Effects of anti-epileptic drugs on glutamine synthetase activity in mouse brain

被引:39
作者
Fraser, CM [1 ]
Sills, GJ [1 ]
Forrest, G [1 ]
Thompson, GG [1 ]
Brodie, MJ [1 ]
机构
[1] Univ Glasgow, Western Infirm, Epilepsy Unit, Dept Med & Therapeut, Glasgow G11 6NT, Lanark, Scotland
关键词
anti-epileptic drugs; epilepsy; glutamine synthetase;
D O I
10.1038/sj.bjp.0702472
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Glutamine synthetase (GS) is a key enzyme in the regulation of glutamate neurotransmission in the central nervous system. It is responsible for the conversion of glutamate to glutamine, and for the detoxification of ammonia. 2 We have investigated the effects of single and repeated intraperitoneal administration of a range of established and new anti-epileptic drugs on GS activity in mouse brain. 3 Four hours after the final dose, animals were sacrificed and the brains removed for analysis of GS activity. 4 Both single and repeated doses of phenytoin and carbamazepine were found to reduce enzyme activity (P<0.05). 5 Single doses of phenobarbitone, felbamate and topiramate were without effect, however repeated administration of these drugs dose-dependently reduced GS activity (P<0.05). 6 Single and repeated doses of sodium valproate, vigabatrin, lamotrigine, gabapentin, tiagabine, levetiracetam and desglycinyl-remacemide were found to have no effect on GS activity. 7 The reduction in enzyme activity demonstrated is unlikely to be related to the anti-epileptic actions of these drugs, but may contribute to their toxicity.
引用
收藏
页码:1634 / 1638
页数:5
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