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首页> 外文期刊>Epilepsy research >Anticonvulsant efficacy of gabapentin and levetiracetam in phenytoin-resistant kindled rats.
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Anticonvulsant efficacy of gabapentin and levetiracetam in phenytoin-resistant kindled rats.

机译:加巴喷丁和左乙拉西坦在耐苯妥英钠点燃的大鼠中的惊厥作用。

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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.
机译:我们评估了新的抗癫痫药(AED)加巴喷丁和左乙拉西坦在杏仁核点燃的大鼠中对苯妥英钠的反应的预选性。通过确定出院后阈值(ADT),即药物对局灶性癫痫发作作用的敏感措施,来测试抗惊厥反应。通过用苯妥英前药磷苯妥英钠反复试验,分离出三组点燃的大鼠:获得一致抗惊厥作用的大鼠(苯妥英钠应答剂),无抗惊厥反应的大鼠(苯妥英钠非应答剂)和反应可变的大鼠(苯妥英钠应答剂可变) )。后者最大的一组用于评估加巴喷丁和左乙拉西坦在腹膜后1小时对ADT产生显着的抗惊厥作用的剂量。药物管理。然后将有效剂量用于苯妥英钠应答者和非应答者中的药物测试。通过显着增加ADT,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。此外,两种药物在ADT电流下记录的癫痫发作严重程度均显着降低,表明这些药物影响癫痫病灶中的癫痫发作阈值,并在点燃模型中从病灶中发作。当确定除ADT外的继发性全身性癫痫发作(GST)阈值时,加巴喷丁和左乙拉西坦与药物前对照相比显着增加了该阈值。在苯妥英钠无反应者中,加巴喷丁和左乙拉西坦显着增加了ADT和GST,这与它们在较老的AED失败的难治性部分性癫痫患者中证明的疗效一致。在苯妥英钠应答者中,加巴喷丁在增加ADT和GST方面比未应答者更有效,证明这些点燃的大鼠组之间的差异扩展到其他AED。与加巴喷丁相反,左乙拉西坦在无反应者中增加ADT的效率比在反应者中更有效。这项研究的数据证实了苯妥英钠无反应者是寻找新的抗癫痫药的独特模型,该药具有改善难治性部分性癫痫的功效。

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