C-Fos, Jun D and HSP72 immunoreactivity, and neuronal injury following lithium-pilocarpine induced status epilepticus in immature and adult rats

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dc.contributor.author Dube, C.
dc.contributor.author Andre, V
dc.contributor.author Covolan, Luciene [UNIFESP]
dc.contributor.author Ferrandon, A.
dc.contributor.author Marescaux, C.
dc.contributor.author Nehlig, A.
dc.date.accessioned 2016-01-24T12:30:43Z
dc.date.available 2016-01-24T12:30:43Z
dc.date.issued 1998-12-10
dc.identifier http://dx.doi.org/10.1016/S0169-328X(98)00282-4
dc.identifier.citation Molecular Brain Research. Amsterdam: Elsevier B.V., v. 63, n. 1, p. 139-154, 1998.
dc.identifier.issn 0169-328X
dc.identifier.uri http://repositorio.unifesp.br/handle/11600/25996
dc.description.abstract In order to follow the maturation-related evolution of neuronal damage, cellular activation and stress response subsequent to Li-Pilo seizures in the 10- (P10), 21-day-old (P21) and adult rat, we analyzed the expression of the c-Fos protein as a marker of cellular activation, HSP72 immunoreactivity as the stress response and silver staining for the assessment of neuronal damage in 20 selected brain regions. the early wave of c-Fos measured at 2 h after the onset of seizures was present in most structures of the animals at the three ages studied and particularly strong in the cerebral cortex, hippocampus and amygdala. the late wave of c-Fos measured at 24 h after the onset of seizures and that was shown to correlate to neuronal damage was absent from the P10 rat brain, and present mainly in the cerebral cortex and hippocampus of P21 and adult rats. the expression of the stress response, assessed by the immunoreactivity of HSP72 at 24 h after the seizures was absent from the P10 rat brain and present in the entorhinal cortex, amygdala, hippocampus and thalamus of P21 and adult rats. the expression of Jun D at 24 h after the seizures was discrete and present in most brain regions at all ages. Neuronal injury assessed by silver staining at 6 h after the onset of seizures was very discrete in the brain of the P10 rat and limited to a few neurons in the piriform and entorhinal cortices. in older animals, marked neuronal degeneration occurred in the cerebral cortex, amygdala, hippocampus, lateral septum and thalamus. Thus the immediate cell activation induced by lithium-pilocarpine seizures which is present at all ages translates only into a late wave of c-Fos and the expression of HSP72 in P21 and adult animals in which there will be extensive cell damage. (C) 1998 Elsevier Science B.V. All rights reserved. en
dc.format.extent 139-154
dc.language.iso eng
dc.publisher Elsevier B.V.
dc.relation.ispartof Molecular Brain Research
dc.rights Acesso restrito
dc.subject seizure en
dc.subject transcription factor en
dc.subject neuronal damage en
dc.subject development en
dc.title C-Fos, Jun D and HSP72 immunoreactivity, and neuronal injury following lithium-pilocarpine induced status epilepticus in immature and adult rats en
dc.type Artigo
dc.rights.license http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.contributor.institution Univ Strasbourg 1
dc.contributor.institution Universidade Federal de São Paulo (UNIFESP)
dc.description.affiliation Univ Strasbourg 1, Fac Med, INSERM, U398, F-67085 Strasbourg, France
dc.description.affiliation Escola Paulista Med, UNIFESP, Dept Fisiol, BR-04023 São Paulo, Brazil
dc.description.affiliationUnifesp Escola Paulista Med, UNIFESP, Dept Fisiol, BR-04023 São Paulo, Brazil
dc.identifier.doi 10.1016/S0169-328X(98)00282-4
dc.description.source Web of Science
dc.identifier.wos WOS:000077570500013



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