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高血糖本身(停用胰岛素和胰高血糖素)可抑制人体肝脏的葡萄糖生成。

Hyperglycemia per se (insulin and glucagon withdrawn) can inhibit hepatic glucose production in man.

作者信息

Liljenquist J E, Mueller G L, Cherrington A D, Perry J M, Rabinowitz D

出版信息

J Clin Endocrinol Metab. 1979 Jan;48(1):171-5. doi: 10.1210/jcem-48-1-171.

Abstract

We examined the effect of hyperglycemia per se on net splanchnic glucose balance. In 2 groups of normal postabsorptive men who had undergone hepatic vein catheterization, somatostatin was administered to block endogenous insulin and glucagon secretion. Exogenous glucose was infused in both groups to maintain euglycemia for 2 h in one group (n = 7) and to induce hyperglycemia of 220-240 mg/dl after 30 minutes of euglycemia in the second group (n = 4). In both groups the induction of insulinopenia and glucagonopenia with euglycemia maintained resulted in an initial 75% fall in net splanchnic glucose production (NSGP). In the group in which euglycemia was maintained NSGP returned to basal rates (157 +/- 31 mg/min) within 2 h. However, in the group in which hyperglycemia was induced, NSGP did not return to basal rates but remained suppressed (28 +/- 4 mg/min) for the duration of the study. These data in normal man indicate that hyperglycemia per se with insulin and glucagon acutely withdrawn can suppress splanchnic glucose production but does not induce net splanchnic glucose storage.

摘要

我们研究了高血糖本身对内脏葡萄糖净平衡的影响。在两组接受肝静脉插管的正常空腹男性中,给予生长抑素以阻断内源性胰岛素和胰高血糖素的分泌。两组均输注外源性葡萄糖,一组(n = 7)维持血糖正常2小时,另一组(n = 4)在血糖正常30分钟后诱导血糖升高至220 - 240 mg/dl。在两组中,维持血糖正常并诱导胰岛素缺乏和胰高血糖素缺乏导致内脏葡萄糖净生成(NSGP)最初下降75%。在维持血糖正常的组中,NSGP在2小时内恢复至基础水平(157±31 mg/min)。然而,在诱导高血糖的组中,NSGP未恢复至基础水平,而是在研究期间持续受到抑制(28±4 mg/min)。这些在正常男性中的数据表明,在胰岛素和胰高血糖素急性撤除的情况下,高血糖本身可抑制内脏葡萄糖生成,但不会诱导内脏葡萄糖净储存。

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