Effects of valproate, phenytoin, and zonisamide on clonic and tonic seizures induced by acute and repeated exposure of mice to flurothyl

被引:12
作者
Hashimoto, Y
Araki, H [1 ]
Futagami, K
Kawasaki, H
Gomita, Y
机构
[1] Ehime Univ, Sch Med, Dept Hosp Pharm, Onsen, Ehime 7910295, Japan
[2] Okayama Univ, Sch Med, Dept Hosp Pharm, Okayama 7008558, Japan
[3] Okayama Univ, Dept Clin Pharmaceut Sci, Fac Pharmaceut Sci, Okayama 7008558, Japan
关键词
flurothyl kindling model; seizure phenotype; valproate; zonisamide; phenytoin; mice;
D O I
10.1016/S0031-9384(03)00013-1
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
The effects of valproate (WA), zonisamide (ZNS), and phenytoin (PHT) on flurothyl (FE)-induced generalized seizure were investigated in mice. In the FE kindling model, eight daily FE-induced generalized clonic seizures followed by a 28-day stimulation-free interval converted the type of seizure expressed in response to FE from clonic to tonic. In an acute FE trial experiment, the latencies of clonic and tonic seizures were prolonged significantly and dose-dependently by the administration of VIA. ZNS and PHT did not show any effect on the latencies of tonic seizure. When the same three drugs were administered to mice daily for 8 days prior to the FE trial, changes in the seizure phenotypes from clonic to tonic seizure were significantly inhibited by VIA and ZNS, but not by PHT. These results suggest that VIA and ZNS possess significant antiepileptogenic properties. PHT apparently does not share this property to the same degree in the present FE-induced model. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:465 / 469
页数:5
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