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二肽基肽酶-4 抑制剂与二甲双胍联合使用会使活性 GLP-1 的血浆浓度呈相加性增加。

Dipeptidyl peptidase-4 inhibitors administered in combination with metformin result in an additive increase in the plasma concentration of active GLP-1.

机构信息

Merck Research Laboratories, Rahway, New Jersey, USA.

出版信息

Clin Pharmacol Ther. 2010 Dec;88(6):801-8. doi: 10.1038/clpt.2010.184. Epub 2010 Nov 3.

Abstract

The aim of the study was to investigate the effects of a dipeptidyl peptidase-4 (DPP-4) inhibitor, of metformin, and of the combination of the two agents, on incretin hormone concentrations. Active and inactive (or total) incretin plasma concentrations, plasma DPP-4 activity, and preproglucagon (GCG) gene expression were determined after administration of each agent alone or in combination to mice with diet-induced obesity (DIO) and to healthy human subjects. In mice, metformin increased Gcg expression in the large intestine and elevated the plasma concentrations of inactive glucagon-like peptide 1 (GLP-1) (9-36) and glucagon. In healthy subjects, a DPP-4 inhibitor elevated both active GLP-1 and glucose dependent insulinotropic polypeptide (GIP), metformin increased total GLP-1 (but not GIP), and the combination resulted in additive increases in active GLP-1 plasma concentrations. Metformin did not inhibit plasma DPP-4 activity either in vitro or in vivo. The study results show that metformin is not a DPP-4 inhibitor but rather enhances precursor GCG expression in the large intestine, resulting in increased total GLP-1 concentrations. DPP-4 inhibitors and metformin have complementary mechanisms of action and additive effects with respect to increasing the concentrations of active GLP-1 in plasma.

摘要

这项研究的目的是探讨二肽基肽酶-4(DPP-4)抑制剂、二甲双胍以及这两种药物联合应用对肠降血糖素激素浓度的影响。在给予单独或联合使用这些药物后,测定了饮食诱导肥胖(DIO)的小鼠和健康人体的活性和非活性(或总)肠降血糖素的血浆浓度、血浆 DPP-4 活性和前胰高血糖素(GCG)基因表达。在小鼠中,二甲双胍增加了大肠中的 Gcg 表达,并升高了非活性胰高血糖素样肽 1(GLP-1)(9-36)和胰高血糖素的血浆浓度。在健康受试者中,DPP-4 抑制剂升高了活性 GLP-1 和葡萄糖依赖性胰岛素释放肽(GIP),二甲双胍增加了总 GLP-1(但不增加 GIP),联合使用导致活性 GLP-1 血浆浓度的相加增加。二甲双胍无论是在体外还是在体内都没有抑制血浆 DPP-4 活性。研究结果表明,二甲双胍不是 DPP-4 抑制剂,而是增强了大肠中的前体 GCG 表达,从而增加了总 GLP-1 浓度。DPP-4 抑制剂和二甲双胍在增加血浆中活性 GLP-1 浓度方面具有互补的作用机制和相加作用。

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