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Gut-expressed gustducin and taste receptors regulate secretion of glucagon-like peptide-1

机译:肠表达的gustducin和味觉受体调节胰高血糖素样肽1的分泌

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摘要

Glucagon-like peptide-1 (GLP-1), released from gut endocrine L cells in response to glucose, regulates appetite, insulin secretion, and gut motility. How glucose given orally, but not systemically, induces GLP-1 secretion is unknown. We show that human duodenal L cells express sweet taste receptors, the taste G protein gustducin, and several other taste transduction elements. Mouse intestinal L cells also express α-gustducin. Ingestion of glucose by α-gustducin null mice revealed deficiencies in secretion of GLP-1 and the regulation of plasma insulin and glucose. Isolated small bowel and intestinal villi from α-gustducin null mice showed markedly defective GLP-1 secretion in response to glucose. The human L cell line NCI-H716 expresses a-gustducin, taste receptors, and several other taste signaling elements. GLP-1 release from NCI-H716 cells was promoted by sugars and the noncaloric sweetener sucralose, and blocked by the sweet receptor antagonist lactisole or siRNA for a-gustducin. We conclude that L cells of the gut "taste" glucose through the same mechanisms used by taste cells of the tongue. Modulating GLP-1 secretion in gut "taste cells" may provide an important treatment for obesity, diabetes and abnormal gut motility.
机译:胰高血糖素样肽1(GLP-1)响应于葡萄糖从肠内分泌L细胞释放,调节食欲,胰岛素分泌和肠蠕动。口服葡萄糖而不是全身性葡萄糖如何诱导GLP-1分泌尚不清楚。我们显示人十二指肠L细胞表达甜味受体,味G蛋白gustducin和其他几种味转导元件。小鼠肠道L细胞也表达α-gustducin。 α-gustducinnull小鼠摄入葡萄糖后发现GLP-1分泌不足以及血浆胰岛素和葡萄糖的调节不足。从α-gustducin缺失小鼠中分离出的小肠和肠绒毛对葡萄糖的反应显示出明显的GLP-1分泌缺陷。人L细胞系NCI-H716表达α-gustducin,味觉受体和其他几种味觉信号元件。糖和非热量甜味剂三氯蔗糖可促进NCI-H716细胞释放GLP-1,而甜味受体拮抗剂乳糖苷或siRNA可阻断a-gustducin。我们得出结论,肠道的L细胞通过舌味细胞所使用的相同机制来“品尝”葡萄糖。调节肠道“味觉细胞”中GLP-1的分泌可能为肥胖,糖尿病和异常肠道运动提供重要的治疗方法。

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