Envolvimento das proteínas fosforiladas no resíduo de tirosina no hipocampo de ratos submetidos ao status epilepticus induzido por pilocarpina

Detalhes bibliográficos
Ano de defesa: 2016
Autor(a) principal: Castro Neto, Eduardo Ferreira de [UNIFESP]
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de São Paulo (UNIFESP)
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=3635061
http://repositorio.unifesp.br/handle/11600/46763
Resumo: Protein phosphorylation on tyrosine residue has been associated with different pathologies in the nervous system, including temporal lobe epilepsy. Objective: The objective of this work was to identify the phosphotyrosine proteins involved in status epilepticus (SE) onset/maintenance and those linked to SE resistance in animals submitted to pilocarpine-induced epilepsy. Method: Three groups of animals were studied: SE Group (rats with 5 h of SE, n-=5); PSS group (pilocarpine-injected animals that did not develop SE, n=5) and Control Group (saline-treated rats, n=5). The hippocampi were isolated and submitted to proarray kit, (Full Moon BioSystems, Inc.) containing specific antibodies to identify 228 phosphoproteins. Data were analyzed using ANOVA and Tukey- Kramer as post-test and p ? 0.05 was accepted. Results: One hundred twenty three out of 228 phosphoproteins presented significant altered levels among groups. From these 123 phosphoproteins, 36 attracted our attention due to their important particularities, that is, 18 presented increased phosphorylation compared to control and non-SE groups, 12 from non-SE group displayed significant differences when compared to control and SE groups and 6 presented altered levels among all groups. Conclusion: In this study we identified proteins that are probably linked to the generation of SE from those linked to the SE resistance. Knowing pathways involved in epileptogenesis may help to understand the mechanisms responsible for different vulnerabilities to long-lasting seizures.