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Glucagon-like peptide-1, glucose homeostasis and diabetes

Jens Juul Holst, Carolyn F. Deacon, Tina Vilsbøll, Thure Krarup, Sten Madsbad

160 Citations (Scopus)

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.
Original languageEnglish
JournalTrends in Molecular Medicine
Volume14
Issue number4
Pages (from-to)161-8
Number of pages8
ISSN1471-4914
DOIs
Publication statusPublished - 1 Apr 2008

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