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卡马西平和巴氯芬对4-氨基吡啶诱导的大鼠海马切片癫痫活动的影响。

Effects of carbamazepine and baclofen on 4-aminopyridine-induced epileptic activity in rat hippocampal slices.

作者信息

Watts A E, Jefferys J G

机构信息

Department of Physiology and Biophysics, St. Mary's Hospital Medical School, Imperial College, University of London.

出版信息

Br J Pharmacol. 1993 Mar;108(3):819-23. doi: 10.1111/j.1476-5381.1993.tb12884.x.

Abstract
  1. Rat transverse hippocampal slices exposed to 100 microM 4-aminopyridine (4-AP) generate spontaneous epileptic discharges ranging in duration from short 50 ms 'interictal' bursts to long 0.5-2 s 'polyspike' activity. 2. Here we compared the effects of the commonly used anticonvulsant, carbamazepine (40 microM) and the antispastic drug, baclofen (2 microM) on the various types of burst. 3. Carbamazepine completely abolished long bursts whilst leaving shorter bursts intact. This is consistent with its known anticonvulsant properties. 4. Baclofen greatly reduced the frequency of short bursts but did not block the long bursts. Rather, they became significantly more prolonged, indicating that baclofen does not have an anticonvulsant action, and may be proconvulsant. 5. These results conflict with conclusions based on studies using models that exhibited only interictal bursts, and emphasize the need to use experimental epilepsies which generate several types of epileptic discharge to evaluate the effects of putative anticonvulsant drugs. 6. The present findings suggest that GABAB receptors play a role in the transition of benign interictal bursts to longer polyspike activity which could develop into seizures in the whole animal.
摘要
  1. 暴露于100微摩尔4 - 氨基吡啶(4 - AP)的大鼠海马横切片会产生自发癫痫放电,其持续时间从短暂的50毫秒“发作间期”突发到长达0.5 - 2秒的“多棘波”活动不等。2. 在此,我们比较了常用抗惊厥药卡马西平(40微摩尔)和抗痉挛药巴氯芬(2微摩尔)对各种类型突发的影响。3. 卡马西平完全消除了长时间的突发,而使较短的突发保持不变。这与其已知的抗惊厥特性相符。4. 巴氯芬大大降低了短突发的频率,但并未阻断长突发。相反,长突发变得明显更持久,表明巴氯芬没有抗惊厥作用,可能具有促惊厥作用。5. 这些结果与基于仅表现出发作间期突发的模型研究得出的结论相冲突,并强调需要使用能产生多种类型癫痫放电的实验性癫痫模型来评估假定抗惊厥药物的效果。6. 目前的研究结果表明,GABAB受体在良性发作间期突发向更长的多棘波活动的转变中起作用,而这种多棘波活动在完整动物中可能发展为癫痫发作。

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