Influence of glucagon-like peptide-1 on beta cell responsiveness

Regul Pept. 1993 Apr 8;44(3):277-83. doi: 10.1016/0167-0115(93)90137-w.

Abstract

The postulated incretin factor glucagon-like peptide-1 (GLP-1) causes a glucose-dependent increase in insulin secretion from perifused rat islets. In the presence of 6 mM glucose the response to 10 nM GLP-1 is characterized by a large initial spike of secretion, followed by a brief, slowly rising phase. However, after 30-40 min of stimulation, this phase subsides to prestimulatory secretory rates. Raising the glucose level to 8 mM, however, amplifies and sustains the stimulatory effect of 10 nM GLP-1. The response to GLP-1 (10 nM) in the presence of 8 mM glucose is abolished by the metabolic inhibitor mannoheptulose (15 mM), and reduced by the calcium channel antagonist nitrendipine (5 microM), or the protein kinase C inhibitor of staurosporine (20 nM). A significant synergistic effect of GLP-1 (10 nM) and 10 microM carbachol, a cholinergic agonist, on insulin secretion was observed in the presence of 6 mM glucose. In the presence of either 6 or 8 mM glucose, GLP-1 (10 nM) has no significant effect on glucose usage or on inositol phosphate generation in [3H]inositol prelabeled islets. The results support the concept that GLP-1 may function as an important physiologic incretin factor, particularly when accompanied by agonists that activate phosphoinositide hydrolysis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carbachol / pharmacology
  • Cholecystokinin / pharmacology
  • Dose-Response Relationship, Drug
  • Gastric Inhibitory Polypeptide / pharmacology
  • Glucagon / pharmacology*
  • Glucagon / physiology
  • Glucagon-Like Peptide 1
  • Glucose / antagonists & inhibitors
  • Glucose / metabolism
  • Glucose / pharmacology
  • Insulin / metabolism
  • Insulin Secretion
  • Islets of Langerhans / drug effects*
  • Islets of Langerhans / metabolism*
  • Male
  • Mannoheptulose / pharmacology
  • Peptide Fragments / pharmacology*
  • Peptide Fragments / physiology
  • Phosphorylation / drug effects
  • Protein Precursors / pharmacology*
  • Protein Precursors / physiology
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Insulin
  • Peptide Fragments
  • Protein Precursors
  • Gastric Inhibitory Polypeptide
  • Mannoheptulose
  • Glucagon-Like Peptide 1
  • Carbachol
  • Glucagon
  • Cholecystokinin
  • Glucose