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癫痫持续状态后的癫痫发生反映了年龄和模型依赖性可塑性。

Epileptogenesis after status epilepticus reflects age- and model-dependent plasticity.

作者信息

Sankar R, Shin D, Mazarati A M, Liu H, Katsumori H, Lezama R, Wasterlain C G

机构信息

Department of Neurology, University of California at Los Angeles School of Medicine, 90095-1752, USA.

出版信息

Ann Neurol. 2000 Oct;48(4):580-9.

PMID:11026441
Abstract

Although epilepsy often begins in childhood, factors that contribute to the development of epilepsy as a consequence of status epilepticus (SE) during early development are poorly understood. We investigated animal models in which seizure-induced epileptogenicity could be studied. Rats undergoing self-sustaining SE induced by perforant path stimulation (PPS) at the ages of postnatal day 21 (P21) and P35 were compared with those subjected to SE by lithium and pilocarpine (LiPC). Although only one animal subjected to PPS at P21 developed chronic spontaneous seizures by several months of observation, all the animals subjected to PPS at P35 became epileptic. In the LiPC model, however, most of the rat pups subjected to SE at P21 became epileptic. Animals with spontaneous seizures showed increased inhibition in the dentate gyrus, a characteristic of the epileptic brain, with evidence of mossy fiber synaptic reorganization. Examination of circuit recruitment by c-Jun immunohistochemistry showed activation restricted to the hippocampus in P21 animals subjected to PPS, although extensive activation of hippocampal and extrahippocampal structures was seen in pups subjected to PPS-induced self-sustaining SE at P35 or LiPC SE at P21. These results demonstrate that the appearance of epilepsy as a consequence of SE is influenced by the type of insult as well as by age-dependent circuit recruitment.

摘要

尽管癫痫常始于儿童期,但对于早期发育过程中因癫痫持续状态(SE)导致癫痫发生的相关因素,我们却知之甚少。我们研究了可用于研究癫痫发作诱导的致痫性的动物模型。将出生后第21天(P21)和P35时经穿通通路刺激(PPS)诱导发生自我持续性SE的大鼠,与经锂盐和匹鲁卡品(LiPC)诱导发生SE的大鼠进行比较。尽管在长达数月的观察期内,仅1只在P21时接受PPS刺激的动物出现了慢性自发性癫痫发作,但所有在P35时接受PPS刺激的动物均发生了癫痫。然而,在LiPC模型中,大多数在P21时接受SE刺激的幼鼠都发生了癫痫。出现自发性癫痫发作的动物在齿状回表现出抑制增强,这是癫痫脑的一个特征,同时伴有苔藓纤维突触重组的证据。通过c-Jun免疫组化检测回路募集情况发现,在P21时接受PPS刺激的动物中,激活仅限于海马体,而在P35时接受PPS诱导的自我持续性SE或在P21时接受LiPC诱导的SE的幼鼠中,则可见海马体和海马体外结构的广泛激活。这些结果表明,SE导致的癫痫出现受损伤类型以及年龄依赖性回路募集的影响。

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Epileptogenesis after status epilepticus reflects age- and model-dependent plasticity.癫痫持续状态后的癫痫发生反映了年龄和模型依赖性可塑性。
Ann Neurol. 2000 Oct;48(4):580-9.
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