| Literature DB >> 29936231 |
Patricia G Saletti1, Idrish Ali2, Pablo M Casillas-Espinosa2, Bridgette D Semple2, Christos Panagiotis Lisgaras1, Solomon L Moshé3, Aristea S Galanopoulou4.
Abstract
Post-traumatic epilepsy (PTE) is diagnosed in 20% of individuals with acquired epilepsy, and can impact significantly the quality of life due to the seizures and other functional or cognitive and behavioral outcomes of the traumatic brain injury (TBI) and PTE. There is no available antiepileptogenic or disease modifying treatment for PTE. Animal models of TBI and PTE have been developed, offering useful insights on the value of inflammatory, neurodegenerative pathways, hemorrhages and iron accumulation, calcium channels and other target pathways that could be used for treatment development. Most of the existing preclinical studies test efficacy towards pathologies of functional recovery after TBI, while a few studies are emerging testing the effects towards induced or spontaneous seizures. Here we review the existing preclinical trials testing new candidate treatments for TBI sequelae and PTE, and discuss future directions for efforts aiming at developing antiepileptogenic and disease-modifying treatments.Entities:
Keywords: Antiepileptogenesis; Disease modification; Inflammation; Iron; Neurodegeneration; Outcomes; Preclinical trial; Tau; Traumatic brain injury
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Year: 2018 PMID: 29936231 PMCID: PMC6309524 DOI: 10.1016/j.nbd.2018.06.017
Source DB: PubMed Journal: Neurobiol Dis ISSN: 0969-9961 Impact factor: 5.996