GSK-3 inhibitors: preclinical and clinical focus on CNS

被引:279
|
作者
Eldar-Finkelman, Hagit [1 ]
Martinez, Ana [2 ]
机构
[1] Tel Aviv Univ, Sackler Sch Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, Israel
[2] CSIC, Inst Quim Med, E-28006 Madrid, Spain
来源
FRONTIERS IN MOLECULAR NEUROSCIENCE | 2011年 / 4卷
关键词
protein kinases; GSK-3; inhibitors; CNS; GLYCOGEN-SYNTHASE KINASE-3; NEURONAL CELL-DEATH; BETA-CATENIN STABILIZATION; SMALL-MOLECULE INHIBITORS; CYCLIN-DEPENDENT KINASES; INSULIN-MIMETIC ACTION; WNT SIGNALING PATHWAY; EMBRYONIC STEM-CELLS; PROTEIN-KINASE; ALZHEIMERS-DISEASE;
D O I
10.3389/fnmol.2011.00032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Inhibiting glycogen synthase kinase-3 (GSK-3) activity via pharmacological intervention has become an important strategy for treating neurodegenerative and psychiatric disorders. The known GSK-3 inhibitors are of diverse chemotypes and mechanisms of action and include compounds isolated from natural sources, cations, synthetic small-molecule ATP-competitive inhibitors, non-ATP-competitive inhibitors, and substrate competitive inhibitors. Here we describe the variety of GSK-3 inhibitors with a specific emphasis on their biological activities in neurons and neurological disorders. We further highlight our current progress in the development of non-ATP-competitive inhibitors of GSK-3. The available data raise the hope that one or more of these drug design approaches will prove successful at stabilizing or even reversing the aberrant neuropathology and cognitive deficits of certain central nervous system disorders.
引用
收藏
页数:18
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