Proechimys guyannensis: An animal model of resistance to epilepsy

Bibliographic Details
Main Author: Arida, Ricardo Mario [UNIFESP]
Publication Date: 2005
Other Authors: Scorza, Fulvio Alexandre [UNIFESP], Carvalho, Reinaldo de Amorim, Cavalheiro, Esper Abrão [UNIFESP]
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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spelling 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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