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.
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