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加巴喷丁和左乙拉西坦在苯妥英耐药点燃大鼠中的抗惊厥疗效

Anticonvulsant efficacy of gabapentin and levetiracetam in phenytoin-resistant kindled rats.

作者信息

Löscher W, Reissmüller E, Ebert U

机构信息

Department of Pharmacology, School of Veterinary Medicine, Bünteweg 17, D-30559, Hannover, Germany.

出版信息

Epilepsy Res. 2000 Jun;40(1):63-77. doi: 10.1016/s0920-1211(00)00108-x.

Abstract

We evaluated the anticonvulsant efficacy of the new antiepileptic drugs (AEDs) gabapentin and levetiracetam in amygdala kindled rats that had been preselected with respect to their response to phenytoin. Anticonvulsant response was tested by determining the afterdischarge threshold (ADT), i.e. a sensitive measure for drug effects on focal seizure activity. By repeated testing with the phenytoin prodrug fosphenytoin, three groups of kindled rats were separated: rats in which consistent anticonvulsant effects were obtained (phenytoin responders), rats which showed no anticonvulsant response (phenytoin nonresponders), and rats with variable responses (variable phenytoin responders). The latter, largest group was used to evaluate at which doses gabapentin and levetiracetam exerted significant anticonvulsant effects on ADT 1 h after i.p. drug administration. Effective doses were then used for drug testing in phenytoin responders and nonresponders. Both gabapentin and levetiracetam proved to be effective anticonvulsant drugs in the kindling model by significantly increasing the ADT. In addition, both drugs markedly decreased seizure severity recorded at ADT currents, indicating that these drugs affect seizure threshold in the epileptic focus and seizure spread from the focus in the kindling model. When the threshold for secondary generalized seizures (GST) was determined in addition to ADT, gabapentin and levetiracetam strikingly increased this threshold compared to predrug control. In phenytoin nonresponders, gabapentin and levetiracetam significantly increased ADT and GST, which is in line with their proven efficacy in patients with refractory partial epilepsy in whom older AEDs have failed. In phenytoin responders, gabapentin tended to be more efficacious in increasing ADT and GST than in nonresponders, substantiating that the difference between these groups of kindled rats extends to other AEDs. In contrast to gabapentin, levetiracetam was more efficacious in increasing ADT in nonresponders than in responders. The data of this study substantiate that phenytoin nonresponders are a unique model for the search of new AEDs with improved efficacy in refractory partial epilepsy.

摘要

我们评估了新型抗癫痫药物(AEDs)加巴喷丁和左乙拉西坦对苯妥英钠反应预先筛选过的杏仁核点燃大鼠的抗惊厥疗效。通过测定放电后阈值(ADT)来测试抗惊厥反应,ADT是衡量药物对局灶性癫痫发作活动影响的一个敏感指标。通过用苯妥英前体药物磷苯妥英反复测试,将三组点燃大鼠区分开来:能获得持续抗惊厥效果的大鼠(苯妥英反应者)、无抗惊厥反应的大鼠(苯妥英无反应者)以及反应多变的大鼠(苯妥英反应多变者)。后者是数量最多的一组,用于评估腹腔注射药物1小时后加巴喷丁和左乙拉西坦在何种剂量下对ADT产生显著抗惊厥作用。然后将有效剂量用于苯妥英反应者和无反应者的药物测试。加巴喷丁和左乙拉西坦在点燃模型中均被证明是有效的抗惊厥药物,它们能显著提高ADT。此外,两种药物均显著降低了在ADT电流下记录的癫痫发作严重程度,这表明这些药物影响癫痫病灶中的癫痫发作阈值以及点燃模型中癫痫发作从病灶的扩散。除了ADT外,当测定继发性全身性癫痫发作(GST)阈值时,与给药前对照相比,加巴喷丁和左乙拉西坦显著提高了该阈值。在苯妥英无反应者中,加巴喷丁和左乙拉西坦显著提高了ADT和GST,这与它们在老年AEDs治疗无效的难治性部分性癫痫患者中已证实的疗效一致。在苯妥英反应者中,加巴喷丁在提高ADT和GST方面往往比无反应者更有效,这证实了这些点燃大鼠组之间的差异也延伸到其他AEDs。与加巴喷丁相反,左乙拉西坦在无反应者中提高ADT比在反应者中更有效。本研究数据证实,苯妥英无反应者是寻找在难治性部分性癫痫中疗效更佳的新型AEDs的独特模型。

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