Suppr超能文献

神经递质和肽对大鼠回肠胰高血糖素样肽-1分泌的调节

Regulation of glucagon-like peptide-1 secretion from rat ileum by neurotransmitters and peptides.

作者信息

Herrmann-Rinke C, Vöge A, Hess M, Göke B

机构信息

Department of Internal Medicine, Philipps University of Marburg, Germany.

出版信息

J Endocrinol. 1995 Oct;147(1):25-31. doi: 10.1677/joe.0.1470025.

Abstract

Food ingestion induces a rapid increase in the insulinotropic glucagon-like peptide-1 (GLP-1) in plasma. Paradoxically, GLP-1 originates from the lower intestines and therefore a complex regulation of postprandial GLP-1 secretion must exist. This was addressed in the present study by utilizing an isolated vascularly perfused rat ileum preparation. Peptides and neurotransmitters thought to be candidate mediators triggering GLP-1 secretion were arterially infused and GLP-1 was measured in the venous effluent. Arterial infusion of cholinergic agonists strongly enhanced GLP-1 secretion which was counteracted by the addition of atropine. Histamine, dopamine, 5-hydoxytryptamine, gamma-aminobutyric acid, and norepinephrine had no effect. Peptides of the bombesin family were strong stimulants whereas tachykinins, enkephalins, dynorphin, TRH, calcitonin-gene-related peptide and members of the secretin family, vasoactive intestinal peptide, peptide histidine isoleucine and neuropeptide Y, were less effective. The second incretin hormone, gastric inhibitory polypeptide (GIP), was the most potent stimulant of GLP-1 secretion in our study. It enhanced GLP-1 release up to sixfold above basal during the early phase followed by a sustained secretion at 400% above basal. This stimulation remained unaffected by atropine. In conclusion, in addition to luminal stimulation of nutrients, a cholinergic impulse as well as peptidergic mediators (among them possibly GIP and GRP) may have an impact on postprandial GLP-1 secretion from the rat ileum.

摘要

食物摄入会导致血浆中促胰岛素的胰高血糖素样肽-1(GLP-1)迅速增加。矛盾的是,GLP-1起源于下肠道,因此必然存在对餐后GLP-1分泌的复杂调节。本研究通过使用离体血管灌注大鼠回肠制剂来探讨这一问题。将被认为是触发GLP-1分泌的候选介质的肽和神经递质经动脉注入,并在静脉流出物中测量GLP-1。动脉注入胆碱能激动剂可强烈增强GLP-1分泌,而加入阿托品可抵消这种增强作用。组胺、多巴胺、5-羟色胺、γ-氨基丁酸和去甲肾上腺素无作用。蛙皮素家族的肽是强烈的刺激物,而速激肽、脑啡肽、强啡肽、促甲状腺激素释放激素、降钙素基因相关肽以及促胰液素家族的成员,如血管活性肠肽、肽组氨酸异亮氨酸和神经肽Y,作用较弱。在我们的研究中,第二种肠促胰岛素激素,即胃抑制多肽(GIP),是GLP-1分泌最有效的刺激物。在早期阶段,它可使GLP-1释放增强至基础水平的六倍以上,随后以高于基础水平400%的水平持续分泌。这种刺激不受阿托品影响。总之,除了腔内营养物质的刺激外,胆碱能冲动以及肽能介质(其中可能包括GIP和GRP)可能对大鼠回肠餐后GLP-1分泌有影响。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验