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首页> 外文期刊>FEBS letters. >Loss of mPer2 increases plasma insulin levels by enhanced glucose-stimulated insulin secretion and impaired insulin clearance in mice
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Loss of mPer2 increases plasma insulin levels by enhanced glucose-stimulated insulin secretion and impaired insulin clearance in mice

机译:mPer2的丢失会通过增强葡萄糖刺激的胰岛素分泌和损害小鼠的胰岛素清除率而增加血浆胰岛素水平

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摘要

The existence of peripheral oscillators has been shown, and they are critically important for organizing the metabolism of the whole body. Here we show that mice deficient in mPer2 markedly increase circulatory levels of insulin compared with wild type mice. Insulin secretion was more effectively stimulated by glucose, and alloxan, a glucose analogue, induced more severe hyperglycemia in mPer2-deficient mice. Hepatic insulin degrading enzyme (Ide) displayed an obvious day and night rhythm, which was impaired in mPer2-deficient mice, leading to a decrease in insulin clearance. Deficiency in mPer2 caused increased Clock expression and decreased expression of Mkp1 and Ide1, possibly underlying the observed phenotypes and suggesting that mPer2 plays a role in regulation of circulating insulin levels.
机译:已经显示出外围振荡器的存在,并且它们对于组织全身的新陈代谢至关重要。在这里,我们显示与野生型小鼠相比,mPer2缺乏的小鼠显着增加了胰岛素的循环水平。葡萄糖可更有效地刺激胰岛素分泌,而葡萄糖类似物四氧嘧啶可在mPer2缺乏症小鼠中引起更严重的高血糖症。肝胰岛素降解酶(Ide)表现出明显的昼夜节律,这在mPer2缺陷型小鼠中受损,导致胰岛素清除率降低。 mPer2的缺乏会导致Clock表达增加,Mkp1和Ide1的表达减少,这可能是观察到的表型的基础,这表明mPer2在循环胰岛素水平的调节中起作用。

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