Multiple pilocarpine-induced status epilepticus in developing rats: A long-term behavioral and electrophysiological study
Autor(a) principal: | |
---|---|
Data de Publicação: | 2000 |
Outros Autores: | , , , , , |
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. |
id |
UFSP_94294317b9a88e3f2f418cf1d1695e29 |
---|---|
oai_identifier_str |
oai:repositorio.unifesp.br/:11600/26206 |
network_acronym_str |
UFSP |
network_name_str |
Repositório Institucional da UNIFESP |
repository_id_str |
3465 |
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 |
_version_ |
1814268294153109504 |