Mechanisms by which insulin, associated or not with glucose, may inhibit hepatic glucose production in the rat.

L Guignot, G Mithieux
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引用次数: 57

Abstract

We investigated the intrahepatic mechanisms by which insulin, associated or not with hyperglycemia, may inhibit hepatic glucose production (HGP) in the rat. After a hyperinsulinemic euglycemic clamp in postabsorptive (PA) anesthetized rats, the 70% inhibition of HGP could be explained by a dramatic decrease in the glucose 6-phosphate (G-6-P) concentration, whereas the glucose-6-phosphatase (G-6-Pase) and glucokinase (GK) activities were unchanged. Under hyperinsulinemic hyperglycemic condition, the GK flux was increased. The G-6-P concentration was not or only weakly decreased. The inhibition of HGP involved a significant 25% inhibition of the G-6-Pase activity. Under similar conditions in fasted rats, the GK flux was very low. The suppression of G-6-Pase and HGP did not occur, despite plasma insulin and glucose concentrations similar to those in PA rats. Therefore, 1) insulin suppresses HGP in euglycemia by solely decreasing the G-6-P concentration; 2) when combining both hyperinsulinemia and hyperglycemia, the suppression of HGP involves the inhibition of the G-6-Pase activity; and 3) a sustained glucose-phosphorylation flux might be a crucial determinant in the inhibition of G-6-Pase and of HGP.

胰岛素(与葡萄糖相关或不相关)抑制大鼠肝脏葡萄糖生成的机制。
我们研究了胰岛素在肝内抑制大鼠肝脏葡萄糖生成(HGP)的机制,无论是否与高血糖有关。在吸收后(PA)麻醉大鼠高胰岛素正糖钳夹后,HGP抑制70%可能是由于葡萄糖-6-磷酸(G-6-P)浓度急剧下降,而葡萄糖-6-磷酸酶(G-6-Pase)和葡萄糖激酶(GK)活性不变。在高胰岛素型高血糖状态下,GK通量增加。G-6-P浓度没有或只有微弱下降。对HGP的抑制作用包括对G-6-Pase活性的25%的显著抑制。在类似的条件下,禁食大鼠的GK通量非常低。尽管血浆胰岛素和葡萄糖浓度与PA大鼠相似,但G-6-Pase和HGP并未受到抑制。因此,1)胰岛素仅通过降低G-6-P浓度来抑制高血糖期的HGP;2)当合并高胰岛素血症和高血糖时,抑制HGP涉及抑制G-6-Pase活性;3)持续的葡萄糖磷酸化通量可能是抑制G-6-Pase和HGP的关键决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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