[Glucagon-like peptide-1: a cardiological perspective]

Ugeskr Laeger. 2010 Oct 11;172(41):2822-6.
[Article in Danish]

Abstract

Increasing experimental evidence points to direct effects of glucagon-like peptide-1 (GLP-1) and its analogs on the heart and circulatory system, in addition to the well-established, antidiabetic actions of these agents on glucose and on the energy metabolism. These effects are primarily vasodilation, diminished heart muscle loss after myocardial infarction and a contractility increase of a weak left ventricle. A few, small patient trials appear to support the latter effect. Experimental results suggest the myocardium-saving effect following coronary occlusion and reperfusion as particularly suitable for clinical testing.

Publication types

  • Review

MeSH terms

  • Cardiomyopathy, Dilated / drug therapy
  • Cardiovascular System / drug effects*
  • Cardiovascular System / metabolism
  • Energy Metabolism / drug effects
  • Exenatide
  • Glucagon-Like Peptide 1 / analogs & derivatives
  • Glucagon-Like Peptide 1 / pharmacology
  • Glucagon-Like Peptide 1 / physiology*
  • Glucagon-Like Peptide 1 / therapeutic use
  • Glucagon-Like Peptide-1 Receptor
  • Heart / drug effects
  • Humans
  • Hypoglycemic Agents / pharmacology*
  • Hypoglycemic Agents / therapeutic use
  • Liraglutide
  • Myocardial Reperfusion Injury / drug therapy
  • Myocardium / metabolism
  • Peptides / pharmacology
  • Peptides / therapeutic use
  • Receptors, Glucagon / drug effects
  • Receptors, Glucagon / metabolism
  • Venoms / pharmacology
  • Venoms / therapeutic use

Substances

  • GLP1R protein, human
  • Glucagon-Like Peptide-1 Receptor
  • Hypoglycemic Agents
  • Peptides
  • Receptors, Glucagon
  • Venoms
  • Liraglutide
  • Glucagon-Like Peptide 1
  • Exenatide