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肠促胰岛素激素:从科学发现到实际治疗。

The incretin hormones: from scientific discovery to practical therapeutics.

机构信息

VA San Diego Healthcare System and Center for Metabolic Research, 3350 La Jolla Village Drive, Mail Code 111G, San Diego, CA 92161, USA.

出版信息

Diabetologia. 2012 Jul;55(7):1865-8. doi: 10.1007/s00125-012-2561-x. Epub 2012 May 4.

Abstract

The incretins are gut hormones secreted in response to nutrient/carbohydrate ingestion and act on the pancreatic beta cell to amplify glucose-stimulated insulin secretion. Incretin hormone-based treatments for patients with type 2 diabetes represent a major advance in diabetes therapeutics. The ability of the incretin agents (glucagon-like peptide 1 [GLP-1] agonists and dipeptidyl peptidase IV [DPP-4] inhibitors) to improve glycaemia with a low associated risk of hypoglycaemia, together with beneficial/neutral effects on body weight, offers a significant advantage for both patients and treating clinicians. In this edition of 'Then and Now,' it is useful to look back 25 years and reflect upon the developments in this field since Nauck and colleagues published two seminal papers. In 1986 they first documented a reduced incretin effect in patients with type 2 diabetes (Diabetologia 29:46-52), and then in 1993 they demonstrated that, in patients with poorly controlled type 2 diabetes, a single exogenous infusion of an incretin (GLP-1) increased insulin levels in a glucose-dependent manner and normalised fasting hyperglycaemia (Diabetologia 36:741-744). In the ensuing 26 years, progress in the field of incretin hormones has resulted in a greater understanding of the relative roles of GLP-1 and glucose-dependent insulinotropic polypeptide secretion and activity in the pathogenesis of type 2 diabetes and the important recognition that native GLP-1 is quickly degraded by the ubiquitous protease DPP-4. This has led to the development of GLP-1 agonists that are resistant to degradation by DPP-4 and of selective inhibitors of DPP-4 activity as therapeutic agents. GLP-1 agonists (exenatide and liraglutide) and DPP-4 inhibitors (sitagliptin, vildagliptin, saxagliptin and linagliptin) currently represent effective treatment options for patients with type 2 diabetes. Several additional agents are in the pipeline, including longer acting DPP-4-resistant GLP-1 agonists. More exciting, however, is the increasing recognition that the incretin agents have numerous extra-glycaemic effects that could translate into potential cardiovascular and other benefits.

摘要

肠促胰岛素是响应营养/碳水化合物摄入而分泌的肠道激素,作用于胰岛β细胞以放大葡萄糖刺激的胰岛素分泌。基于肠促胰岛素激素的治疗方法代表了糖尿病治疗学的重大进展。肠促胰岛素制剂(胰高血糖素样肽 1 [GLP-1] 激动剂和二肽基肽酶 4 [DPP-4] 抑制剂)改善血糖的能力与低血糖相关风险低相关,同时对体重产生有益/中性影响,为患者和治疗临床医生都带来了显著优势。在这个“过去与现在”的版本中,回顾 25 年前,反思自 Nauck 及其同事发表两篇开创性论文以来该领域的发展是很有用的。1986 年,他们首次记录了 2 型糖尿病患者的肠促胰岛素效应降低(糖尿病学 29:46-52),然后在 1993 年,他们证明在控制不佳的 2 型糖尿病患者中,单次外源性输注肠促胰岛素(GLP-1)以葡萄糖依赖性方式增加胰岛素水平并使空腹高血糖正常化(糖尿病学 36:741-744)。在随后的 26 年中,肠促胰岛素激素领域的进展导致人们对 GLP-1 和葡萄糖依赖性胰岛素释放多肽分泌和活性在 2 型糖尿病发病机制中的相对作用有了更深入的了解,并重要地认识到天然 GLP-1 很快被无处不在的蛋白酶 DPP-4 降解。这导致了 GLP-1 激动剂的开发,这些激动剂对 DPP-4 的降解具有抗性,以及 DPP-4 活性的选择性抑制剂作为治疗剂。GLP-1 激动剂(艾塞那肽和利拉鲁肽)和 DPP-4 抑制剂(西格列汀、维格列汀、沙格列汀和利格列汀)目前是 2 型糖尿病患者的有效治疗选择。还有几种其他药物正在研发中,包括作用时间更长的 DPP-4 抗性 GLP-1 激动剂。然而,更令人兴奋的是,人们越来越认识到肠促胰岛素制剂具有许多额外的血糖作用,这可能转化为潜在的心血管和其他益处。

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