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Central leptin acutely reverses diet-induced hepatic insulin resistance.

机译:中央瘦素可迅速逆转饮食引起的肝胰岛素抵抗。

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Voluntary overfeeding rapidly induces resistance to the effects of systemic insulin and leptin on liver glucose metabolism. To examine whether central administration of recombinant leptin can restore leptin and insulin action on liver glucose fluxes, we infused leptin in the third cerebral ventricle of conscious overfed rats during pancreatic-insulin clamp studies. The effect of leptin on the phosphorylation of the signal transducer and activator of transcription-3 in the arcuate nuclei of the hypothalamus was similar in animals fed a regular diet or a high-fat diet for 3 days. The infusion of leptin in the third cerebral ventricle markedly inhibited glucose production in rats fed a high-fat diet mainly by decreasing glycogenolysis. The inhibition of glycogenolysis was sufficient to normalize glucose production and was accompanied by leptin-induced decreases in the hepatic expression of glucose-6-phosphatase and phosphoenolpyruvate carboxykinase. Thus central administration of leptin rescues the hepatic insulin resistance induced by short-term hyperphagia.
机译:自愿过量喂养会迅速引起对全身性胰岛素和瘦素对肝脏葡萄糖代谢影响的抗性。为了检查重组瘦素的中央给药是否可以恢复瘦素和胰岛素对肝葡萄糖通量的作用,我们在胰腺-胰岛素钳夹研究中将瘦素注入了有意识的饮食过量大鼠的第三脑室中。瘦素对下丘脑弓状核中信号转导和转录激活因子3磷酸化的影响在喂食普通饮食或高脂饮食3天的动物中相似。瘦素在第三脑室的输注显着抑制了高脂饮食喂养的大鼠体内的葡萄糖生成,主要是通过减少糖原分解作用。糖原分解的抑制足以使葡萄糖产生正常化,并伴有瘦素诱导的葡萄糖-6-磷酸酶和磷酸烯醇丙酮酸羧激酶的肝表达下降。因此,瘦素的中央给药可挽救短期食欲亢进引起的肝胰岛素抵抗。

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