Johnson D, Shepherd R M, Gill D, Gorman T, Smith D M, Dunne M J
Faculty of Life Sciences, University of Manchester, Core Technology Facility, 46 Grafton Street, Manchester M13 9NT, U.K.
Biochem Soc Trans. 2007 Nov;35(Pt 5):1208-10. doi: 10.1042/BST0351208.
GK (glucokinase) catalyses the phosphorylation of glucose to glucose 6-phosphate in glucosensitive cells. In pancreatic beta-cells, this reaction is the rate-limiting step of insulin release. Recent work has led to the discovery of synthetic small-molecule activators of GK that stimulate beta-cell physiology and subsequently enhance the glucose-dependent release of insulin. It is currently recognized that these compounds may represent a significant advance in the development of new agents in the treatment of diabetes. In addition, GKAs (GK activators) are emerging as reagents that are useful tools with which to probe the function of pancreatic beta-cells and other glucosensitive cells. This includes providing insights into the physiology of the beta-cell by helping to elucidate the kinetic cycle of GK, confirming the central role of glucose metabolism to the beta-cell and highlighting subtle species-dependent differences in insulin secretion between rodent and human islets of Langerhans.
葡萄糖激酶(GK)在葡萄糖敏感细胞中催化葡萄糖磷酸化为6-磷酸葡萄糖。在胰腺β细胞中,该反应是胰岛素释放的限速步骤。最近的研究发现了GK的合成小分子激活剂,这些激活剂可刺激β细胞生理功能,进而增强胰岛素的葡萄糖依赖性释放。目前认为,这些化合物可能代表了糖尿病治疗新药开发的重大进展。此外,GK激活剂(GKAs)正成为一种试剂,是用于探究胰腺β细胞和其他葡萄糖敏感细胞功能的有用工具。这包括通过帮助阐明GK的动力学循环来深入了解β细胞的生理学,确认葡萄糖代谢对β细胞的核心作用,并突出啮齿动物和人类胰岛在胰岛素分泌方面细微的物种依赖性差异。