在模拟人类颞叶癫痫的两种经典的动物模型-电刺激点燃(Kindling Model)和匹罗卡品诱导癫痫(Pilocarpine Model)的大鼠模型中,分别给大鼠NMDA受体非选择性抑..
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To try to identify the critical structures during epileptogenesis, we used the lithium-pilocarpine model that reproduces most clinical and neuropathological features of temporal lobe epilepsy (TLE).
为了尝试辨明癫痫发生的关键结构，我们使用锂-匹罗卡品模型，其能再现颞叶癫痫大多数的临床和病理特点。
The lithium-pilocarpine induced SE was used as the SE model.
建立氯化锂-匹罗卡品大鼠SE模型。
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