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Knockdown of Neuropeptide Y in the Dorsomedial Hypothalamus Promotes Hepatic Insulin Sensitivity in Male Rats

机译:敲除下丘脑下丘脑神经肽Y促进雄性大鼠肝胰岛素敏感性。

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Recent evidence has shown that alterations in dorsomedial hypothalamic (DMH) neuropeptide Y (NPY) signaling influence glucose homeostasis, but the mechanism through which DMH NPY acts to affect glucose homeostasis remains unclear. Here we report that DMH NPY descending signals to the dorsal motor nucleus of the vagus (DMV) modulate hepatic insulin sensitivity to control hepatic glucose production in rats. Using the hyperinsulinemic-euglycemic clamp, we revealed that knockdown of NPY in the DMH by adeno-associated virus-mediated NPY-specific RNAi promoted insulin's action on suppression of hepatic glucose production. This knockdown silenced DMH NPY descending signals to the DMV, leading to an elevation of hepatic vagal innervation. Hepatic vagotomy abolished the inhibitory effect of DMH NPY knockdown on hepatic glucose production, but this glycemic effect was not affected by vagal deafferentation. Together, these results demonstrate a distinct role for DMHNPY in the regulation of glucose homeostasis through the hepatic vagal efferents and insulin action on hepatic glucose production.
机译:最近的证据表明,背部丘脑下丘脑(DMH)神经肽Y(NPY)信号的改变会影响葡萄糖稳态,但DMH NPY通过其影响葡萄糖稳态的机制尚不清楚。在这里我们报告到迷走神经(DMV)的背运动核DMH NPY下降信号调节肝胰岛素敏感性,以控制大鼠肝葡萄糖的产生。使用高胰岛素-正常血糖钳夹,我们揭示了腺相关病毒介导的NPY特异性RNAi抑制DMH中NPY的表达促进了胰岛素抑制肝葡萄糖生成的作用。这种击倒使DMH NPY下降到DMV的信号沉默,导致肝迷走神经支配性升高。肝迷走神经切断术取消了DMH NPY敲低对肝葡萄糖生成的抑制作用,但这种血糖作用不受迷走神经脱除咖啡因的影响。在一起,这些结果表明DMHNPY在通过肝迷走神经传出和胰岛素对肝葡萄糖生成的作用来调节葡萄糖稳态中的独特作用。

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