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用于糖尿病治疗的葡萄糖激酶激活剂的研发:理论与实践层面

Research and development of glucokinase activators for diabetes therapy: theoretical and practical aspects.

作者信息

Matschinsky Franz M, Zelent Bogumil, Doliba Nicolai M, Kaestner Klaus H, Vanderkooi Jane M, Grimsby Joseph, Berthel Steven J, Sarabu Ramakanth

机构信息

Department of Biochemistry and Biophysics, University of Pennsylvania, Institute for Diabetes, Obesity and Metabolism, 415 Curie Blvd, 605 CRB, Philadelphia, PA 19104, USA.

出版信息

Handb Exp Pharmacol. 2011(203):357-401. doi: 10.1007/978-3-642-17214-4_15.

Abstract

Glucokinase Glucokinase (GK GK ; EC 2.7.1.1.) phosphorylates and regulates glucose metabolism in insulin-producing pancreatic beta-cells, hepatocytes, and certain cells of the endocrine and nervous systems allowing it to play a central role in glucose homeostasis glucose homeostasis . Most importantly, it serves as glucose sensor glucose sensor in pancreatic beta-cells mediating glucose-stimulated insulin biosynthesis and release and it governs the capacity of the liver to convert glucose to glycogen. Activating and inactivating mutations of the glucokinase gene cause autosomal dominant hyperinsulinemic hypoglycemia and hypoinsulinemic hyperglycemia in humans, respectively, illustrating the preeminent role of glucokinase in the regulation of blood glucose and also identifying the enzyme as a potential target for developing antidiabetic drugs antidiabetic drugs . Small molecules called glucokinase activators (GKAs) glucokinase activators (GKAs) which bind to an allosteric activator allosteric activator site of the enzyme have indeed been discovered and hold great promise as new antidiabetic agents. GKAs increase the enzyme's affinity for glucose and also its maximal catalytic rate. Consequently, they stimulate insulin biosynthesis and secretion, enhance hepatic glucose uptake, and augment glucose metabolism and related processes in other glucokinase-expressing cells. Manifestations of these effects, most prominently a lowering of blood glucose, are observed in normal laboratory animals and man but also in animal models of diabetes and patients with type 2 diabetes mellitus (T2DM T2DM ) type 2 diabetes mellitus (T2DM) . These compelling concepts and results sustain a strong R&D effort by many pharmaceutical companies to generate GKAs with characteristics allowing for a novel drug treatment of T2DM.

摘要

葡萄糖激酶 葡萄糖激酶(GK;EC 2.7.1.1.)可磷酸化并调节胰岛素分泌性胰腺β细胞、肝细胞以及内分泌和神经系统某些细胞中的葡萄糖代谢,使其在葡萄糖稳态中发挥核心作用。最重要的是,它在胰腺β细胞中作为葡萄糖传感器,介导葡萄糖刺激的胰岛素生物合成和释放,并且控制肝脏将葡萄糖转化为糖原的能力。葡萄糖激酶基因的激活和失活突变分别导致人类常染色体显性高胰岛素血症性低血糖症和低胰岛素血症性高血糖症,这说明了葡萄糖激酶在血糖调节中的卓越作用,也将该酶确定为开发抗糖尿病药物的潜在靶点。确实已发现一种称为葡萄糖激酶激活剂(GKAs)的小分子,它与该酶的变构激活剂位点结合,并作为新型抗糖尿病药物具有很大潜力。GKAs增加了该酶对葡萄糖的亲和力及其最大催化速率。因此,它们刺激胰岛素生物合成和分泌,增强肝脏对葡萄糖的摄取,并增强其他表达葡萄糖激酶的细胞中的葡萄糖代谢及相关过程。在正常实验动物和人类中,以及在糖尿病动物模型和2型糖尿病(T2DM)患者中都观察到了这些作用的表现,最显著的是血糖降低。这些引人注目的概念和结果促使许多制药公司大力开展研发工作,以开发具有可用于新型药物治疗T2DM特性的GKAs。

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