Assessment of the progressive nature of cell damage in the pilocarpine model of epilepsy
| Main Author: | |
|---|---|
| Publication Date: | 2006 |
| Other Authors: | |
| 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. |
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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 |
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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 |
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ark:/48912/001300002kn27 |
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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 |
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eng |
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Brazilian Journal of Medical and Biological Research |
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info:eu-repo/semantics/openAccess |
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openAccess |
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915-924 application/pdf |
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Associação Brasileira de Divulgação Científica |
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Associação Brasileira de Divulgação Científica |
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reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
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Universidade Federal de São Paulo (UNIFESP) |
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UNIFESP |
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Repositório Institucional da UNIFESP |
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Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
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biblioteca.csp@unifesp.br |
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1848497799588478976 |