Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain

Detalhes bibliográficos
Autor(a) principal: Fernandes, Anabela Silva
Data de Publicação: 2010
Outros Autores: Sousa, Nuno, Oliveira, Pedro, Maciel, P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/29577
Resumo: The FVB/N mouse strain (Mus musculus) is often used for generation of transgenic animals. However, it has also been the object of several studies in epilepsy research due to its increased susceptibility to develop spontaneous and induced seizures and its sensitivity to seizure-triggered neuronal death. We aimed to analyse behavioural changes observed in FVB/N mice that had seizure episodes throughout life. For this, we assessed the behaviour profile of 52-week old FVB/N animals displaying repeated spontaneous seizures, using the SHIRPA protocol. These epileptic mice also displayed a marked gait ataxia and decreased locomotor and exploratory activity. Moreover, these animals weighed less than control mice, and displayed increased signs of aggression and vocalization behaviours. Analysis of the data by clusters showed that in the epileptic mice there were significant deficits in the SHIRPA “spinocerebellar function”, “neuropsychiatric function” and “muscle and lower motor neuron function” scores, suggesting extensive brain damage caused by repeated experience of seizures.
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spelling Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strainScience & TechnologyThe FVB/N mouse strain (Mus musculus) is often used for generation of transgenic animals. However, it has also been the object of several studies in epilepsy research due to its increased susceptibility to develop spontaneous and induced seizures and its sensitivity to seizure-triggered neuronal death. We aimed to analyse behavioural changes observed in FVB/N mice that had seizure episodes throughout life. For this, we assessed the behaviour profile of 52-week old FVB/N animals displaying repeated spontaneous seizures, using the SHIRPA protocol. These epileptic mice also displayed a marked gait ataxia and decreased locomotor and exploratory activity. Moreover, these animals weighed less than control mice, and displayed increased signs of aggression and vocalization behaviours. Analysis of the data by clusters showed that in the epileptic mice there were significant deficits in the SHIRPA “spinocerebellar function”, “neuropsychiatric function” and “muscle and lower motor neuron function” scores, suggesting extensive brain damage caused by repeated experience of seizures.Anabela Silva Fernandes is the recipient of a scholarship from FCT (SFRH/BD/15910/2005).Scandinavian Society for Laboratory Animal Science (Scand-LAS)Universidade do MinhoFernandes, Anabela SilvaSousa, NunoOliveira, PedroMaciel, P.20102010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/29577eng0901-339310.23675/sjlas.v37i3.217http://sjlas.org/index.php/SJLAS/article/view/217info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:44:28Zoai:repositorium.sdum.uminho.pt:1822/29577Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:42:09.992452Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
title Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
spellingShingle Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
Fernandes, Anabela Silva
Science & Technology
title_short Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
title_full Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
title_fullStr Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
title_full_unstemmed Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
title_sort Motor and behavioural abnormalities associated with persistent spontaneous epilepsy in the fvb/n mouse strain
author Fernandes, Anabela Silva
author_facet Fernandes, Anabela Silva
Sousa, Nuno
Oliveira, Pedro
Maciel, P.
author_role author
author2 Sousa, Nuno
Oliveira, Pedro
Maciel, P.
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Fernandes, Anabela Silva
Sousa, Nuno
Oliveira, Pedro
Maciel, P.
dc.subject.por.fl_str_mv Science & Technology
topic Science & Technology
description The FVB/N mouse strain (Mus musculus) is often used for generation of transgenic animals. However, it has also been the object of several studies in epilepsy research due to its increased susceptibility to develop spontaneous and induced seizures and its sensitivity to seizure-triggered neuronal death. We aimed to analyse behavioural changes observed in FVB/N mice that had seizure episodes throughout life. For this, we assessed the behaviour profile of 52-week old FVB/N animals displaying repeated spontaneous seizures, using the SHIRPA protocol. These epileptic mice also displayed a marked gait ataxia and decreased locomotor and exploratory activity. Moreover, these animals weighed less than control mice, and displayed increased signs of aggression and vocalization behaviours. Analysis of the data by clusters showed that in the epileptic mice there were significant deficits in the SHIRPA “spinocerebellar function”, “neuropsychiatric function” and “muscle and lower motor neuron function” scores, suggesting extensive brain damage caused by repeated experience of seizures.
publishDate 2010
dc.date.none.fl_str_mv 2010
2010-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/29577
url http://hdl.handle.net/1822/29577
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0901-3393
10.23675/sjlas.v37i3.217
http://sjlas.org/index.php/SJLAS/article/view/217
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eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Scandinavian Society for Laboratory Animal Science (Scand-LAS)
publisher.none.fl_str_mv Scandinavian Society for Laboratory Animal Science (Scand-LAS)
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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