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Curr Pharm Des. 2010;16(25):2790-8. doi: 10.2174/138161210793176581.
Originally discovered because of its role in the regulation of glucose metabolism, Glycogen Synthase Kinase-3 (GSK-3) it is now recognised as a crucial player in a diverse series of cellular processes involved in Alzheimer's disease (AD) pathology. Besides having been identified as the major tau protein kinase, GSK-3 mediates Aβ neurotoxicity, plays an essential role in synaptic plasticity and memory, might be involved in Aβ formation, and it has an important role in inflammation and neuronal survival, all key features of AD neuropathology. Moreover, AD was one of the earliest disorders linked to GSK-3 dysfunction. Thus, the discovery of small molecule GSK-3 inhibitors has attracted significant attention to the protein both as therapeutic target for the therapeutic intervention in neurodegenerative diseases as well as a means to understand the molecular basis of these disorders.
最初因其在葡萄糖代谢调节中的作用而被发现,糖原合成酶激酶-3(GSK-3)现在被认为是阿尔茨海默病(AD)病理中涉及多种细胞过程的关键参与者。除了被确定为主要的 tau 蛋白激酶外,GSK-3 还介导 Aβ 神经毒性,在突触可塑性和记忆中发挥重要作用,可能参与 Aβ 的形成,并且在炎症和神经元存活中具有重要作用,这些都是 AD 神经病理学的关键特征。此外,AD 是最早与 GSK-3 功能障碍相关的疾病之一。因此,小分子 GSK-3 抑制剂的发现引起了人们对该蛋白的极大关注,它既是神经退行性疾病治疗干预的治疗靶点,也是理解这些疾病分子基础的一种手段。