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胰高血糖素在正常人体内肝葡萄糖生成调节中起重要作用的证据。

Evidence for an important role of glucagon in the regulation of hepatic glucose production in normal man.

作者信息

Liljenquist J E, Mueller G L, Cherrington A D, Keller U, Perry J M, Lacy W W, Rabinowitz D

出版信息

J Clin Invest. 1977 Feb;59(2):369-74. doi: 10.1172/JCI108649.

Abstract

To investigate the role of glucagon in regulating hepatic glucose production in man, selective glucagon deficiency was produced in four normal men by infusing somatostatin (0.9 mg/h) and regular pork insulin (150-muU/kg per min) for 2 h. Exogenous glucose was infused to maintain euglycemia. Arterial plasma glucagon levels fell by greater than 50% whereas plasma insulin levels were maintained in the range of 10-14 muU/ml. In response to these hormonal changes, net splanchnic glucose production (NSGP) fell by 75% and remained suppressed for the duration of the study. In contrast, when somatostatin alone was administered to normal men, resulting in combined insulin and glucagon deficiency (euglycemia again maintained), NSGP fell markedly but only transiently, reaching its nadir at 15 min. Thereafter, NSGP rose progressively, reaching the basal rate at 105 min. These data indicate that the induction of selective glucagon deficiency in man (with basal insulin levels maintained) is associated with a marked and sustained fall in hepatic glucose production. We conclude, therefore, that basal glucagon plays an important role in the maintenance of basal hepatic glucose production in normal man.

摘要

为了研究胰高血糖素在调节人体肝脏葡萄糖生成中的作用,对4名正常男性输注生长抑素(0.9毫克/小时)和正规猪胰岛素(150微单位/千克每分钟)2小时,造成选择性胰高血糖素缺乏。输注外源性葡萄糖以维持血糖正常。动脉血浆胰高血糖素水平下降超过50%,而血浆胰岛素水平维持在10 - 14微单位/毫升范围内。针对这些激素变化,内脏葡萄糖净生成量(NSGP)下降了75%,并在研究期间持续受到抑制。相比之下,当仅对正常男性给予生长抑素,导致胰岛素和胰高血糖素联合缺乏(同样维持血糖正常)时,NSGP显著下降,但只是短暂的,在15分钟时降至最低点。此后,NSGP逐渐上升,在105分钟时达到基础速率。这些数据表明,在人体中诱导选择性胰高血糖素缺乏(维持基础胰岛素水平)与肝脏葡萄糖生成的显著且持续下降有关。因此,我们得出结论,基础胰高血糖素在维持正常人体基础肝脏葡萄糖生成中起重要作用。

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