化学
兴奋剂
游离脂肪酸受体1
激素
部分激动剂
药效学
药代动力学
肠内分泌细胞
G蛋白偶联受体
药理学
内分泌学
内科学
生物化学
内分泌系统
受体
医学
作者
Christopher R. Moyes,Shuwen He,Simon Mathieu,S.L. Lehman,Macrina T. Francisco,Eyal Vardy,Giuseppe Terracina,Ani Galstian,Monika J. M. Murphy,Gregory Poterewicz,Daniel Kosinski,Xiaodong Yang,Shuqin Zheng,Bryan Chan,Matthew J. Consolati,Richard A. Tschirret-Guth,Michael R. Luzung,Robert Saklatvala,Gregory D. Rak,Robert P. J. Barretto
标识
DOI:10.1021/acs.jmedchem.5c01030
摘要
Bariatric surgery provides long-term and robust weight loss in most patients. One leading hypothesis for this profound efficacy focuses on the increased activation of gut enteroendocrine cells (EECs), resulting in enhanced secretion of satiety hormones. We describe herein an approach using a combination of gut-targeted small molecules to stimulate intestinal nutrient receptors and mirror some of the hormone effects of bariatric surgery. In preclinical studies, administration of GPR40 agonist K-757 in combination with GPR119 agonist K-833 resulted in robust increases in the level of circulating hormones. In initial clinical studies, pharmacokinetics and pharmacodynamics for each molecule were characterized and largely recapitulated the effects of the individual compounds in mice.
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