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胰高血糖素样肽 1 对食欲和体重的影响:重点关注中枢神经系统。

Effects of glucagon-like peptide 1 on appetite and body weight: focus on the CNS.

机构信息

Diabetes Centre, VU University Medical Centre, PO Box 7057, 1007 MB Amsterdam, The Netherlands Department of Endocrinology and Metabolism, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

J Endocrinol. 2014 Mar 7;221(1):T1-16. doi: 10.1530/JOE-13-0414. Print 2014 Apr.

Abstract

The delivery of nutrients to the gastrointestinal tract after food ingestion activates the secretion of several gut-derived mediators, including the incretin hormone glucagon-like peptide 1 (GLP-1). GLP-1 receptor agonists (GLP-1RA), such as exenatide and liraglutide, are currently employed successfully in the treatment of patients with type 2 diabetes mellitus. GLP-1RA improve glycaemic control and stimulate satiety, leading to reductions in food intake and body weight. Besides gastric distension and peripheral vagal nerve activation, GLP-1RA induce satiety by influencing brain regions involved in the regulation of feeding, and several routes of action have been proposed. This review summarises the evidence for a physiological role of GLP-1 in the central regulation of feeding behaviour and the different routes of action involved. Also, we provide an overview of presently available data on pharmacological stimulation of GLP-1 pathways leading to alterations in CNS activity, reductions in food intake and weight loss.

摘要

进食后,营养物质被输送到胃肠道,这会激活几种肠道来源的介质的分泌,包括肠促胰岛素激素胰高血糖素样肽 1(GLP-1)。GLP-1 受体激动剂(GLP-1RA),如 exenatide 和 liraglutide,目前被成功用于治疗 2 型糖尿病患者。GLP-1RA 可改善血糖控制并刺激饱腹感,从而减少食物摄入和体重。除了胃扩张和外周迷走神经激活外,GLP-1RA 通过影响参与进食调节的大脑区域来引起饱腹感,并且已经提出了几种作用途径。这篇综述总结了 GLP-1 在中枢调节进食行为中的生理作用以及涉及的不同作用途径的证据。此外,我们还概述了目前关于 GLP-1 途径的药理学刺激导致中枢神经系统活动改变、食物摄入减少和体重减轻的现有数据。

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