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空腹高血糖会损害葡萄糖介导而非胰岛素介导的胰高血糖素分泌抑制作用。

Fasting hyperglycemia impairs glucose- but not insulin-mediated suppression of glucagon secretion.

作者信息

Abdul-Ghani Muhammad, DeFronzo Ralph A

机构信息

Diabetes Division, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX 78229, USA.

出版信息

J Clin Endocrinol Metab. 2007 May;92(5):1778-84. doi: 10.1210/jc.2006-1515. Epub 2007 Feb 27.

Abstract

AIM

Our aim was to assess the effect of chronic hyperglycemia on glucose- and insulin-mediated suppression of glucagon secretion by the alpha-cell.

METHODS

Thirty subjects with normal glucose tolerance, 27 with impaired fasting glucose and/or impaired glucose tolerance, and 32 type 2 diabetic subjects were studied with oral glucose tolerance test (OGTT) and euglycemic hyperinsulinemic clamp. Fasting plasma glucagon concentration and plasma glucagon concentration during the OGTT and insulin clamp were measured.

RESULTS

During the OGTT, the decrement in the plasma glucagon concentration (area under the curve) was correlated inversely with the fasting plasma glucose concentration (r = -0.35; P < 0.001). As the fasting glucose level increased, the suppression of plasma glucagon progressively diminished. In contrast, during the euglycemic insulin clamp, the suppression of plasma glucagon was not correlated with the fasting plasma glucose concentration and was similar in subjects with normal glucose tolerance, subjects with impaired fasting glucose/impaired glucose tolerance, and diabetic subjects: 18, 23, and 18%, respectively.

CONCLUSION

Insulin-mediated suppression of glucagon secretion is unrelated to the fasting plasma glucose concentration and is not impaired by chronic hyperglycemia. Thus, the defect in plasma glucagon suppression during the OGTT most likely results from impaired glucose-mediated glucagon suppression. The close correlation between fasting plasma glucose concentration and reduced glucagon suppression suggests a glucotoxic effect on alpha-cell function.

摘要

目的

我们的目的是评估慢性高血糖对α细胞葡萄糖和胰岛素介导的胰高血糖素分泌抑制作用的影响。

方法

对30名糖耐量正常的受试者、27名空腹血糖受损和/或糖耐量受损的受试者以及32名2型糖尿病受试者进行口服葡萄糖耐量试验(OGTT)和正常血糖高胰岛素钳夹试验研究。测量空腹血浆胰高血糖素浓度以及OGTT和胰岛素钳夹试验期间的血浆胰高血糖素浓度。

结果

在OGTT期间,血浆胰高血糖素浓度的下降(曲线下面积)与空腹血浆葡萄糖浓度呈负相关(r = -0.35;P < 0.001)。随着空腹血糖水平升高,血浆胰高血糖素的抑制作用逐渐减弱。相比之下,在正常血糖胰岛素钳夹试验期间,血浆胰高血糖素的抑制作用与空腹血浆葡萄糖浓度无关,并且在糖耐量正常的受试者、空腹血糖受损/糖耐量受损的受试者和糖尿病受试者中相似,分别为18%、23%和18%。

结论

胰岛素介导的胰高血糖素分泌抑制与空腹血浆葡萄糖浓度无关,且不受慢性高血糖的损害。因此,OGTT期间血浆胰高血糖素抑制缺陷很可能是由葡萄糖介导的胰高血糖素抑制受损所致。空腹血浆葡萄糖浓度与胰高血糖素抑制减弱之间的密切相关性表明对α细胞功能存在糖毒性作用。

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