葡萄糖激酶
内分泌学
内科学
葡萄糖稳态
变构调节
糖尿病
碳水化合物代谢
胰岛
胰岛素
小岛
化学
血糖调节
平衡
酶
生物
2型糖尿病
医学
生物化学
胰岛素抵抗
作者
Joseph Grimsby,Ramakanth Sarabu,Wendy L. Corbett,Nancy-Ellen Haynes,Fred T. Bizzarro,John W. Coffey,Kevin R. Guertin,Darryl W. Hilliard,Robert F. Kester,Paige E. Mahaney,Linda Marcus,Lida Qi,Cheryl Spence,J. P. TENGI,Mark A. Magnuson,Chang An Chu,Mark Dvorozniak,Franz M. Matschinsky,Joseph F. Grippo
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2003-07-17
卷期号:301 (5631): 370-373
被引量:527
标识
DOI:10.1126/science.1084073
摘要
Glucokinase (GK) plays a key role in whole-body glucose homeostasis by catalyzing the phosphorylation of glucose in cells that express this enzyme, such as pancreatic β cells and hepatocytes. We describe a class of antidiabetic agents that act as nonessential, mixed-type GK activators (GKAs) that increase the glucose affinity and maximum velocity ( V max ) of GK. GKAs augment both hepatic glucose metabolism and glucose-induced insulin secretion from isolated rodent pancreatic islets, consistent with the expression and function of GK in both cell types. In several rodent models of type 2 diabetes mellitus, GKAs lowered blood glucose levels, improved the results of glucose tolerance tests, and increased hepatic glucose uptake. These findings may lead to the development of new drug therapies for diabetes.
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