Assessing the potential of glucokinase activators in diabetes therapy

被引:338
作者
Matschinsky, Franz M. [1 ]
机构
[1] Univ Penn, Sch Med, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GLUCAGON-LIKE PEPTIDE-1; PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA; INDUCED INSULIN-RESISTANCE; PANCREATIC-ISLET TISSUE; BETA-CELL HYPERPLASIA; ACID-INDUCED GLUCAGON; REGULATORY PROTEIN; LIVER GLUCOKINASE; GLUCOSE-HOMEOSTASIS; FASTING GLUCOSE;
D O I
10.1038/nrd2850
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glucokinase, a unique isoform of the hexokinase enzymes, which are known to phosphorylate D-glucose and other hexoses, was identified during the past three to four decades as a new, promising drug target for type 2 diabetes. Glucokinase serves as a glucose sensor of the insulin-producing pancreatic islet beta-cells, controls the conversion of glucose to glycogen in the liver and regulates hepatic glucose production. Guided by this fundamental knowledge, several glucokinase activators are now being developed, and have so far been shown to lower blood glucose in several animal models of type 2 diabetes and in initial trials in humans with the disease. Here, the scientific basis and current status of this new approach to diabetes therapy are discussed.
引用
收藏
页码:399 / 416
页数:18
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