葛兰素史克-3
糖原合酶
神经病理学
神经毒性
阿尔茨海默病
神经科学
激酶
τ蛋白
生物
GSK3B公司
神经退行性变
蛋白激酶A
疾病
医学
糖原
生物化学
内科学
毒性
作者
Miguel Medina,Jesús Ávila
标识
DOI:10.2174/138161210793176581
摘要
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.
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