Proechimys guyannensis: An animal model of resistance to epilepsy
Main Author: | |
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Publication Date: | 2005 |
Other Authors: | , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNIFESP |
Download full: | http://dx.doi.org/10.1111/j.1528-1167.2005.01065.x http://repositorio.unifesp.br/handle/11600/28062 |
Summary: | Purpose: the potential interest of Proechimys guyannensis (PG), a spiny rat species living in the Amazonian region, as an animal model of anticonvulsant mechanisms, prompted the investigation of the susceptibility of this animal species to different epileptogenic treatments.Methods: Adult male Wistar and PG animals were submitted to amygdala kindling, the pilocarpine model and the intrahippocampal kainic acid (KA) model. Electrographic, behavioral, and neuropathological changes were compared between Wistar and PG animals.Results: PG animals demonstrated a striking resistance to reaching stage 5 of kindling. of the 43 PG rats submitted to the kindling process, only three animals reached stage 5. in the pilocarpine and KA models, doses lower than those used in Wistar rats were able to induce status epilepticus (SE) in PG animals. Pilocarpine-induced SE in PG had a shorter duration, rarely exceeding 2 h, in contrast to the 8- to 12- h long SE in the Wistar rat. of the 61 PG animals injected with pilocarpine, 48 presented with SE and only two presented with some spontaneous seizures after silent periods of 60 and 66 days. KA elicited self-sustained electrographic SE in PG animals, which lasted for 72 h. None of the surviving animals presented with spontaneous seizures in the long-term observation period (up to 120 days).Conclusions: These findings indicate that the PG animal may have natural endogenous anticonvulsant mechanisms and also may be an animal model that is resistant to epileptogenic treatments. |
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Proechimys guyannensis: An animal model of resistance to epilepsyepilepsyProechimys guyannensiskindlingpilocarpinekainic acidPurpose: the potential interest of Proechimys guyannensis (PG), a spiny rat species living in the Amazonian region, as an animal model of anticonvulsant mechanisms, prompted the investigation of the susceptibility of this animal species to different epileptogenic treatments.Methods: Adult male Wistar and PG animals were submitted to amygdala kindling, the pilocarpine model and the intrahippocampal kainic acid (KA) model. Electrographic, behavioral, and neuropathological changes were compared between Wistar and PG animals.Results: PG animals demonstrated a striking resistance to reaching stage 5 of kindling. of the 43 PG rats submitted to the kindling process, only three animals reached stage 5. in the pilocarpine and KA models, doses lower than those used in Wistar rats were able to induce status epilepticus (SE) in PG animals. Pilocarpine-induced SE in PG had a shorter duration, rarely exceeding 2 h, in contrast to the 8- to 12- h long SE in the Wistar rat. of the 61 PG animals injected with pilocarpine, 48 presented with SE and only two presented with some spontaneous seizures after silent periods of 60 and 66 days. KA elicited self-sustained electrographic SE in PG animals, which lasted for 72 h. None of the surviving animals presented with spontaneous seizures in the long-term observation period (up to 120 days).Conclusions: These findings indicate that the PG animal may have natural endogenous anticonvulsant mechanisms and also may be an animal model that is resistant to epileptogenic treatments.Universidade Federal de São Paulo, Disciplina Neurol Expt, BR-04023900 São Paulo, BrazilUMC, Lab Neurociencias Nucl Pesquisas Tecnol, São Paulo, BrazilUniversidade Federal de São Paulo, Disciplina Neurol Expt, BR-04023900 São Paulo, BrazilWeb of ScienceWiley-BlackwellUniversidade Federal de São Paulo (UNIFESP)UMCArida, Ricardo Mario [UNIFESP]Scorza, Fulvio Alexandre [UNIFESP]Carvalho, Reinaldo de AmorimCavalheiro, Esper Abrão [UNIFESP]2016-01-24T12:37:32Z2016-01-24T12:37:32Z2005-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion189-197http://dx.doi.org/10.1111/j.1528-1167.2005.01065.xEpilepsia. Malden: Wiley-Blackwell, v. 46, p. 189-197, 2005.10.1111/j.1528-1167.2005.01065.x0013-9580http://repositorio.unifesp.br/handle/11600/28062WOS:000230499100032engEpilepsiainfo:eu-repo/semantics/openAccesshttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2023-05-18T13:33:26Zoai:repositorio.unifesp.br/:11600/28062Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652023-05-18T13:33:26Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Proechimys guyannensis: An animal model of resistance to epilepsy |
title |
Proechimys guyannensis: An animal model of resistance to epilepsy |
spellingShingle |
Proechimys guyannensis: An animal model of resistance to epilepsy Arida, Ricardo Mario [UNIFESP] epilepsy Proechimys guyannensis kindling pilocarpine kainic acid |
title_short |
Proechimys guyannensis: An animal model of resistance to epilepsy |
title_full |
Proechimys guyannensis: An animal model of resistance to epilepsy |
title_fullStr |
Proechimys guyannensis: An animal model of resistance to epilepsy |
title_full_unstemmed |
Proechimys guyannensis: An animal model of resistance to epilepsy |
title_sort |
Proechimys guyannensis: An animal model of resistance to epilepsy |
author |
Arida, Ricardo Mario [UNIFESP] |
author_facet |
Arida, Ricardo Mario [UNIFESP] Scorza, Fulvio Alexandre [UNIFESP] Carvalho, Reinaldo de Amorim Cavalheiro, Esper Abrão [UNIFESP] |
author_role |
author |
author2 |
Scorza, Fulvio Alexandre [UNIFESP] Carvalho, Reinaldo de Amorim Cavalheiro, Esper Abrão [UNIFESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) UMC |
dc.contributor.author.fl_str_mv |
Arida, Ricardo Mario [UNIFESP] Scorza, Fulvio Alexandre [UNIFESP] Carvalho, Reinaldo de Amorim Cavalheiro, Esper Abrão [UNIFESP] |
dc.subject.por.fl_str_mv |
epilepsy Proechimys guyannensis kindling pilocarpine kainic acid |
topic |
epilepsy Proechimys guyannensis kindling pilocarpine kainic acid |
description |
Purpose: the potential interest of Proechimys guyannensis (PG), a spiny rat species living in the Amazonian region, as an animal model of anticonvulsant mechanisms, prompted the investigation of the susceptibility of this animal species to different epileptogenic treatments.Methods: Adult male Wistar and PG animals were submitted to amygdala kindling, the pilocarpine model and the intrahippocampal kainic acid (KA) model. Electrographic, behavioral, and neuropathological changes were compared between Wistar and PG animals.Results: PG animals demonstrated a striking resistance to reaching stage 5 of kindling. of the 43 PG rats submitted to the kindling process, only three animals reached stage 5. in the pilocarpine and KA models, doses lower than those used in Wistar rats were able to induce status epilepticus (SE) in PG animals. Pilocarpine-induced SE in PG had a shorter duration, rarely exceeding 2 h, in contrast to the 8- to 12- h long SE in the Wistar rat. of the 61 PG animals injected with pilocarpine, 48 presented with SE and only two presented with some spontaneous seizures after silent periods of 60 and 66 days. KA elicited self-sustained electrographic SE in PG animals, which lasted for 72 h. None of the surviving animals presented with spontaneous seizures in the long-term observation period (up to 120 days).Conclusions: These findings indicate that the PG animal may have natural endogenous anticonvulsant mechanisms and also may be an animal model that is resistant to epileptogenic treatments. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-01-01 2016-01-24T12:37:32Z 2016-01-24T12:37:32Z |
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/10.1111/j.1528-1167.2005.01065.x Epilepsia. Malden: Wiley-Blackwell, v. 46, p. 189-197, 2005. 10.1111/j.1528-1167.2005.01065.x 0013-9580 http://repositorio.unifesp.br/handle/11600/28062 WOS:000230499100032 |
url |
http://dx.doi.org/10.1111/j.1528-1167.2005.01065.x http://repositorio.unifesp.br/handle/11600/28062 |
identifier_str_mv |
Epilepsia. Malden: Wiley-Blackwell, v. 46, p. 189-197, 2005. 10.1111/j.1528-1167.2005.01065.x 0013-9580 WOS:000230499100032 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Epilepsia |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://olabout.wiley.com/WileyCDA/Section/id-406071.html |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://olabout.wiley.com/WileyCDA/Section/id-406071.html |
dc.format.none.fl_str_mv |
189-197 |
dc.publisher.none.fl_str_mv |
Wiley-Blackwell |
publisher.none.fl_str_mv |
Wiley-Blackwell |
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 |
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1841453629235527680 |