Mazarati Andrey M, Sofia R Duane, Wasterlain Claude G
Department of Neurology, UCLA School of Medicine, Los Angeles, CA, USA.
Seizure. 2002 Oct;11(7):423-30. doi: 10.1053/seiz.2002.0677.
To examine the seizure-protective properties of fluorofelbamate, a felbamate analog, on acute and chronic seizures in an experimental model of self-sustaining status epilepticus (SSSE).
SSSE was induced by stimulation of the perforant path for 30 min (PPS) through chronically implanted electrodes in free-running adult male Wistar rats. Fluorofelbamate was injected intravenously (i.v.) either 10 min, or 40 min after SSSE induction. Seizure and spike profiles were analyzed off-line.
Fluorofelbamate injected during the early stages of SSSE (10 min after the end of PPS), shortened the duration of seizures in a dose-dependent manner. While a dose of 50 mg kg(-1) was ineffective, 100 and 200 mg kg(-1) reduced cumulative seizure time from 393 +/- 10 min to 15 +/- 8 min and 2.4 +/- 0.5 min respectively. Administration of fluorofelbamate (200 and 300 mg kg (-1)) at a late stage of SSSE, which is refractory to treatment with conventional anticonvulsants, also significantly attenuated seizures. Acute fluorofelbamate treatment (200 mg kg(-1) 10 min after PPS) significantly decreased the frequency of spontaneous seizures which follow SSSE after a 'latent' interval. Moreover, in contrast to control animals, fluorofelbamate-treated rats showed regression of spontaneous seizures, and an apparent remission of epilepsy within 2 months after SSSE.
Acute treatment of SSSE with fluorofelbamate showed strong anticonvulsant effects even during the late stages of SSSE. In this model, it also displayed antiepileptogenic properties: it reduced the severity of chronic epilepsy after SSSE and lead to apparent remissions of that epilepsy.
在自我维持性癫痫持续状态(SSSE)实验模型中,研究氟非氨酯(一种非氨酯类似物)对急性和慢性癫痫发作的保护特性。
通过慢性植入电极刺激成年雄性自由活动的Wistar大鼠的穿通通路30分钟(PPS)来诱导SSSE。在SSSE诱导后10分钟或40分钟静脉注射氟非氨酯。离线分析癫痫发作和棘波情况。
在SSSE早期(PPS结束后10分钟)注射氟非氨酯,可剂量依赖性地缩短癫痫发作持续时间。50mg/kg剂量无效,而100mg/kg和200mg/kg分别将累积癫痫发作时间从393±10分钟减少到15±8分钟和2.4±0.5分钟。在SSSE后期给予氟非氨酯(200mg/kg和300mg/kg),此时对传统抗惊厥药物治疗无效,也能显著减轻癫痫发作。急性氟非氨酯治疗(PPS后10分钟给予200mg/kg)可显著降低SSSE后“潜伏”期出现的自发性癫痫发作频率。此外,与对照动物相比,氟非氨酯治疗的大鼠自发性癫痫发作出现消退,并且在SSSE后2个月内癫痫明显缓解。
用氟非氨酯急性治疗SSSE即使在SSSE后期也显示出强大的抗惊厥作用。在该模型中,它还表现出抗癫痫发生特性:降低了SSSE后慢性癫痫的严重程度并导致该癫痫明显缓解。