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二肽基肽酶-IV抑制剂在糖尿病患者中的治疗潜力

Therapeutic potential of dipeptidyl peptidase-IV inhibitors in patients with diabetes mellitus.

作者信息

Moore Kevin B, Saudek Christopher D

机构信息

Division of Endocrinology and Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

出版信息

Am J Ther. 2008 Sep-Oct;15(5):484-91. doi: 10.1097/MJT.0b013e3180ed42dc.

Abstract

Dipeptidyl peptidase-IV (DPP-IV) inhibitors are a new class of oral antidiabetic agents for the treatment of patients with type 2 diabetes. Inhibition of the enzyme DPP-IV results in increased activity of glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP), the incretin hormones. Through the action of GLP-1 and GIP, DPP-IV inhibitors improve preprandial and postprandial glucose by enhancing insulin secretion and reducing postprandial concentrations of glucagon. This review examines the background, current evidence, and future therapeutic potential of this novel class of drug.

摘要

二肽基肽酶-IV(DPP-IV)抑制剂是一类新型口服抗糖尿病药物,用于治疗2型糖尿病患者。抑制DPP-IV酶会导致肠促胰岛素激素胰高血糖素样肽-1(GLP-1)和葡萄糖依赖性促胰岛素多肽(GIP)的活性增加。通过GLP-1和GIP的作用,DPP-IV抑制剂通过增强胰岛素分泌和降低餐后胰高血糖素浓度来改善餐前和餐后血糖。本文综述了这类新型药物的背景、现有证据及未来的治疗潜力。

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