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托吡酯对快速点燃形成及维持的年龄依赖性影响。

Age-dependent effects of topiramate on the acquisition and the retention of rapid kindling.

作者信息

Mazarati Andréy, Shin Don, Auvin Stéphane, Sankar Raman

机构信息

Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-1752, USA.

出版信息

Epilepsia. 2007 Apr;48(4):765-73. doi: 10.1111/j.1528-1167.2007.00987.x. Epub 2007 Feb 23.

Abstract

PURPOSE

To examine antiepileptogenic, disease modifying, and anticonvulsant effects of topiramate under conditions of rapid kindling at different stages of development.

METHODS

Afterdischarge threshold (ADT) and duration (ADD) were examined in 2-, 3-, and 5-week-old Wistar rats before and after administration of topiramate (200 mg/kg). Animals underwent a rapid kindling protocol (sixty 10-s trains, bipolar 20 Hz square wave pulses delivered every 5 min). The progression of behavioral and electrographic seizures, and responses to test stimulations 24 h after the protocol were compared between topiramate and vehicle-treated control rats. In addition, rats that were previously given vehicle only prior to kindling, were then given topiramate to examine the effect on established kindled seizures.

RESULTS

In 2-week-old animals, topiramate affected neither the baseline afterdischarge, nor the progression of kindled seizures. In 3-week-old rats, topiramate did not modify the baseline afterdischarge, but significantly delayed the occurrence of full motor seizures in response to repeated stimulations. Topiramate treatment of 5-week-old rats increased baseline ADT, shortened ADD, and delayed the progression of kindled seizures. Twenty-four h after the last kindling stimulation, animals of all ages exhibited a decreased ADT, an increase ADD, and developed behavioral seizures in response to threshold stimulation. Vehicle-treated kindled rats that were then given topiramate displayed significantly attenuated behavioral seizures induced by the threshold stimulation.

CONCLUSIONS

Topiramate exhibited age-dependent disease-modifying effects under conditions of rapid kindling, but failed to block epileptogenesis. Topiramate also inhibited kindled seizures with equal efficacy across the three ages.

摘要

目的

研究托吡酯在不同发育阶段快速点燃条件下的抗癫痫发生、疾病修饰及抗惊厥作用。

方法

在给予托吡酯(200mg/kg)前后,检测2周龄、3周龄和5周龄Wistar大鼠的后放电阈值(ADT)和持续时间(ADD)。动物接受快速点燃方案(60次10秒的串刺激,每5分钟给予双极20Hz方波脉冲)。比较托吡酯组和赋形剂处理的对照大鼠在行为和脑电图癫痫发作的进展以及方案后24小时对测试刺激的反应。此外,对先前仅在点燃前给予赋形剂的大鼠,随后给予托吡酯以检查对已建立的点燃癫痫发作的影响。

结果

在2周龄动物中,托吡酯既不影响基线后放电,也不影响点燃癫痫发作的进展。在3周龄大鼠中,托吡酯不改变基线后放电,但显著延迟了对重复刺激的全面运动性癫痫发作的发生。托吡酯治疗5周龄大鼠可提高基线ADT,缩短ADD,并延迟点燃癫痫发作的进展。在最后一次点燃刺激后24小时,所有年龄的动物均表现出ADT降低、ADD增加,并对阈值刺激产生行为性癫痫发作。先前给予赋形剂的点燃大鼠随后给予托吡酯后,其由阈值刺激诱导的行为性癫痫发作明显减轻。

结论

托吡酯在快速点燃条件下表现出年龄依赖性的疾病修饰作用,但未能阻断癫痫发生。托吡酯在三个年龄段对点燃癫痫发作的抑制效果相同。

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