Document Detail


GPR119 regulates murine glucose homeostasis through incretin receptor-dependent and independent mechanisms.
MedLine Citation:
PMID:  21068156     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
G protein-coupled receptor 119 (GPR119) was originally identified as a β-cell receptor. However, GPR119 activation also promotes incretin secretion and enhances peptide YY action. We examined whether GPR119-dependent control of glucose homeostasis requires preservation of peptidergic pathways in vivo. Insulin secretion was assessed directly in islets, and glucoregulation was examined in wild-type (WT), single incretin receptor (IR) and dual IR knockout (DIRKO) mice. Experimental endpoints included plasma glucose, insulin, glucagon, glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic peptide (GIP), and peptide YY. Gastric emptying was assessed in WT, Glp1r-/-, DIRKO, Glp2r-/-, and GPR119-/- mice treated with the GPR119 agonist AR231453. AR231453 stimulated insulin secretion from WT and DIRKO islets in a glucose-dependent manner, improved glucose homeostasis, and augmented plasma levels of GLP-1, GIP, and insulin in WT and Gipr-/- mice. In contrast, although AR231453 increased levels of GLP-1, GIP, and insulin, it failed to lower glucose in Glp1r-/- and DIRKO mice. Furthermore, AR231453 did not improve ip glucose tolerance and had no effect on insulin action in WT and DIRKO mice. Acute GPR119 activation with AR231453 inhibited gastric emptying in Glp1r-/-, DIRKO, Glp2r-/-, and in WT mice independent of the Y2 receptor (Y2R); however, AR231453 did not control gastric emptying in GPR119-/- mice. Our findings demonstrate that GPR119 activation directly stimulates insulin secretion from islets in vitro, yet requires intact IR signaling and enteral glucose exposure for optimal control of glucose tolerance in vivo. In contrast, AR231453 inhibits gastric emptying independent of incretin, Y2R, or Glp2 receptors through GPR119-dependent pathways. Hence, GPR119 engages multiple complementary pathways for control of glucose homeostasis.
Authors:
Grace Flock; Dianne Holland; Yutaka Seino; Daniel J Drucker
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-11-10
Journal Detail:
Title:  Endocrinology     Volume:  152     ISSN:  1945-7170     ISO Abbreviation:  Endocrinology     Publication Date:  2011 Feb 
Date Detail:
Created Date:  2011-01-21     Completed Date:  2011-02-25     Revised Date:  2012-02-03    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  United States    
Other Details:
Languages:  eng     Pagination:  374-83     Citation Subset:  AIM; IM    
Affiliation:
Samuel Lunenfeld Research Institute Mt Sinai Hospital, 600 University Avenue TCP5-1004, Toronto, Ontario, Canada.
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MeSH Terms
Descriptor/Qualifier:
Animals
Blood Glucose / genetics,  metabolism*
Gastric Emptying / drug effects,  genetics
Gastric Inhibitory Polypeptide / blood
Glucagon / blood
Glucagon-Like Peptide 1 / blood
Glucose Tolerance Test
Insulin / blood
Islets of Langerhans / drug effects,  metabolism
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Oxadiazoles / pharmacology
Pyrimidines / pharmacology
Receptors, G-Protein-Coupled / genetics,  metabolism*
Receptors, Gastrointestinal Hormone / genetics,  metabolism*
Grant Support
ID/Acronym/Agency:
14799//Canadian Institutes of Health Research; 82700//Canadian Institutes of Health Research; 82700//Canadian Institutes of Health Research; MOP-14799//Canadian Institutes of Health Research
Chemical
Reg. No./Substance:
0/AR 231453; 0/Blood Glucose; 0/Gpr119 protein, mouse; 0/Insulin; 0/Oxadiazoles; 0/Pyrimidines; 0/Receptors, G-Protein-Coupled; 0/Receptors, Gastrointestinal Hormone; 59392-49-3/Gastric Inhibitory Polypeptide; 89750-14-1/Glucagon-Like Peptide 1; 9007-92-5/Glucagon

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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