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A Murine Model to Study Epilepsy and SUDEP Induced by Malaria Infection

One of the largest single sources of epilepsy in the world is produced as a neurological sequela in survivors of cerebral malaria. Nevertheless, the pathophysiological mechanisms of such epileptogenesis remain unknown and no adjunctive therapy during cerebral malaria has been shown to reduce the rat...

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Detalles Bibliográficos
Autores principales: Ssentongo, Paddy, Robuccio, Anna E., Thuku, Godfrey, Sim, Derek G., Nabi, Ali, Bahari, Fatemeh, Shanmugasundaram, Balaji, Billard, Myles W., Geronimo, Andrew, Short, Kurt W., Drew, Patrick J., Baccon, Jennifer, Weinstein, Steven L., Gilliam, Frank G., Stoute, José A., Chinchilli, Vernon M., Read, Andrew F., Gluckman, Bruce J., Schiff, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341121/
https://www.ncbi.nlm.nih.gov/pubmed/28272506
http://dx.doi.org/10.1038/srep43652
Descripción
Sumario:One of the largest single sources of epilepsy in the world is produced as a neurological sequela in survivors of cerebral malaria. Nevertheless, the pathophysiological mechanisms of such epileptogenesis remain unknown and no adjunctive therapy during cerebral malaria has been shown to reduce the rate of subsequent epilepsy. There is no existing animal model of postmalarial epilepsy. In this technical report we demonstrate the first such animal models. These models were created from multiple mouse and parasite strain combinations, so that the epilepsy observed retained universality with respect to genetic background. We also discovered spontaneous sudden unexpected death in epilepsy (SUDEP) in two of our strain combinations. These models offer a platform to enable new preclinical research into mechanisms and prevention of epilepsy and SUDEP.