Glycogen Synthase Kinase-3 (GSK-3) Inhibitors for the Treatment of Alzheimer's Disease

被引:77
|
作者
Medina, Miguel [2 ]
Avila, Jesus [1 ]
机构
[1] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, CSIC, E-28049 Madrid, Spain
[2] Noscira SA, Tres Cantos 28760, Madrid, Spain
基金
美国国家科学基金会;
关键词
GSK-3; Alzheimer's disease; Tau; amyloid; neurodegeneration; lithium; memory; neuroinflammation; AMYLOID PRECURSOR PROTEIN; RABBIT SKELETAL-MUSCLE; RESPONSE MEDIATOR PROTEINS; TRANSGENIC MICE; TAU-HYPERPHOSPHORYLATION; BETA-CATENIN; NEUROFIBRILLARY TANGLES; LYSOPHOSPHATIDIC ACID; POTENT INHIBITORS; SIGNALING PATHWAY;
D O I
10.2174/138161210793176581
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Originally discovered because of its role in the regulation of glucose metabolism, Glycogen Synthase Kinase-3 (GSK-3) 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 A beta neurotoxicity, plays an essential role in synaptic plasticity and memory, might be involved in A beta 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 for the therapeutic intervention in neurodegenerative diseases as well as a means to understand the molecular basis of these disorders.
引用
收藏
页码:2790 / 2798
页数:9
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