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Interaction Between the Central and Peripheral Effects of Insulin in Controlling Hepatic Glucose Metabolism in the Conscious Dog

机译:胰岛素在控制清醒犬肝脏葡萄糖代谢中的中枢和外围作用之间的相互作用

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摘要

The importance of hypothalamic insulin action to the regulation of hepatic glucose metabolism in the presence of a normal liver/ brain insulin ratio (3:1) is unknown. Thus, we assessed the role of central insulin action in the response of the liver to normal physiologic hyperinsulinemia over 4 h. Using a pancreatic clamp, hepatic portal vein insulin delivery was increased three- or eightfold in the conscious dog. Insulin action was studied in the presence or absence of intracerebroventricularly mediated blockade of hypothalamic insulin action. Euglycemia was maintained, and glucagon was clamped at basal. Both the molecular and metabolic aspects of insulin action were assessed. Blockade of hypothalamic insulin signaling did not alter the insulin-mediated suppression of hepatic gluconeogenic gene transcription but blunted the induction of glucokinase gene transcription and completely blocked the inhibition of glycogen synthase kinase-3β gene transcription. Thus, central and peripheral insulin action combined to control some, but not other, hepatic enzyme programs. Nevertheless, inhibition of hypothalamic insulin action did not alter the effects of the hormone on hepatic glucose flux (production or uptake). These data indicate that brain insulin action is not a determinant of the rapid (<4 h) inhibition of hepatic glucose metabolism caused by normal physiologic hyperinsulinemia in this large animal model.
机译:在正常肝/脑胰岛素比率(3:1)的情况下,下丘脑胰岛素作用对调节肝葡萄糖代谢的重要性尚不清楚。因此,我们评估了中枢胰岛素作用在超过4小时的肝脏对正常生理性高胰岛素血症的反应中的作用。使用胰腺钳,有意识的狗的肝门静脉胰岛素递送增加了三倍或八倍。在存在或不存在脑室内介导的下丘脑胰岛素作用阻滞的情况下研究胰岛素作用。维持血糖正常,并将胰高血糖素固定在基础部位。胰岛素作用的分子和代谢方面都进行了评估。下丘脑胰岛素信号传导的阻滞并没有改变胰岛素介导的肝糖异生基因转录的抑制,但使葡萄糖激酶基因转录的诱导减弱,并完全阻止了糖原合酶激酶-3β基因转录的抑制。因此,中枢和外周的胰岛素作用相结合以控制一些而非其他肝酶程序。尽管如此,下丘脑胰岛素作用的抑制并没有改变激素对肝葡萄糖通量的影响(产生或摄取)。这些数据表明,在这种大型动物模型中,脑部胰岛素作用不是正常生理高胰岛素血症引起的肝葡萄糖代谢快速(<4 h)抑制的决定因素。

著录项

  • 来源
    《Diabetes》 |2013年第1期|74-84|共11页
  • 作者单位

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee,Medical College of Georgia at Georgia Health Sciences University, Department of Cellular Biology and Anatomy, Augusta, Georgia;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Division of Surgical Research, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

    Vanderbilt University School of Medicine, Department of Molecular Physiology and Biophysics, Nashville, Tennessee;

  • 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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  • 入库时间 2022-08-18 03:46:21

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