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胰岛素对恒河猴肝脏糖原合酶和糖原磷酸化酶的活性起相互调节作用。

Insulin regulates liver glycogen synthase and glycogen phosphorylase activity reciprocally in rhesus monkeys.

作者信息

Ortmeyer H K, Bodkin N L, Hansen B C

机构信息

Department of Physiology, School of Medicine, University of Maryland at Baltimore 21201, USA.

出版信息

Am J Physiol. 1997 Jan;272(1 Pt 1):E133-8. doi: 10.1152/ajpendo.1997.272.1.E133.

Abstract

In skeletal muscle of both humans and monkeys, the effects of in vivo insulin during a euglycemic hyperinsulinemic clamp on the enzymes and substrates of glycogen metabolism have been well established. In liver, such effects of insulin during a clamp have not been previously studied in primates. To examine insulin action at the liver, euglycemic hyperinsulinemic clamps were performed in 10 lean young adult male rhesus monkeys. Liver biopsies were obtained at three time points: basal (fasting), that is, immediately before the onset of the clamp, and during insulin infusion at 130 and 195 min. Glycogen synthase (GS), glycogen phosphorylase (GP), glucose 6-phosphate (G-6-P), and glycogen were determined at each time point, with the greatest effects observed most frequently at 195 min. Whole body insulin-mediated glucose disposal rate was related to the change in the independent activity of GS (r = 0.63, P < 0.05). Insulin increased the GS fractional activity (P < 0.005) and decreased the activity ratio of GP (P < 0.001) compared with basal. The changes in fractional activity of GS and in activity ratio of GP were inversely related (r = - 0.68, P < 0.05), G-6-P concentration was decreased during insulin stimulation compared with basal (P = 0.01). Glycogen concentration was not significantly different between the basal and insulin-stimulated time points. We conclude that insulin during a euglycemic clamp activates liver GS while inhibiting liver GP and that insulin action on liver GS is positively related to whole body insulin-mediated glucose disposal rates in lean young adult rhesus monkeys.

摘要

在人类和猴子的骨骼肌中,正常血糖高胰岛素钳夹期间体内胰岛素对糖原代谢的酶和底物的影响已得到充分证实。在肝脏中,此前尚未在灵长类动物中研究过钳夹期间胰岛素的此类作用。为了研究胰岛素在肝脏中的作用,对10只瘦的年轻成年雄性恒河猴进行了正常血糖高胰岛素钳夹。在三个时间点获取肝脏活检样本:基础值(空腹),即钳夹开始前即刻,以及在胰岛素输注130分钟和195分钟时。在每个时间点测定糖原合酶(GS)、糖原磷酸化酶(GP)、6-磷酸葡萄糖(G-6-P)和糖原,最常见的最大影响出现在195分钟时。全身胰岛素介导的葡萄糖处置率与GS独立活性的变化相关(r = 0.63,P < 0.05)。与基础值相比,胰岛素增加了GS分数活性(P < 0.005)并降低了GP的活性比(P < 0.001)。GS分数活性的变化与GP活性比的变化呈负相关(r = - 0.68,P < 0.05),与基础值相比,胰岛素刺激期间G-6-P浓度降低(P = 0.01)。基础值和胰岛素刺激时间点之间的糖原浓度无显著差异。我们得出结论,在正常血糖钳夹期间,胰岛素激活肝脏GS,同时抑制肝脏GP,并且胰岛素对肝脏GS的作用与瘦的年轻成年恒河猴全身胰岛素介导的葡萄糖处置率呈正相关。

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