Journal Article

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

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

2017

Overview

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.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Animals / Antidiabetics / Beta cells / Binding sites / Biology and Life Sciences / Biomarkers / Body weight / Cell Line / CHO Cells / Cricetulus / Diabetes / Diabetes mellitus / Fatty acids / Glucagon / Glucagon - metabolism / Glucose / Glucose - metabolism / Glucose Tolerance Test / Humans / Incretins - metabolism / Inhibitor drugs / Insulin / Insulin - metabolism / Insulin Secretion / Islets of Langerhans - metabolism / Male / Medicine and Health Sciences / Metabolic disorders / Mice / Pancreas / Pharmaceutical sciences / Pharmacology / Physical Sciences / Rats / Receptors, G-Protein-Coupled - agonists / Rodents / Secretion / Secretions