首页> 外文期刊>The journals of gerontology.Series A. Biological sciences and medical sciences >Insulin signaling cascade in the hearts of long-lived growth hormone receptor knockout mice: effects of calorie restriction.
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Insulin signaling cascade in the hearts of long-lived growth hormone receptor knockout mice: effects of calorie restriction.

机译:长寿命生长激素受体敲除小鼠心脏中的胰岛素信号传导级联:限制卡路里的作用。

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Calorie restriction (CR) improves insulin sensitivity and increases life span in normal but not in long-lived growth hormone-resistant knockout (GHRKO) mice. In this study, we examined interactive effects of GH resistance and long-term CR on cardiac insulin action. GHRKO mice exhibited marked increases in the insulin-induced phosphorylation of the insulin receptor (IR), insulin receptor substrate-1 (IRS-1), Akt, and ERK1/2 along with elevated insulin-stimulated IRS-1-associated regulatory subunit of phosphatidylinositol 3-kinase in the heart. These changes were associated with elevated protein levels of IR, IRS-1, and Akt and with a down-regulation of cardiac glucose transporter 4 (GLUT4). In normal mice, CR induced an important increase in the phosphorylation of cardiac Akt without elevation of Akt protein, reaching activation levels similar to those seen in GHRKO mice. This change may be cardioprotective and thus contribute to increased longevity in response to CR. Interestingly, the insulin signaling cascade in the heart of GHRKO mice was unaffected by CR.
机译:卡路里限制(CR)可改善正常情况下的胰岛素敏感性并延长寿命,但不能延长长寿的生长激素抵抗性基因敲除(GHRKO)小鼠的寿命。在这项研究中,我们检查了GH抵抗力和长期CR对心脏胰岛素作用的相互作用。 GHRKO小鼠在胰岛素诱导的胰岛素受体(IR),胰岛素受体底物1(IRS-1),Akt和ERK1 / 2的磷酸化中显着增加,并且胰岛素刺激的IRS-1相关调节亚基升高。心脏中的磷脂酰肌醇3激酶。这些变化与IR,IRS-1和Akt的蛋白质水平升高以及心脏葡萄糖转运蛋白4(GLUT4)的下调有关。在正常小鼠中,CR诱导了心脏Akt磷酸化的重要增加,而Akt蛋白却没有升高,达到了与GHRKO小鼠相似的激活水平。这种变化可能具有心脏保护作用,因此有助于响应CR延长寿命。有趣的是,GHRKO小鼠心脏中的胰岛素信号传导级联不受CR影响。

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