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

Authors :
Michele J Pachanski
Melissa E Kirkland
Daniel T Kosinski
Joel Mane
Boonlert Cheewatrakoolpong
Jiyan Xue
Daphne Szeto
Gail Forrest
Corin Miller
Michelle Bunzel
Christopher W Plummer
Harry R Chobanian
Michael W Miller
Sarah Souza
Brande S Thomas-Fowlkes
Aimie M Ogawa
Adam B Weinglass
Jerry Di Salvo
Xiaoyan Li
Yue Feng
Daniel A Tatosian
Andrew D Howard
Steven L Colletti
Maria E Trujillo
Source :
PLoS ONE, Vol 12, Iss 10, p e0186033 (2017)
Publication Year :
2017
Publisher :
Public Library of Science (PLoS), 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.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
19326203
Volume :
12
Issue :
10
Database :
Directory of Open Access Journals
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
edsdoj.32189b3be78e4819b3311bc01c779ade
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pone.0186033