生长素
普吕卡贡
PI3K/AKT/mTOR通路
内科学
内分泌学
产矿性
胰高血糖素样肽-1
化学
信号转导
生物
受体
激素
细胞生物学
神经肽Y受体
2型糖尿病
医学
糖尿病
神经肽
作者
Geyang Xu,Xiaosi Hong,Hong Tang,Sushi Jiang,Fenting Liu,Zhemin Shen,Ziru Li,Weizhen Zhang
标识
DOI:10.1016/j.mce.2015.08.016
摘要
Glucagon-like peptide (GLP-1), an intestinal incretin produced in L-cells and released in response to meal intake, functions to promote insulin secretion and to decrease plasma glucose. Ghrelin is an orexigenic hormone critical for glucose homeostasis. The molecular mechanism by which ghrelin alters GLP-1 production remains largely unknown. Here we showed that ghrelin attenuates GLP-1 production through mTOR signaling. In GHSR1a null mice, ileal mTOR signaling, proglucagon and circulating GLP-1 were significantly increased. Antagonism of the GHSR1a by D-Lys-3-GHRP-6 increased GLP-1 synthesis and release in STC-1 cells. Treatment of STC-1 cells with ghrelin decreased the production of GLP-1. This effect was associated with a significant inhibition of mTOR signaling. Overexpression of ghrelin inhibited proglucagon promoter activity and GLP-1 production. Inhibition of mTOR activity by mTOR siRNA blocked D-Lys-3-GHRP-6 induced GLP-1 production in STC-1 cells. Our results suggest that mTOR signaling mediates the inhibitory effect of ghrelin on GLP-1 production.
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