Dailey J W, Reith M E, Yan Q S, Li M Y, Jobe P C
Department of Biomedical and Therapeutic Sciences, University of Illinois College of Medicine at Peoria, 61656, USA.
Neurosci Lett. 1997 May 9;227(1):13-6. doi: 10.1016/s0304-3940(97)00288-7.
The antiepileptic drug carbamazepine produces dose related anticonvulsant effects in genetically epilepsy-prone rats (GEPRs) and most other animal seizure models. Carbamazepine releases serotonin as part of the pharmacodynamic action by which it suppresses convulsions in GEPRs and it releases serotonin in non-epileptic Sprague-Dawley rats. The two strains which make up the GEPR seizure model (moderate seizure GEPR-3s and severe seizure GEPR-9s) experience anticonvulsant effects in response to different doses of carbamazepine (GEPR-3 ED50 = 25 mg/kg; GEPR-9 ED50 = 3 mg/kg). The present study determined that carbamazepine produces a dose related increase in extracellular serotonin in each of the two GEPR strains. The doses of carbamazepine required to increase extracellular serotonin are similar to the doses required for an anticonvulsant effect in each of the strains. This result provides further support for the hypothesis that release of serotonin by carbamazepine is an important part of the pharmacodynamic action by which this drug suppresses seizures.
抗癫痫药物卡马西平在遗传性癫痫易感大鼠(GEPRs)和大多数其他动物癫痫模型中产生剂量相关的抗惊厥作用。卡马西平释放5-羟色胺作为其药效学作用的一部分,通过这种作用它抑制GEPRs中的惊厥,并且它在非癫痫性的斯普拉格-道利大鼠中也释放5-羟色胺。构成GEPR癫痫模型的两个品系(中度癫痫发作的GEPR-3s和重度癫痫发作的GEPR-9s)对不同剂量的卡马西平产生抗惊厥作用(GEPR-3的半数有效剂量=25毫克/千克;GEPR-9的半数有效剂量=3毫克/千克)。本研究确定卡马西平在两个GEPR品系的每一个中都产生剂量相关的细胞外5-羟色胺增加。增加细胞外5-羟色胺所需的卡马西平剂量与每个品系产生抗惊厥作用所需的剂量相似。这一结果为卡马西平释放5-羟色胺是该药物抑制癫痫发作的药效学作用的重要组成部分这一假说提供了进一步的支持。