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肠道中的T1r3和α-味导素调节胰高血糖素样肽-1的分泌。

T1r3 and alpha-gustducin in gut regulate secretion of glucagon-like peptide-1.

作者信息

Kokrashvili Zaza, Mosinger Bedrich, Margolskee Robert F

机构信息

Department of Neuroscience, Mount Sinai School of Medicine, New York, New York 10029, USA.

出版信息

Ann N Y Acad Sci. 2009 Jul;1170:91-4. doi: 10.1111/j.1749-6632.2009.04485.x.

Abstract

Glucagon-like peptide-1 (GLP-1) is an incretin hormone that underlies the augmented insulin release from the pancreas in response to glucose in the gut lumen more than to intravenous injected glucose (the "incretin effect"). GLP-1, found in enteroendocrine L cells of the gut, regulates appetite and gut motility and is released from L cells in response to glucose. GLP-1-expressing duodenal L cells also express T1r taste receptors, alpha-gustducin, and many other taste transduction elements. Knockout mice lacking alpha-gustducin or T1r3 have deficiencies in secretion of GLP-1 and in the regulation of plasma levels of insulin and glucose. Gut-expressed taste-signaling elements underlie multiple chemosensory functions of the gut including the incretin effect. Modulating hormone secretion from gut "taste cells" may provide novel treatments for obesity, diabetes, and malabsorption.

摘要

胰高血糖素样肽-1(GLP-1)是一种肠促胰岛素激素,它是肠道腔内葡萄糖比静脉注射葡萄糖更能促使胰腺增加胰岛素释放(即“肠促胰岛素效应”)的基础。GLP-1存在于肠道的肠内分泌L细胞中,调节食欲和肠道蠕动,并在对葡萄糖作出反应时从L细胞释放。表达GLP-1的十二指肠L细胞还表达味觉受体T1r、α-味导素以及许多其他味觉转导元件。缺乏α-味导素或T1r3的基因敲除小鼠在GLP-1分泌以及胰岛素和葡萄糖血浆水平调节方面存在缺陷。肠道表达的味觉信号元件是肠道多种化学感应功能(包括肠促胰岛素效应)的基础。调节肠道“味觉细胞”的激素分泌可能为肥胖症、糖尿病和吸收不良提供新的治疗方法。

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