%), indicating severe hepatic insulin resistance. Our data show that SCN malfunctioning plays an important role in the disturbance of energy balance and suggest that an absence of central clock activity, in a genetically intact animal, may lead to the development of insulin resistance.
机译:昼夜节律紊乱与2型糖尿病的发展有关。在这里,我们研究了昼夜视神经上枢(SCN)(昼夜节律系统中的中心起搏器)对胰岛素抵抗发展的直接贡献。免疫化学方法证实,雄性C57B1 / 6J小鼠的双侧SCN唯一病变显示出体重的微小但显着增加(+ 17%),这是由脂肪量增加引起的。相反,对腹侧下丘脑和脑室旁核有附带损害的小鼠表现出严重的肥胖和胰岛素抵抗。进行SCN独家消融的小鼠在活动,氧气消耗和食物摄入方面昼夜节律消失。损伤后8周的高胰岛素-正常血糖钳夹分析显示,与假手术小鼠相比,SCN损伤小鼠的葡萄糖输注速率明显更低(-63%)。尽管胰岛素有效地抑制了内源性葡萄糖的产生(-84%),但在SCN损伤小鼠中却大大降低了内源性葡萄糖的产生(-7%),表明肝胰岛素抵抗严重。我们的数据表明,SCN功能异常在能量平衡紊乱中起着重要作用,并暗示在基因上完整的动物中缺乏中央时钟活动可能导致胰岛素抵抗的发展。

著录项

  • 来源
    《Diabetes》 |2013年第4期|1102-1108|共7页
  • 作者单位

    Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands ,Department of Endocrinology and Metabolic Disorders, Leiden University Medical Center, Leiden, the Netherlands;

    Department of Human Genetics, Lei-den University Medical Center, Leiden, the Netherlands;

    Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands;

    Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands;

    Department of Human Genetics, Lei-den University Medical Center, Leiden, the Netherlands;

    Department of Endocrinology and Metabo-lism, Academic Medical Center, Amsterdam, the Netherlands;

    Department of Endocrinology and Metabo-lism, Academic Medical Center, Amsterdam, the Netherlands, De-partment of Hypothalamic Integration Mechanisms, Netherlands Institute for Neuroscience, Amsterdam, the Netherlands.;

    Department of Endocrinology and Metabolic Disorders, Leiden University Medical Center, Leiden, the Netherlands;

    Department of Human Genetics, Lei-den University Medical Center, Leiden, the Netherlands;

    Department of Endocrinology and Metabolic Disorders, Leiden University Medical Center, Leiden, the Netherlands ,Department of Endocrinology and Metabo-lism, Academic Medical Center, Amsterdam, the Netherlands;

    Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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