Glucagon-like peptide-1, glucose homeostasis and diabetes

被引:128
|
作者
Holst, Jens J. [1 ,4 ,5 ]
Deacon, Carolyn F. [1 ]
Vilsboll, Tina [2 ]
Krarup, Thure [2 ]
Madsbad, Sten [3 ]
机构
[1] Univ Copenhagen, Panum Inst, Dept Biomed Sci, DK-2200 Copenhagen, Denmark
[2] Univ Hosp, Dept Internal Med F, DK-2900 Copenhagen, Denmark
[3] Hvidovre Univ Hosp, Dept Endocrinol, DK-2650 Hvidovre, Denmark
[4] Novo Nordisk AS, Copenhagen, Denmark
[5] Merck Sharp & Dohme Ltd, Copenhagen, Denmark
关键词
D O I
10.1016/j.molmed.2008.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Incretins, enhancers of insulin secretion, are essential for glucose tolerance, and a reduction in their function might contribute to poor P-cell function in patients with type-2 diabetes mellitus. However, at supraphysiollogical doses, the incretin glucagon-like peptide-1 (GLP-1) protects pancreatic P 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 pathophysiollogical basis the clinical use of these therapeutics is reviewed here.
引用
收藏
页码:161 / 168
页数:8
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