Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1111/ner.12688 https://repositorio.unifesp.br/handle/11600/54214 |
Resumo: | Introduction and ObjectivesCognitive impairment is a significant comorbidity of temporal lobe epilepsy that is associated with extensive hippocampal cell loss. Deep brain stimulation (DBS) of the anterior thalamic nucleus (ANT) has been used for the treatment of refractory partial seizures. In the pilocarpine model of epilepsy, ANT DBS applied during status epilepticus (SE) reduces hippocampal inflammation and apoptosis. When given to chronic epileptic animals it reduces hippocampal excitability and seizure frequency. Here, we tested whether ANT DBS delivered during SE and the silent phase of the pilocarpine model would reduce cognitive impairment when animals became chronically epileptic. Materials and MethodsSE was induced by a systemic pilocarpine injection (320 mg/kg). Immediately after SE onset, rats were assigned to receive DBS during the first six hours of SE (n=8 |
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Repositório Institucional da UNIFESP |
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Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsydeep brain stimulationhippocampuslearningneuroprotectionpilocarpinethalamuswater mazeIntroduction and ObjectivesCognitive impairment is a significant comorbidity of temporal lobe epilepsy that is associated with extensive hippocampal cell loss. Deep brain stimulation (DBS) of the anterior thalamic nucleus (ANT) has been used for the treatment of refractory partial seizures. In the pilocarpine model of epilepsy, ANT DBS applied during status epilepticus (SE) reduces hippocampal inflammation and apoptosis. When given to chronic epileptic animals it reduces hippocampal excitability and seizure frequency. Here, we tested whether ANT DBS delivered during SE and the silent phase of the pilocarpine model would reduce cognitive impairment when animals became chronically epileptic. Materials and MethodsSE was induced by a systemic pilocarpine injection (320 mg/kg). Immediately after SE onset, rats were assigned to receive DBS during the first six hours of SE (n=8DBSa group) or during SE+the silent period (i.e., 6 h/day until the animals developed the first spontaneous recurrent seizuren=10DBSs group). Four months following SE, animals underwent water maze testing and histological evaluation. Nonstimulated chronic epileptic animals (n=13PCTL group) and age-matched naive rats (n=11, CTL group) were used as controls. Results were analyzed by repeated-measures analyses of variance (RM_ANOVA) and one-way ANOVAs, followed by Newman-Keuls post hoc tests. ResultsAlthough all groups learned the spatial task, epileptic animals with or without DBS spent significantly less time in the platform quadrant, denoting a spatial memory deficit (p<0.02). Despite these negative behavioral results, we found that animals given DBS had a significantly higher number of cells in the CA1 region and dentate gyrus. Mossy fiber sprouting was similar among all epileptic groups. ConclusionsDespite lesser hippocampal neuronal loss, ANT DBS delivered either during SE or during SE and the silent phase of the pilocarpine model did not mitigate memory deficits in chronic epileptic rats.Univ Fed Sao Paulo, Dept Fisiol, Rua Botucatu 862, BR-04023062 Sao Paulo, SP, BrazilCtr Addict & Mental Hlth, Behav Neurobiol Lab, Toronto, ON, CanadaUniv Toronto, Toronto Western Hosp, Div Neurosurg, Toronto, ON, CanadaUniv Fed Sao Paulo, Dept Fisiol, Rua Botucatu 862, BR-04023062 Sao Paulo, SP, BrazilWeb of ScienceFAPESPCNPqCAPESFAPESP [2012/50950-2]CNPq [304021/2015-6]CAPESWiley2020-07-08T13:09:48Z2020-07-08T13:09:48Z2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion160-167http://dx.doi.org/10.1111/ner.12688Neuromodulation. Hoboken, v. 21, n. 2, p. 160-167, 2018.10.1111/ner.126881094-7159https://repositorio.unifesp.br/handle/11600/54214WOS:000424282700006engNeuromodulationHobokeninfo:eu-repo/semantics/openAccessFerreira, Elenn Soares [UNIFESP]Vieira, Lais Gabrielle [UNIFESP]Moraes, Daniela Macedo [UNIFESP]Amorim, Beatriz O. [UNIFESP]Malheiros, Jackeline Moraes [UNIFESP]Hamani, ClementCovolan, Luciene [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2021-09-30T17:31:41Zoai:repositorio.unifesp.br/:11600/54214Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652021-09-30T17:31:41Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy |
title |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy |
spellingShingle |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy Ferreira, Elenn Soares [UNIFESP] deep brain stimulation hippocampus learning neuroprotection pilocarpine thalamus water maze |
title_short |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy |
title_full |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy |
title_fullStr |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy |
title_full_unstemmed |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy |
title_sort |
Long-Term Effects of Anterior Thalamic Nucleus Deep Brain Stimulation on Spatial Learning in the Pilocarpine Model of Temporal Lobe Epilepsy |
author |
Ferreira, Elenn Soares [UNIFESP] |
author_facet |
Ferreira, Elenn Soares [UNIFESP] Vieira, Lais Gabrielle [UNIFESP] Moraes, Daniela Macedo [UNIFESP] Amorim, Beatriz O. [UNIFESP] Malheiros, Jackeline Moraes [UNIFESP] Hamani, Clement Covolan, Luciene [UNIFESP] |
author_role |
author |
author2 |
Vieira, Lais Gabrielle [UNIFESP] Moraes, Daniela Macedo [UNIFESP] Amorim, Beatriz O. [UNIFESP] Malheiros, Jackeline Moraes [UNIFESP] Hamani, Clement Covolan, Luciene [UNIFESP] |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Ferreira, Elenn Soares [UNIFESP] Vieira, Lais Gabrielle [UNIFESP] Moraes, Daniela Macedo [UNIFESP] Amorim, Beatriz O. [UNIFESP] Malheiros, Jackeline Moraes [UNIFESP] Hamani, Clement Covolan, Luciene [UNIFESP] |
dc.subject.por.fl_str_mv |
deep brain stimulation hippocampus learning neuroprotection pilocarpine thalamus water maze |
topic |
deep brain stimulation hippocampus learning neuroprotection pilocarpine thalamus water maze |
description |
Introduction and ObjectivesCognitive impairment is a significant comorbidity of temporal lobe epilepsy that is associated with extensive hippocampal cell loss. Deep brain stimulation (DBS) of the anterior thalamic nucleus (ANT) has been used for the treatment of refractory partial seizures. In the pilocarpine model of epilepsy, ANT DBS applied during status epilepticus (SE) reduces hippocampal inflammation and apoptosis. When given to chronic epileptic animals it reduces hippocampal excitability and seizure frequency. Here, we tested whether ANT DBS delivered during SE and the silent phase of the pilocarpine model would reduce cognitive impairment when animals became chronically epileptic. Materials and MethodsSE was induced by a systemic pilocarpine injection (320 mg/kg). Immediately after SE onset, rats were assigned to receive DBS during the first six hours of SE (n=8 |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018 2020-07-08T13:09:48Z 2020-07-08T13:09:48Z |
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/ner.12688 Neuromodulation. Hoboken, v. 21, n. 2, p. 160-167, 2018. 10.1111/ner.12688 1094-7159 https://repositorio.unifesp.br/handle/11600/54214 WOS:000424282700006 |
url |
http://dx.doi.org/10.1111/ner.12688 https://repositorio.unifesp.br/handle/11600/54214 |
identifier_str_mv |
Neuromodulation. Hoboken, v. 21, n. 2, p. 160-167, 2018. 10.1111/ner.12688 1094-7159 WOS:000424282700006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Neuromodulation |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
160-167 |
dc.coverage.none.fl_str_mv |
Hoboken |
dc.publisher.none.fl_str_mv |
Wiley |
publisher.none.fl_str_mv |
Wiley |
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_ |
1814268302092926976 |