Disciplina de Neurociência, Departamento de Neurologia/Neurocirurgia, Escola Paulista de Medicina/Universidade Federal de São Paulo (EPM/UNIFESP), São Paulo, 04039-032, Brazil.
Posgrado de Neurología, Facultad de Ciencias Médicas, Universidad Nacional Autónoma de Honduras, Tegucigalpa, Honduras.
Sci Rep. 2021 Aug 18;11(1):16780. doi: 10.1038/s41598-021-96235-5.
There are no clinical interventions to prevent post-injury epilepsy, a common and devastating outcome after brain insults. Epileptogenic events that run from brain injury to epilepsy are poorly understood. Previous studies in our laboratory suggested Proechimys, an exotic Amazonian rodent, as resistant to acquired epilepsy development in post-status epilepticus models. The present comparative study was conducted to assess (1) stroke-related brain responses 24-h and 30 days after cortical photothrombosis and (2) post-stroke epilepsy between Proechimys rodents and Wistar rats, a traditional animal used for laboratory research. Proechimys group showed smaller volume of ischemic infarction and lesser glial activation than Wistar group. In contrast to Wistar rats, post-stroke decreased levels of pro-inflammatory cytokines and increased levels of anti-inflammatory mediators and growth factors were found in Proechimys. Electrophysiological signaling changes assessed by cortical spreading depression, in vitro and in vivo, showed that Wistar's brain is most severely affected by stroke. Chronic electrocorticographic recordings showed that injury did not lead to epilepsy in Proechimys whereas 88% of the Wistar rats developed post-stroke epilepsy. Science gains insights from comparative studies on diverse species. Proechimys rodents proved to be a useful animal model to study antiepileptogenic mechanisms after brain insults and complement conventional animal models.
目前尚无临床干预措施可预防脑损伤后的癫痫,这是脑损伤后的常见且具破坏性的后果。从脑损伤到癫痫的致痫事件尚不清楚。我们实验室的先前研究表明,外来的亚马逊河滨鼠 Proechimys 不易发生癫痫发作后状态的癫痫形成。本比较研究旨在评估:(1)皮质光血栓形成后 24 小时和 30 天的与中风相关的脑反应;(2)Proechimys 啮齿动物与 Wistar 大鼠(传统的实验室研究动物)之间的中风后癫痫。Proechimys 组的缺血性梗死体积小于 Wistar 组,神经胶质活化程度也较轻。与 Wistar 大鼠不同,Proechimys 中风后促炎细胞因子水平降低,抗炎介质和生长因子水平升高。皮质扩散性抑制的电生理信号变化的评估(在体外和体内)表明,Wistar 大鼠的大脑受中风影响最为严重。慢性皮层脑电图记录显示,损伤并未导致 Proechimys 发生癫痫,而 88%的 Wistar 大鼠发生了中风后癫痫。从不同物种的比较研究中获得科学见解。Proechimys 啮齿动物被证明是研究脑损伤后抗癫痫发生机制的有用动物模型,可补充传统的动物模型。