肠促胰岛素和DPP-4抑制剂治疗2型糖尿病的药物化学及应用

Q2 Pharmacology, Toxicology and Pharmaceutics
Open Medicinal Chemistry Journal Pub Date : 2011-01-01 Epub Date: 2011-09-09 DOI:10.2174/1874104501105010082
Mohamed Lotfy, Jaipaul Singh, Huba Kalász, Kornelia Tekes, Ernest Adeghate
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引用次数: 43

摘要

糖尿病(DM)是一种主要的代谢紊乱,目前影响着全球超过2亿人。大约90%的糖尿病患者患有2型糖尿病(T2DM)。全球经济每年要花费数十亿美元用于诊断、治疗和管理糖尿病患者。研究表明,天然存在的肠道激素肠促胰岛素、葡萄糖依赖性胰岛素性多肽(GIP)和胰高血糖素样肽-1 (GLP-1)可以维持胰腺β细胞的形态和功能。此外,GIP和GLP-1作用于胰岛素受体,促进胰岛素受体结合,使葡萄糖代谢达到最佳状态。本文综述了肠促胰岛素的药物化学和作用,特别是GLP-1和可以模仿其作用并防止其酶降解的药物。综述讨论了GLP-1激动剂,如艾塞那肽、利拉鲁肽、tasopoglutide和albiglutide。本文还鉴定和综述了一些抑制剂,它们可以阻断二肽基肽酶4 (DPP-4),该酶负责GLP-1的快速降解。这些DPP-4抑制剂包括西格列汀、沙格列汀、维格列汀和许多其他仍处于实验阶段的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Medicinal Chemistry and Applications of Incretins and DPP-4 Inhibitors in the Treatment of Type 2 Diabetes Mellitus.

Medicinal Chemistry and Applications of Incretins and DPP-4 Inhibitors in the Treatment of Type 2 Diabetes Mellitus.

Medicinal Chemistry and Applications of Incretins and DPP-4 Inhibitors in the Treatment of Type 2 Diabetes Mellitus.

Medicinal Chemistry and Applications of Incretins and DPP-4 Inhibitors in the Treatment of Type 2 Diabetes Mellitus.

Diabetes mellitus (DM) is a major metabolic disorder currently affecting over 200 million people worldwide. Approximately 90% of all diabetic patients suffer from Type 2 diabetes mellitus (T2DM). The world's economy coughs out billions of dollars annually to diagnose, treat and manage patients with diabetes. It has been shown that the naturally occurring gut hormones incretins, glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) can preserve the morphology and function of pancreatic beta cell. In addition, GIP and GLP-1 act on insulin receptors to facilitate insulin-receptor binding, resulting in optimal glucose metabolism. This review examines the medicinal chemistry and roles of incretins, specifically, GLP-1 and drugs which can mimic its actions and prevent its enzymatic degradation. The review discussed GLP-1 agonists such as exenatide, liraglutide, taspoglutide and albiglutide. The paper also identified and reviewed a number of inhibitors, which can block dipeptidyl peptidase 4 (DPP-4), the enzyme responsible for the rapid degradation of GLP-1. These DPP-4 inhibitors include sitagliptin, saxagliptin, vildagliptin and many others which are still in the experimental phase.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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