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首页> 外文期刊>Archives of physiology and biochemistry >Dynamics of insulin signalling in liver during hyperinsulinemic euglycaemic clamp conditions in vivo and the effects of high-fat feeding in male mice.
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Dynamics of insulin signalling in liver during hyperinsulinemic euglycaemic clamp conditions in vivo and the effects of high-fat feeding in male mice.

机译:高胰岛素正常血糖钳制条件下体内肝脏中胰岛素信号的动态变化以及高脂喂养对雄性小鼠的影响。

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摘要

Insulin is an important regulator of hepatic carbohydrate, lipid, and protein metabolism, and the regulation of these processes by insulin is disturbed under conditions of insulin resistance and type 2 diabetes. Despite these alterations, the impact of insulin resistance on insulin signalling in the liver is not well defined. Variations in time and dose of insulin stimulation as well as plasma glucose levels may underlie this. The present study aimed at determining the dynamics of activation of hepatic insulin signalling in vivo at insulin concentrations resembling those achieved after a meal, and addressing the effects of high-fat feeding. An unexpected finding of this study was the biphasic activation pattern of the IRS-PI3K-PKB/Akt pathway. Our findings indicate that the first burst of activation contributes to regulation of glucose metabolism. The physiological function of the second peak is still unknown, but may involve regulation of protein synthesis. Finally, high-fat feeding caused hepatic insulin resistance, as illustrated by a reduced suppression of hepatic glucose production. A sustained increased phosphorylation of the serine/threonine kinases p70S6kinase and Jun N-terminal kinase in the absence of insulin may underlie the abrogated phosphorylation of the IRS proteins and their downstream targets.
机译:胰岛素是肝脏碳水化合物,脂质和蛋白质代谢的重要调节剂,在胰岛素抵抗和2型糖尿病的情况下,胰岛素对这些过程的调节受到干扰。尽管有这些改变,但胰岛素抵抗对肝脏中胰岛素信号的影响尚不明确。胰岛素刺激的时间和剂量以及血浆葡萄糖水平的变化可能是其基础。本研究旨在确定与餐后达到的胰岛素浓度相似的体内肝脏胰岛素信号激活的动力学,并探讨高脂喂养的影响。这项研究的意外发现是IRS-PI3K-PKB / Akt通路的双相激活模式。我们的发现表明,激活的首发有助于葡萄糖代谢的调节。第二个峰的生理功能仍然未知,但可能涉及蛋白质合成的调节。最后,高脂喂养引起肝胰岛素抵抗,如减少的肝葡萄糖生成抑制作用所说明。在没有胰岛素的情况下,丝氨酸/苏氨酸激酶p70S6激酶和Jun N末端激酶的持续磷酸化可能是IRS蛋白及其下游靶点被废除的磷酸化的基础。

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