Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy

Bibliographic Details
Main Author: Covolan, Luciene [UNIFESP]
Publication Date: 2006
Other Authors: Mello, Luiz Eugenio Araujo de Moraes [UNIFESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNIFESP
dARK ID: ark:/48912/001300002kn27
Download full: http://dx.doi.org/10.1590/S0100-879X2006000700010
http://repositorio.unifesp.br/handle/11600/3146
Summary: Pilocarpine-induced (320 mg/kg, ip) status epilepticus (SE) in adult (2-3 months) male Wistar rats results in extensive neuronal damage in limbic structures. Here we investigated whether the induction of a second SE (N = 6) would generate damage and cell loss similar to that seen after a first SE (N = 9). Counts of silver-stained (indicative of cell damage) cells, using the Gallyas argyrophil III method, revealed a markedly lower neuronal injury in animals submitted to re-induction of SE compared to rats exposed to a single episode of pilocarpine-induced SE. This effect could be explained as follows: 1) the first SE removes the vulnerable cells, leaving behind resistant cells that are not affected by the second SE; 2) the first SE confers increased resistance to the remaining cells, analogous to the process of ischemic tolerance. Counting of Nissl-stained cells was performed to differentiate between these alternative mechanisms. Our data indicate that different neuronal populations react differently to SE induction. For some brain areas most, if not all, of the vulnerable cells are lost after an initial insult leaving only relatively resistant cells and little space for further damage or cell loss. For some other brain areas, in contrast, our data support the hypothesis that surviving cells might be modified by the initial insult which would confer a sort of excitotoxic tolerance. As a consequence of both mechanisms, subsequent insults after an initial insult result in very little damage regardless of their intensity.
id UFSP_b62f6dc8ec624d35bb86c9899d123ee3
oai_identifier_str oai:repositorio.unifesp.br:11600/3146
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsyCell injuryStatus epilepticusEpilepsyPilocarpineSpontaneous seizuresPilocarpine-induced (320 mg/kg, ip) status epilepticus (SE) in adult (2-3 months) male Wistar rats results in extensive neuronal damage in limbic structures. Here we investigated whether the induction of a second SE (N = 6) would generate damage and cell loss similar to that seen after a first SE (N = 9). Counts of silver-stained (indicative of cell damage) cells, using the Gallyas argyrophil III method, revealed a markedly lower neuronal injury in animals submitted to re-induction of SE compared to rats exposed to a single episode of pilocarpine-induced SE. This effect could be explained as follows: 1) the first SE removes the vulnerable cells, leaving behind resistant cells that are not affected by the second SE; 2) the first SE confers increased resistance to the remaining cells, analogous to the process of ischemic tolerance. Counting of Nissl-stained cells was performed to differentiate between these alternative mechanisms. Our data indicate that different neuronal populations react differently to SE induction. For some brain areas most, if not all, of the vulnerable cells are lost after an initial insult leaving only relatively resistant cells and little space for further damage or cell loss. For some other brain areas, in contrast, our data support the hypothesis that surviving cells might be modified by the initial insult which would confer a sort of excitotoxic tolerance. As a consequence of both mechanisms, subsequent insults after an initial insult result in very little damage regardless of their intensity.Universidade Federal de São Paulo (UNIFESP) Departamento de FisiologiaUNIFESP, Depto. de FisiologiaSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Covolan, Luciene [UNIFESP]Mello, Luiz Eugenio Araujo de Moraes [UNIFESP]2015-06-14T13:36:19Z2015-06-14T13:36:19Z2006-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion915-924application/pdfhttp://dx.doi.org/10.1590/S0100-879X2006000700010Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 39, n. 7, p. 915-924, 2006.10.1590/S0100-879X2006000700010S0100-879X2006000700010.pdf0100-879XS0100-879X2006000700010http://repositorio.unifesp.br/handle/11600/3146WOS:000239624200010ark:/48912/001300002kn27engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-05T23:19:53Zoai:repositorio.unifesp.br:11600/3146Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-05T23:19:53Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
title Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
spellingShingle Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
Covolan, Luciene [UNIFESP]
Cell injury
Status epilepticus
Epilepsy
Pilocarpine
Spontaneous seizures
title_short Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
title_full Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
title_fullStr Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
title_full_unstemmed Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
title_sort Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
author Covolan, Luciene [UNIFESP]
author_facet Covolan, Luciene [UNIFESP]
Mello, Luiz Eugenio Araujo de Moraes [UNIFESP]
author_role author
author2 Mello, Luiz Eugenio Araujo de Moraes [UNIFESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Covolan, Luciene [UNIFESP]
Mello, Luiz Eugenio Araujo de Moraes [UNIFESP]
dc.subject.por.fl_str_mv Cell injury
Status epilepticus
Epilepsy
Pilocarpine
Spontaneous seizures
topic Cell injury
Status epilepticus
Epilepsy
Pilocarpine
Spontaneous seizures
description Pilocarpine-induced (320 mg/kg, ip) status epilepticus (SE) in adult (2-3 months) male Wistar rats results in extensive neuronal damage in limbic structures. Here we investigated whether the induction of a second SE (N = 6) would generate damage and cell loss similar to that seen after a first SE (N = 9). Counts of silver-stained (indicative of cell damage) cells, using the Gallyas argyrophil III method, revealed a markedly lower neuronal injury in animals submitted to re-induction of SE compared to rats exposed to a single episode of pilocarpine-induced SE. This effect could be explained as follows: 1) the first SE removes the vulnerable cells, leaving behind resistant cells that are not affected by the second SE; 2) the first SE confers increased resistance to the remaining cells, analogous to the process of ischemic tolerance. Counting of Nissl-stained cells was performed to differentiate between these alternative mechanisms. Our data indicate that different neuronal populations react differently to SE induction. For some brain areas most, if not all, of the vulnerable cells are lost after an initial insult leaving only relatively resistant cells and little space for further damage or cell loss. For some other brain areas, in contrast, our data support the hypothesis that surviving cells might be modified by the initial insult which would confer a sort of excitotoxic tolerance. As a consequence of both mechanisms, subsequent insults after an initial insult result in very little damage regardless of their intensity.
publishDate 2006
dc.date.none.fl_str_mv 2006-07-01
2015-06-14T13:36:19Z
2015-06-14T13:36:19Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0100-879X2006000700010
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 39, n. 7, p. 915-924, 2006.
10.1590/S0100-879X2006000700010
S0100-879X2006000700010.pdf
0100-879X
S0100-879X2006000700010
http://repositorio.unifesp.br/handle/11600/3146
WOS:000239624200010
dc.identifier.dark.fl_str_mv ark:/48912/001300002kn27
url http://dx.doi.org/10.1590/S0100-879X2006000700010
http://repositorio.unifesp.br/handle/11600/3146
identifier_str_mv Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 39, n. 7, p. 915-924, 2006.
10.1590/S0100-879X2006000700010
S0100-879X2006000700010.pdf
0100-879X
S0100-879X2006000700010
WOS:000239624200010
ark:/48912/001300002kn27
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brazilian Journal of Medical and Biological Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 915-924
application/pdf
dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
_version_ 1848497799588478976