Glutamate in CNS disorders as a target for drug development: An update

被引:366
作者
Parsons, CG
Danysz, W
Quack, G
机构
[1] Merz & Co, Behav & Electrophysiol Sect, Frankfurt, Germany
[2] Merz & Co, Preclin Res, Frankfurt, Germany
关键词
D O I
10.1358/dnp.1998.11.9.863689
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The authors provide an extensive review of new data related to the role of glutamate in CNS disorders, describing new aspects in glutamate and glutamatergic receptors-NMDA receptors, NR2B-selective antagonists, non-NMDA ionotropic glutamate receptors, N-acetylaspartylglutamate, and glutamate and glycine transporters. New findings in animal models and in human diseases-stroke, traumatic brain injury, Alzheimer's, Parkinson's and Huntington's diseases, tardive dyskinesia, ALS, olivopontcerebellar degeneration, AIDS, allergic encephalomyelitis, epilepsy. anxiety, depression, schizophrenia, liver disease, aminoglycoside antibiotic-induced hearing loss, hemiplegia, chronic pain and drug tolerance and abuse-are presented. Finally, the authors cite the progress achieved in the development of agents that interact with the glutamatergic system: NMDA channel blockers, competitive NMDA receptor antagonists, NR2B-selective antagonists, glutamate release inhibitors, glycine(B) antagonists, AMPA and kainate receptor antagonists, AMPA receptor-positive modulators and agents that act by modifying endogenous kynurenic acid metabolism. (C) 1998 Prous Science. All rights reserved.
引用
收藏
页码:523 / 569
页数:47
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