Revisiting AMPA Receptors as an Antiepileptic Drug Target

被引:241
作者
Rogawski, Michael A. [1 ,2 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Neurol, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Ctr Neurosci, Sacramento, CA 95817 USA
关键词
METHYL-D-ASPARTATE; GLUR5 KAINATE RECEPTORS; NON-NMDA RECEPTORS; EPILEPTIFORM ACTIVITY; GLUTAMATE RECEPTORS; KINDLING MODEL; AMINO-ACIDS; ANTAGONISTS; ANTICONVULSANT; GYKI-52466;
D O I
10.5698/1535-7511-11.2.56
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In the 1990s there was intense interest in ionotropic glutamate receptors as therapeutic targets for diverse neurological disorders, including epilepsy. NMDA receptors were thought to play a key role in the generation of seizures, leading to clinical studies of NMDA receptor blocking drugs in epilepsy. Disappointing results dampened enthusiasm for ionotropic glutamate receptors as a therapeutic target. Eventually it became appreciated that another type of ionotropic glutamate receptor, the AMPA receptor, is actually the predominant mediator of excitatory neurotransmission in the central nervous system and moreover that AMPA receptors are critical to the generation and spread of epileptic activity. As drugs became available that selectively target AMPA receptors, it was possible to demonstrate that AMPA receptor antagonists have powerful antiseizure activity in in vitro and in vivo models. A decade later, promising clinical studies with AMPA receptor antagonists, including the potent noncompetitive antagonist perampanel, are once again focusing attention on AMPA receptors as a drug target for epilepsy therapy.
引用
收藏
页码:56 / 63
页数:8
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