[GLP-1-based treatment of type 2 diabetes mellitus]

Ugeskr Laeger. 2007 May 28;169(22):2095-9.
[Article in Danish]

Abstract

GLP-1 is secreted from the small intestine in response to ingestion of nutrients. It has a powerful insulinotropic effect and stimulates beta-cell growth and is therefore being developed for treatment of type 2 diabetes. The GLP-1 analogue, exenatide, is on the market in the USA as an add-on therapy. Another strategy to increase circulating GLP-1 is to inhibit the enzyme DPP-IV which degrades endogenous GLP-1. GLP-1-based therapy results in HbA1c reductions of approximately 1 percent point, and the lack of serious side effects and the low risk of hypoglycaemic episodes are unique traits.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Count
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / antagonists & inhibitors
  • Eating / physiology
  • Exenatide
  • Glucagon-Like Peptide 1 / administration & dosage
  • Glucagon-Like Peptide 1 / metabolism
  • Glucagon-Like Peptide 1 / therapeutic use*
  • Humans
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / therapeutic use*
  • Insulin-Secreting Cells / drug effects
  • Intestine, Small / metabolism
  • Peptides / administration & dosage
  • Peptides / therapeutic use*
  • Venoms / administration & dosage
  • Venoms / therapeutic use*

Substances

  • Hypoglycemic Agents
  • Peptides
  • Venoms
  • Glucagon-Like Peptide 1
  • Exenatide
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases