肠促胰岛素
2型糖尿病
葡萄糖稳态
医学
胰岛素
兴奋剂
糖尿病
药理学
激素
体内
艾塞那肽
内科学
胰岛素抵抗
受体
生物
内分泌学
生物技术
作者
Deanne H. Hryciw,Rhiannon K. Patten,Raymond J. Rodgers,Joseph Proietto,Dana S. Hutchinson,Andrew J. McAinch
标识
DOI:10.1080/13543784.2024.2321271
摘要
GPR119 agonists in vitro and in vivo can potentially regulate incretin hormone release from the gut, then pancreatic insulin release which regulates blood glucose concentrations. However, the success in controlling glucose homeostasis in rodent models of T2D and obesity, failed to translate to early-stage clinical trials in patients with T2D. However, in more recent studies, acute and chronic dosing with the GPR119 agonist DS-8500a had increased efficacy, although this compound was discontinued for further development. New trials on GPR119 agonists are needed, however it may be that the future of GPR119 agonists lie in the development of combination therapy with other T2D therapeutics.
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