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
逮捕
糖尿病
受体
G蛋白偶联受体
作者
Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon,Jongmin Yoon
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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