Suppr超能文献

GPR40部分激动剂和正向变构调节剂:对啮齿动物葡萄糖和激素分泌的不同影响

GPR40 partial agonists and AgoPAMs: Differentiating effects on glucose and hormonal secretions in the rodent.

作者信息

Pachanski Michele J, Kirkland Melissa E, Kosinski Daniel T, Mane Joel, Cheewatrakoolpong Boonlert, Xue Jiyan, Szeto Daphne, Forrest Gail, Miller Corin, Bunzel Michelle, Plummer Christopher W, Chobanian Harry R, Miller Michael W, Souza Sarah, Thomas-Fowlkes Brande S, Ogawa Aimie M, Weinglass Adam B, Di Salvo Jerry, Li Xiaoyan, Feng Yue, Tatosian Daniel A, Howard Andrew D, Colletti Steven L, Trujillo Maria E

机构信息

In Vivo Pharmacology, Merck & Co., Inc., Kenilworth, New Jersey, United States of America.

Translational Imaging Biomarkers, Merck & Co., Inc., Kenilworth, New Jersey, United States of America.

出版信息

PLoS One. 2017 Oct 20;12(10):e0186033. doi: 10.1371/journal.pone.0186033. eCollection 2017.

Abstract

GPR40 agonists are effective antidiabetic agents believed to lower glucose through direct effects on the beta cell to increase glucose stimulated insulin secretion. However, not all GPR40 agonists are the same. Partial agonists lower glucose through direct effects on the pancreas, whereas GPR40 AgoPAMs may incorporate additional therapeutic effects through increases in insulinotrophic incretins secreted by the gut. Here we describe how GPR40 AgoPAMs stimulate both insulin and incretin secretion in vivo over time in diabetic GK rats. We also describe effects of AgoPAMs in vivo to lower glucose and body weight beyond what is seen with partial GPR40 agonists in both the acute and chronic setting. Further comparisons of the glucose lowering profile of AgoPAMs suggest these compounds may possess greater glucose control even in the presence of elevated glucagon secretion, an unexpected feature observed with both acute and chronic treatment with AgoPAMs. Together these studies highlight the complexity of GPR40 pharmacology and the potential additional benefits AgoPAMs may possess above partial agonists for the diabetic patient.

摘要

GPR40激动剂是有效的抗糖尿病药物,据信可通过直接作用于β细胞来降低血糖,从而增加葡萄糖刺激的胰岛素分泌。然而,并非所有GPR40激动剂都是一样的。部分激动剂通过直接作用于胰腺来降低血糖,而GPR40 AgoPAMs可能通过增加肠道分泌的促胰岛素分泌的肠促胰岛素而具有额外的治疗效果。在此,我们描述了GPR40 AgoPAMs如何在糖尿病GK大鼠体内随时间刺激胰岛素和肠促胰岛素的分泌。我们还描述了AgoPAMs在体内降低血糖和体重的效果,这超出了部分GPR40激动剂在急性和慢性情况下的作用。对AgoPAMs降血糖情况的进一步比较表明,即使在胰高血糖素分泌升高的情况下,这些化合物仍可能具有更好的血糖控制效果,这是AgoPAMs急性和慢性治疗中观察到的一个意外特征。这些研究共同强调了GPR40药理学的复杂性以及AgoPAMs相对于部分激动剂可能为糖尿病患者带来的潜在额外益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ade2/5650142/4f1724928240/pone.0186033.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验