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Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures

Neonatal seizures are the most common manifestation of neurological dysfunction in the neonate. The prognosis of neonatal seizures is highly variable, and the controversy remains whether the severity, duration, or frequency of seizures may contribute to brain damage independently of its etiology. An...

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Autores principales: Castelhano, Adelisandra Silva Santos, Cassane, Gustavo dos Santos Teada, Scorza, Fulvio Alexandre, Cysneiros, Roberta Monterazzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648772/
https://www.ncbi.nlm.nih.gov/pubmed/23675329
http://dx.doi.org/10.3389/fnbeh.2013.00036
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author Castelhano, Adelisandra Silva Santos
Cassane, Gustavo dos Santos Teada
Scorza, Fulvio Alexandre
Cysneiros, Roberta Monterazzo
author_facet Castelhano, Adelisandra Silva Santos
Cassane, Gustavo dos Santos Teada
Scorza, Fulvio Alexandre
Cysneiros, Roberta Monterazzo
author_sort Castelhano, Adelisandra Silva Santos
collection PubMed
description Neonatal seizures are the most common manifestation of neurological dysfunction in the neonate. The prognosis of neonatal seizures is highly variable, and the controversy remains whether the severity, duration, or frequency of seizures may contribute to brain damage independently of its etiology. Animal data indicates that seizures during development are associated with a high probability of long-term adverse effects such as learning and memory impairment, behavioral changes and even epilepsy, which is strongly age dependent, as well as the severity, duration, and frequency of seizures. In preliminary studies, we demonstrated that adolescent male rats exposed to one-single neonatal status epilepticus (SE) episode showed social behavior impairment, and we proposed the model as relevant for studies of developmental disorders. Based on these facts, the goal of this study was to verify the existence of a persistent deficit and if the anxiety-related behavior could be associated with that impairment. To do so, male Wistar rats at 9 days postnatal were submitted to a single episode of SE by pilocarpine injection (380 mg/kg, i.p.) and control animals received saline (0.9%, 0.1 mL/10 g). It was possible to demonstrate that in adulthood, animals exposed to neonatal SE displayed low preference for social novelty, anxiety-related behavior, and increased stereotyped behavior in anxiogenic environment with no locomotor activity changes. On the balance, these data suggests that neonatal SE in rodents leads to altered anxiety-related and abnormal social behaviors.
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spelling pubmed-36487722013-05-14 Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures Castelhano, Adelisandra Silva Santos Cassane, Gustavo dos Santos Teada Scorza, Fulvio Alexandre Cysneiros, Roberta Monterazzo Front Behav Neurosci Neuroscience Neonatal seizures are the most common manifestation of neurological dysfunction in the neonate. The prognosis of neonatal seizures is highly variable, and the controversy remains whether the severity, duration, or frequency of seizures may contribute to brain damage independently of its etiology. Animal data indicates that seizures during development are associated with a high probability of long-term adverse effects such as learning and memory impairment, behavioral changes and even epilepsy, which is strongly age dependent, as well as the severity, duration, and frequency of seizures. In preliminary studies, we demonstrated that adolescent male rats exposed to one-single neonatal status epilepticus (SE) episode showed social behavior impairment, and we proposed the model as relevant for studies of developmental disorders. Based on these facts, the goal of this study was to verify the existence of a persistent deficit and if the anxiety-related behavior could be associated with that impairment. To do so, male Wistar rats at 9 days postnatal were submitted to a single episode of SE by pilocarpine injection (380 mg/kg, i.p.) and control animals received saline (0.9%, 0.1 mL/10 g). It was possible to demonstrate that in adulthood, animals exposed to neonatal SE displayed low preference for social novelty, anxiety-related behavior, and increased stereotyped behavior in anxiogenic environment with no locomotor activity changes. On the balance, these data suggests that neonatal SE in rodents leads to altered anxiety-related and abnormal social behaviors. Frontiers Media S.A. 2013-05-09 /pmc/articles/PMC3648772/ /pubmed/23675329 http://dx.doi.org/10.3389/fnbeh.2013.00036 Text en Copyright © 2013 Castelhano, Cassane, Scorza and Cysneiros. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Castelhano, Adelisandra Silva Santos
Cassane, Gustavo dos Santos Teada
Scorza, Fulvio Alexandre
Cysneiros, Roberta Monterazzo
Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures
title Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures
title_full Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures
title_fullStr Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures
title_full_unstemmed Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures
title_short Altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures
title_sort altered anxiety-related and abnormal social behaviors in rats exposed to early life seizures
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648772/
https://www.ncbi.nlm.nih.gov/pubmed/23675329
http://dx.doi.org/10.3389/fnbeh.2013.00036
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