游离脂肪酸受体1
血糖性
兴奋剂
2型糖尿病
医学
内分泌学
内科学
化学
体内
逮捕
体外
胰岛素
药理学
糖尿病
受体
生物化学
生物
G蛋白偶联受体
生物技术
作者
Jongmin Yoon,Don‐Gil Lee,H. J. Song,Dahae Hong,Ji Soo Park,Chang‐Hee Hong,Kyung Mi An,Jungwoo Lee,Joon-Tae Park,Hongchul Yoon,Jihoon Tak,Sang Geon Kim
标识
DOI:10.1016/j.biopha.2024.117044
摘要
Xelaglifam, developed as a GPR40/FFAR1 agonist, induces glucose-dependent insulin secretion and reduces circulating glucose levels for Type 2 diabetes treatment. This study investigated the effects of Xelaglifam in comparison with Fasiglifam on the in vitro/in vivo anti-diabetic efficacy and selectivity, and the mechanistic basis. In vitro studies on downstream targets of Xelaglifam were performed in GPR40-expressing cells. Xelaglifam treatment exhibited dose-dependent effects, increasing inositol phosphate-1, Ca
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