Prostaglandina E2 potencializa as convulsões induzidas por metilmalonato

Detalhes bibliográficos
Ano de defesa: 2009
Autor(a) principal: Salvadori, Mirian Graciela da Silva Stiebbe
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
BR
Farmacologia
UFSM
Programa de Pós-Graduação em Farmacologia
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: http://repositorio.ufsm.br/handle/1/8943
Resumo: Methylmalonic acidemias comprehend a group of innate error of the metabolism (EIM)characterized clinically and biochemically for the tissue accumulation of acid methylmalonic (MMA)and neurological dysfunction, including seizures. The clinical experience suggests that infections precipitate metabolic crises in methylmalonic acidemic patients. Since it has been demonstrated that MMA cause seizures, and that inflammation facilitates the occurrence of seizures in some animal models, is possible that inflammatory mediators, such as the prostaglandins, also facilitate MMAinduced seizures. Ciclooxigenase (COX) is the rate-limiting enzyme in the metabolic route by which the arachidonic acid is converted to prostaglandins. COX-2 is an isoform of cicloooxigenase that is induced at sites of injury / inflammation, and that is also constitutively expressed in some tissues, such as the central nervous system (CNS). It has been suggested that prostaglandin E2 (PGE2), the main product of COX-2 in the CNS, plays an important role in some neurodegenerative diseases, including epilepsy. However, no study has evaluated whether inflammatory mediators, such as the PGE2, facilitates MMA-induced seizures, to date. Thus, in this study we investigated the role of COX-2 and of PGE2 in seizures induced by MMA (2,5 µmol/2,5 µL, i.c.v.). While PGE2 (100 ng/2 μL, i.c.v.) facilitated, the selective COX-2 inhibitor celecoxib, attenuated MMA-induced seizures, assessed by electroencephalographic recordings in the hippocampus and cerebral cortex of rats. The ´protective effect of celecoxib against MMA-induced seizures was prevented by the PGE2. The results of this study support a facilitatory role for COX-2/PGE2 pathway in the MMA-induced seizures.