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Review: Cav2.3 R-type Voltage-Gated Ca2+ Channels - Functional Implications in Convulsive and Non-convulsive Seizure Activity

机译:评论:Cav2.3 R型电压门控Ca2 +通道-惊厥性和非惊厥性癫痫发作活动的功能含义

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Background:Researchers have gained substantial insight into mechanisms of synaptic transmission, hyperexcitability, excitotoxicity and neurodegeneration within the last decades. Voltage-gated Ca2+ channels are of central relevance in these processes. In particular, they are key elements in the etiopathogenesis of numerous seizure types and epilepsies. Earlier studies predominantly targeted on Cav2.1 P/Q-type and Cav3.2 T-type Ca2+ channels relevant for absence epileptogenesis. Recent findings bring other channels entities more into focus such as the Cav2.3 R-type Ca2+ channel which exhibits an intriguing role in ictogenesis and seizure propagation. Cav2.3 R-type voltage gated Ca2+ channels (VGCC) emerged to be important factors in the pathogenesis of absence epilepsy, human juvenile myoclonic epilepsy (JME), and cellular epileptiform activity, e.g. in CA1 neurons. They also serve as potential target for various antiepileptic drugs, such as lamotrigine and topiramate.
机译:背景:研究人员在过去几十年中对突触传递,过度兴奋,兴奋性毒性和神经退行性变的机理有了深刻的了解。电压门控Ca2 +通道在这些过程中具有重要意义。特别地,它们是许多癫痫发作类型和癫痫病因中的关键因素。较早的研究主要针对与缺乏癫痫发生有关的Cav2.1 P / Q型和Cav3.2 T型Ca2 +通道。最近的发现使其他通道实体变得更加受关注,例如Cav2.3 R型Ca2 +通道,在信息生成和癫痫发作传播中表现出令人着迷的作用。 Cav2.3 R型电压门控的Ca2 +通道(VGCC)成为了失神癫痫,人类青少年肌阵挛性癫痫(JME)和细胞癫痫样活动例如在CA1神经元中。它们还可以作为各种抗癫痫药的潜在靶标,例如拉莫三嗪和托吡酯。

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