Hamani Clement, Mello Luiz E A M
Department of Physiology, UNIFESP-EPM, R. Botucatu 862, 04023-062 São Paulo-SP, Brazil.
Neurol Res. 2002 Mar;24(2):199-209. doi: 10.1179/016164102101199611.
In a recent publication, we have shown a potent interaction between the cholinergic and GABAergic systems in regard to seizure generation and developed the pilocarpine(pilo)/picrotoxin(PTX) model, in which combined injections of these agents have induced status epilepticus (SE) in rats. Here we report on the chronic features of this new animal model of epilepsy. Adult male Wistar rats were systemically injected with solutions containing 150/0.5 mg kg-1, 75/1.5 mg kg-1 and 50/2.0 mg kg-1 (pilo dose/PTX dose). Six epileptic and six control animals were observed for 120-131 days for the occurrence of spontaneous recurrent seizures (SRS). Electroencephalographic, neuropathologic and behavioral analyses were subsequently performed. Following SE, the animals went through a latent period and, subsequently, towards a state of 'chronic' epilepsy, characterized by the emergence of SRS. Animals that received 150/0.5 mg kg-1 presented a relatively short latent period, partial events as their most common initial seizure manifestations and a considerable subsequent progression towards generalization. The group injected with 75/1.5 mg kg-1 presented an extensive period during which the majority of the animals exclusively developed partial seizures (50 days). Animals injected with 50/2.0 mg kg-1 presented an average latent period of over 100 days. Only few animals within this group developed SRS. Our EEG, neuropathological and ictal behavioral findings, in conjunction with the fact that SE was required for the posterior development of SRS, suggest that our model parallels a human TLE condition. Even though diverse TLE models have been described, the pilo/PTX model has as a major feature the intriguing occurrence of disparities among these three groups in the chronic period, although no differences could be observed during SE induction. Future experiments conducted in this sense, might lead to important results in regard to the elucidation of mechanisms of epileptogenesis.
在最近发表的一篇文章中,我们展示了胆碱能系统和GABA能系统在癫痫发作产生方面的强大相互作用,并建立了毛果芸香碱(匹鲁卡品,pilo)/印防己毒素(PTX)模型,在该模型中联合注射这两种药物可诱发大鼠癫痫持续状态(SE)。在此,我们报告这种新型癫痫动物模型的慢性特征。成年雄性Wistar大鼠被全身注射含有150/0.5 mg kg-1、75/1.5 mg kg-1和50/2.0 mg kg-1(匹鲁卡品剂量/印防己毒素剂量)的溶液。观察6只癫痫大鼠和6只对照大鼠120 - 131天,记录自发性反复癫痫发作(SRS)的发生情况。随后进行脑电图、神经病理学和行为学分析。SE发作后,动物经历一个潜伏期,随后进入“慢性”癫痫状态,其特征为SRS的出现。接受150/0.5 mg kg-1剂量的动物潜伏期相对较短,最初发作表现以部分性发作最为常见,随后有相当比例进展为全身性发作。注射75/1.5 mg kg-1剂量组的动物在较长一段时间内(50天)大多数仅出现部分性发作。注射50/2.0 mg kg-1剂量组的动物平均潜伏期超过100天。该组中只有少数动物出现SRS。我们的脑电图、神经病理学和发作期行为学研究结果,以及SRS的后续发展需要SE这一事实,表明我们的模型与人类颞叶癫痫(TLE)情况相似。尽管已经描述了多种TLE模型,但匹鲁卡品/印防己毒素模型的一个主要特点是,这三组在慢性期出现了有趣的差异,尽管在诱导SE期间未观察到差异。从这个意义上进行的未来实验,可能会在阐明癫痫发生机制方面取得重要成果。