Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2839311 | Trends in Molecular Medicine | 2008 | 8 Pages |
Abstract
Incretins, enhancers of insulin secretion, are essential for glucose tolerance, and a reduction in their function might contribute to poor β-cell function in patients with type-2 diabetes mellitus. However, at supraphysiological doses, the incretin glucagon-like peptide-1 (GLP-1) protects pancreatic β 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.
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Authors
Jens J. Holst, Carolyn F. Deacon, Tina Vilsbøll, Thure Krarup, Sten Madsbad,