Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study

Detalhes bibliográficos
Autor(a) principal: Santos, N. F.
Data de Publicação: 2000
Outros Autores: Marques, R. H., Correia, L., Sinigaglia-Coimbra, Rita [UNIFESP], Calderazzo, Lineu [UNIFESP], Sanabria, ERG, Cavalheiro, Esper Abrão [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1111/j.1528-1157.2000.tb01558.x
http://repositorio.unifesp.br/handle/11600/26206
Resumo: Purpose: Animal models are useful for the study of status epilepticus (SE)-induced epileptogenesis and neurological sequelae, especially during early brain development. Here. we show several permanent abnormalities in animals subjected to multiple SE during early development.Methods: Wistar pup rats (7 to 9 days old) were subjected to three consecutive episodes of SE induced by systemic pilocarpine injections. To study the long-lasting consequences of early-induced SE, chronic electroencephalographic recordings were made from the hippocampus and cortex and several behavioral tests (inhibitory step-down avoidance, rota-rod, open field, elevated plus-maze, and Skinner box) were performed at postnatal days 30 to 90. We also investigated in vitro electrophysiological responses of the CA1 area using extracellular recordings in hippocampal slices. A histological analysis was done using cresyl violet staining 24 hours and several months after SE induction. Apoptotic cell death was evaluated by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL staining) 24 hours after the last SE episode.Results: Electloencephalographic recordings from 30- to 90-day-old rats that had been subjected to multiple SE episodes in early life showed marked changes compared with those from nontreated controls. These included frequent episodes of continuous complex spiking activity and high-voltage ictal discharges, with a small percentage of these rats presenting spontaneous behavioral seizures. These animals also presented evidence of severe cognitive deficit in adulthood. in vitro, a persistent hyperexcitability of the CAI area was detected in experimental animals. Histological analysis of the brains did not reveal any major long-term pathological changes. Nevertheless, an increased number of TUNEL-positive nuclei were present in some animals in both the hippocampus and the thalamus.Conclusions: These data show persistent abnormalities in animals subjected to multiple SE episodes during early postnatal development. SE may result in important plastic changes in critical periods of brain maturation leading to long-lasting epileptogenesis, as manifested by electrogaphic epileptiform discharges, behavioral deficits, and in vitro hyperexcitability of hippocampal networks.
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spelling Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological studydevelopmentepilepsyhippocampuspilocarpineratPurpose: Animal models are useful for the study of status epilepticus (SE)-induced epileptogenesis and neurological sequelae, especially during early brain development. Here. we show several permanent abnormalities in animals subjected to multiple SE during early development.Methods: Wistar pup rats (7 to 9 days old) were subjected to three consecutive episodes of SE induced by systemic pilocarpine injections. To study the long-lasting consequences of early-induced SE, chronic electroencephalographic recordings were made from the hippocampus and cortex and several behavioral tests (inhibitory step-down avoidance, rota-rod, open field, elevated plus-maze, and Skinner box) were performed at postnatal days 30 to 90. We also investigated in vitro electrophysiological responses of the CA1 area using extracellular recordings in hippocampal slices. A histological analysis was done using cresyl violet staining 24 hours and several months after SE induction. Apoptotic cell death was evaluated by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL staining) 24 hours after the last SE episode.Results: Electloencephalographic recordings from 30- to 90-day-old rats that had been subjected to multiple SE episodes in early life showed marked changes compared with those from nontreated controls. These included frequent episodes of continuous complex spiking activity and high-voltage ictal discharges, with a small percentage of these rats presenting spontaneous behavioral seizures. These animals also presented evidence of severe cognitive deficit in adulthood. in vitro, a persistent hyperexcitability of the CAI area was detected in experimental animals. Histological analysis of the brains did not reveal any major long-term pathological changes. Nevertheless, an increased number of TUNEL-positive nuclei were present in some animals in both the hippocampus and the thalamus.Conclusions: These data show persistent abnormalities in animals subjected to multiple SE episodes during early postnatal development. SE may result in important plastic changes in critical periods of brain maturation leading to long-lasting epileptogenesis, as manifested by electrogaphic epileptiform discharges, behavioral deficits, and in vitro hyperexcitability of hippocampal networks.Universidade Federal de São Paulo, Escola Paulista Med, Lab Neurol Expt, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Lab Neurol Expt, BR-04023900 São Paulo, BrazilWeb of ScienceLippincott Williams & WilkinsUniversidade Federal de São Paulo (UNIFESP)Santos, N. F.Marques, R. H.Correia, L.Sinigaglia-Coimbra, Rita [UNIFESP]Calderazzo, Lineu [UNIFESP]Sanabria, ERGCavalheiro, Esper Abrão [UNIFESP]2016-01-24T12:30:58Z2016-01-24T12:30:58Z2000-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionS57-S63http://dx.doi.org/10.1111/j.1528-1157.2000.tb01558.xEpilepsia. Philadelphia: Lippincott Williams & Wilkins, v. 41, p. S57-S63, 2000.10.1111/j.1528-1157.2000.tb01558.x0013-9580http://repositorio.unifesp.br/handle/11600/26206WOS:000089156500012engEpilepsiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-07-08T10:33:28Zoai:repositorio.unifesp.br/:11600/26206Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-07-08T10:33:28Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
title Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
spellingShingle Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
Santos, N. F.
development
epilepsy
hippocampus
pilocarpine
rat
title_short Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
title_full Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
title_fullStr Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
title_full_unstemmed Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
title_sort Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
author Santos, N. F.
author_facet Santos, N. F.
Marques, R. H.
Correia, L.
Sinigaglia-Coimbra, Rita [UNIFESP]
Calderazzo, Lineu [UNIFESP]
Sanabria, ERG
Cavalheiro, Esper Abrão [UNIFESP]
author_role author
author2 Marques, R. H.
Correia, L.
Sinigaglia-Coimbra, Rita [UNIFESP]
Calderazzo, Lineu [UNIFESP]
Sanabria, ERG
Cavalheiro, Esper Abrão [UNIFESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Santos, N. F.
Marques, R. H.
Correia, L.
Sinigaglia-Coimbra, Rita [UNIFESP]
Calderazzo, Lineu [UNIFESP]
Sanabria, ERG
Cavalheiro, Esper Abrão [UNIFESP]
dc.subject.por.fl_str_mv development
epilepsy
hippocampus
pilocarpine
rat
topic development
epilepsy
hippocampus
pilocarpine
rat
description Purpose: Animal models are useful for the study of status epilepticus (SE)-induced epileptogenesis and neurological sequelae, especially during early brain development. Here. we show several permanent abnormalities in animals subjected to multiple SE during early development.Methods: Wistar pup rats (7 to 9 days old) were subjected to three consecutive episodes of SE induced by systemic pilocarpine injections. To study the long-lasting consequences of early-induced SE, chronic electroencephalographic recordings were made from the hippocampus and cortex and several behavioral tests (inhibitory step-down avoidance, rota-rod, open field, elevated plus-maze, and Skinner box) were performed at postnatal days 30 to 90. We also investigated in vitro electrophysiological responses of the CA1 area using extracellular recordings in hippocampal slices. A histological analysis was done using cresyl violet staining 24 hours and several months after SE induction. Apoptotic cell death was evaluated by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL staining) 24 hours after the last SE episode.Results: Electloencephalographic recordings from 30- to 90-day-old rats that had been subjected to multiple SE episodes in early life showed marked changes compared with those from nontreated controls. These included frequent episodes of continuous complex spiking activity and high-voltage ictal discharges, with a small percentage of these rats presenting spontaneous behavioral seizures. These animals also presented evidence of severe cognitive deficit in adulthood. in vitro, a persistent hyperexcitability of the CAI area was detected in experimental animals. Histological analysis of the brains did not reveal any major long-term pathological changes. Nevertheless, an increased number of TUNEL-positive nuclei were present in some animals in both the hippocampus and the thalamus.Conclusions: These data show persistent abnormalities in animals subjected to multiple SE episodes during early postnatal development. SE may result in important plastic changes in critical periods of brain maturation leading to long-lasting epileptogenesis, as manifested by electrogaphic epileptiform discharges, behavioral deficits, and in vitro hyperexcitability of hippocampal networks.
publishDate 2000
dc.date.none.fl_str_mv 2000-01-01
2016-01-24T12:30:58Z
2016-01-24T12:30:58Z
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.1528-1157.2000.tb01558.x
Epilepsia. Philadelphia: Lippincott Williams & Wilkins, v. 41, p. S57-S63, 2000.
10.1111/j.1528-1157.2000.tb01558.x
0013-9580
http://repositorio.unifesp.br/handle/11600/26206
WOS:000089156500012
url http://dx.doi.org/10.1111/j.1528-1157.2000.tb01558.x
http://repositorio.unifesp.br/handle/11600/26206
identifier_str_mv Epilepsia. Philadelphia: Lippincott Williams & Wilkins, v. 41, p. S57-S63, 2000.
10.1111/j.1528-1157.2000.tb01558.x
0013-9580
WOS:000089156500012
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
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv S57-S63
dc.publisher.none.fl_str_mv Lippincott Williams & Wilkins
publisher.none.fl_str_mv Lippincott Williams & Wilkins
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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