Involvement of cAMP/EPAC/TRPM2 activation in glucose- and incretin-induced insulin secretion

Diabetes. 2014 Oct;63(10):3394-403. doi: 10.2337/db13-1868. Epub 2014 May 13.

Abstract

In pancreatic β-cells, closure of the ATP-sensitive K(+) (K(ATP)) channel is an initial process triggering glucose-stimulated insulin secretion. In addition, constitutive opening of background nonselective cation channels (NSCCs) is essentially required to effectively evoke depolarization as a consequence of K(ATP) channel closure. Thus, it is hypothesized that further opening of NSCC facilitates membrane excitability. We identified a class of NSCC that was activated by exendin (ex)-4, GLP-1, and its analog liraglutide at picomolar levels. This NSCC was also activated by increasing the glucose concentration. NSCC activation by glucose and GLP-1 was a consequence of the activated cAMP/EPAC-mediated pathway and was attenuated in TRPM2-deficient mice. The NSCC was not activated by protein kinase A (PKA) activators and was activated by ex-4 in the presence of PKA inhibitors. These results suggest that glucose- and incretin-activated NSCC (TRPM2) works in concert with closure of the KATP channel to effectively induce membrane depolarization to initiate insulin secretion. The current study reveals a new mechanism for regulating electrical excitability in β-cells and for mediating the action of glucose and incretin to evoke insulin secretion, thereby providing an innovative target for the treatment of type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / analogs & derivatives*
  • Acetylcysteine / metabolism
  • Animals
  • Calcium / metabolism
  • Cyclic AMP / metabolism*
  • Erythromycin / analogs & derivatives*
  • Erythromycin / metabolism
  • Exenatide
  • Glucose / pharmacology
  • Incretins / pharmacology
  • Insulin / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Male
  • Mice
  • Mice, Knockout
  • Peptides / pharmacology
  • Rats, Wistar
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • TRPM Cation Channels / metabolism*
  • Venoms / pharmacology

Substances

  • Incretins
  • Insulin
  • Peptides
  • TRPM Cation Channels
  • TRPM2 protein, mouse
  • Venoms
  • Erythromycin
  • erythromycin propionate-N-acetylcysteinate
  • Exenatide
  • Cyclic AMP
  • Glucose
  • Calcium
  • Acetylcysteine