Departamento de Fisiologia, Universidade Federal de São Paulo, São Paulo, SP, Brasil.
Associação Brasileira de Epilepsia, São Paulo, SP, Brasil.
Braz J Med Biol Res. 2020 Dec 18;54(2):e10656. doi: 10.1590/1414-431X202010656. eCollection 2020.
Research on the prevention of post-traumatic epilepsy (PTE) has seen remarkable advances regarding its physiopathology in recent years. From the search for biomarkers that might be used to indicate individual susceptibility to the development of new animal models and the investigation of new drugs, a great deal of knowledge has been amassed. Various groups have concentrated efforts in generating new animal models of traumatic brain injury (TBI) in an attempt to provide the means to further produce knowledge on the subject. Here we forward the hypothesis that restricting the search of biomarkers and of new drugs to prevent PTE by using only a limited set of TBI models might hamper the understanding of this relevant and yet not preventable medical condition.
近年来,针对创伤后癫痫(PTE)的预防机制的研究在生理学和病理学方面取得了显著的进展。从寻找可能用于指示个体易感性的生物标志物,到新动物模型的建立和新药物的研究,人们已经积累了大量的知识。各个研究小组致力于建立新的创伤性脑损伤(TBI)动物模型,以进一步探索相关知识,这是一个重要的尝试。在这里,我们提出了一个假设,即如果仅使用有限数量的 TBI 模型来限制预防 PTE 的生物标志物和新药的研究,可能会阻碍对这一相关且不可预防的医学病症的理解。