首页> 外文期刊>Epilepsy research >The novel antiepileptic drug carisbamate (RWJ 333369) is effective in inhibiting spontaneous recurrent seizure discharges and blocking sustained repetitive firing in cultured hippocampal neurons.
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The novel antiepileptic drug carisbamate (RWJ 333369) is effective in inhibiting spontaneous recurrent seizure discharges and blocking sustained repetitive firing in cultured hippocampal neurons.

机译:新型抗癫痫药carisbamate(RWJ 333369)可有效抑制培养的海马神经元自发性反复发作和阻止持续重复放电。

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This study was initiated to investigate effects of the novel neuromodulator carisbamate (RWJ 333369) in the hippocampal neuronal culture model of status epilepticus and spontaneous epileptiform discharges. Whole-cell current clamp techniques were used to determine the effects of carisbamate on spontaneous recurrent epileptiform discharges (SREDs, in vitro epilepsy), depolarization-induced sustained repetitive firing (SRF) and low Mg(2+)-induced continuous high frequency spiking (in vitro status epilepticus). This in vitro model is an important tool to study the effects of anticonvulsant drugs (AEDs) on SREDs that occur for the life of the neurons in culture. Carisbamate dose dependently blocked the expression and reoccurrence of SREDs. The ED(50) value for its antiepileptic effect was 58.75+/-2.43 microM. Inhibition of SRF is considered a common attribute of many AEDs. Carisbamate (100 microM) significantly decreased SRF in hippocampal neurons. All these effects of carisbamate were reversed during a 5 to 30 min drug washout period. When exposed to low Mg(2+) medium cultured hippocampal neurons exhibit high frequency spiking. This form of in vitro status epilepticus is not effectively blocked by conventional AEDs that are known to be effective in treating status epilepticus in humans. Carisbamate, like phenytoin and phenobarbital, had little or no effect on low Mg(2+)-induced continuous high frequency spiking. These results characterize the effects of carisbamate in the hippocampal neuronal culture model of epileptiform discharges and suggest that the ability of carisbamate to inhibit depolarization-induced SRF may account in part for some of it's anticonvulsant effect.
机译:这项研究的发起是为了研究新型神经调节剂氨基甲酸氨基甲酸酯(RWJ 333369)在癫痫持续状态和自发癫痫样放电海马神经元培养模型中的作用。全细胞电流钳技术用于确定氨基甲酸酯对自发性复发性癫痫样放电(SRED,体外癫痫),去极化诱导的持续重复放电(SRF)和低Mg(2+)诱导的持续高频突跳的影响(体外癫痫持续状态)。此体外模型是研究抗惊厥药物(AED)对在培养的神经元生命中发生的SRED的影响的重要工具。 Carisbamate剂量依赖性地阻断了SRED的表达和复发。 ED(50)的抗癫痫作用值为58.75 +/- 2.43 microM。抑制SRF被认为是许多AED的共同属性。 Carisbamate(100 microM)明显降低海马神经元的SRF。在5至30分钟的药物冲洗期间,卡里斯巴酯的所有这些作用都被逆转。当暴露于低Mg(2+)培养基时,培养的海马神经元表现出高频率的峰值。常规的体外抗癫痫药不能有效地阻断这种形式的体外癫痫持续状态,已知的传统抗癫痫药可有效治疗人的癫痫持续状态。 Carisbamate,像苯妥英钠和苯巴比妥,对低Mg(2+)引起的连续高频突波几乎没有影响。这些结果表征了氨基甲酸酯在癫痫样放电的海马神经元培养模型中的作用,并表明氨基甲酸酯抑制去极化诱导的SRF的能力可能部分解释了其抗惊厥作用。

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