| Literature DB >> 18353723 |
Jens J Holst1, Carolyn F Deacon, Tina Vilsbøll, Thure Krarup, Sten Madsbad.
Abstract
Incretins, enhancers of insulin secretion, are essential for glucose tolerance, and a reduction in their function might contribute to poor beta-cell function in patients with type-2 diabetes mellitus. However, at supraphysiological doses, the incretin glucagon-like peptide-1 (GLP-1) protects pancreatic beta cells, and inhibits glucagon secretion, gastric emptying and food intake, leading to weight loss. GLP-1 mimetics, which are stable-peptide-based activators of the GLP-1 receptor, and incretin enhancers, which inhibit the incretin-degrading enzyme dipeptidyl peptidase-4, have emerged as therapies for type-2 diabetes and have recently reached the market. The pathophysiological basis the clinical use of these therapeutics is reviewed here.Entities:
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Year: 2008 PMID: 18353723 DOI: 10.1016/j.molmed.2008.01.003
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951