Cargando…

Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats

Increased adult neurogenesis is observed after training in hippocampal-dependent tasks and also after acutely induced status epilepticus (SE) although the specific roles of these cells are still a matter of debate. In this study, we investigated hippocampal cell proliferation and differentiation and...

Descripción completa

Detalles Bibliográficos
Autores principales: Cavarsan, Clarissa F., Queiroz, Claudio M., dos Santos, Jair Guilherme, Xavier, Gilberto F., Mello, Luiz Eugênio, Covolan, Luciene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724058/
https://www.ncbi.nlm.nih.gov/pubmed/23898322
http://dx.doi.org/10.3389/fneur.2013.00106
_version_ 1782476637581869056
author Cavarsan, Clarissa F.
Queiroz, Claudio M.
dos Santos, Jair Guilherme
Xavier, Gilberto F.
Mello, Luiz Eugênio
Covolan, Luciene
author_facet Cavarsan, Clarissa F.
Queiroz, Claudio M.
dos Santos, Jair Guilherme
Xavier, Gilberto F.
Mello, Luiz Eugênio
Covolan, Luciene
author_sort Cavarsan, Clarissa F.
collection PubMed
description Increased adult neurogenesis is observed after training in hippocampal-dependent tasks and also after acutely induced status epilepticus (SE) although the specific roles of these cells are still a matter of debate. In this study, we investigated hippocampal cell proliferation and differentiation and the spatial learning performance in young or aged chronically epileptic rats. Status was induced by pilocarpine in 3 or 20-month old rats. Either 2 or 20 months later, rats were treated with bromodeoxyuridine (BrdU) and subsequently underwent to 8-day schedule of water maze (WM) tests. As expected, learning curves were faster in young than in aged animals (P < 0.001). Chronically epileptic animals exhibited impaired learning curves compared to age-matched controls. Interestingly, the duration of epilepsy (2 or 20 months) did not correlate with the memory impairment of aged-epileptic animals. The number of BrdU-positive cells was greater in young-epileptic subjects than in age-matched controls. In contrast, cell proliferation was not increased in aged-epileptic animals, irrespective of the time of SE induction. Finally, dentate cell proliferation was not related to performance in the WM. Based on the present results we conclude that even though aging and epilepsy lead to impairments in spatial learning, their effects are not additive.
format Online
Article
Text
id pubmed-3724058
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-37240582013-07-29 Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats Cavarsan, Clarissa F. Queiroz, Claudio M. dos Santos, Jair Guilherme Xavier, Gilberto F. Mello, Luiz Eugênio Covolan, Luciene Front Neurol Neuroscience Increased adult neurogenesis is observed after training in hippocampal-dependent tasks and also after acutely induced status epilepticus (SE) although the specific roles of these cells are still a matter of debate. In this study, we investigated hippocampal cell proliferation and differentiation and the spatial learning performance in young or aged chronically epileptic rats. Status was induced by pilocarpine in 3 or 20-month old rats. Either 2 or 20 months later, rats were treated with bromodeoxyuridine (BrdU) and subsequently underwent to 8-day schedule of water maze (WM) tests. As expected, learning curves were faster in young than in aged animals (P < 0.001). Chronically epileptic animals exhibited impaired learning curves compared to age-matched controls. Interestingly, the duration of epilepsy (2 or 20 months) did not correlate with the memory impairment of aged-epileptic animals. The number of BrdU-positive cells was greater in young-epileptic subjects than in age-matched controls. In contrast, cell proliferation was not increased in aged-epileptic animals, irrespective of the time of SE induction. Finally, dentate cell proliferation was not related to performance in the WM. Based on the present results we conclude that even though aging and epilepsy lead to impairments in spatial learning, their effects are not additive. Frontiers Media S.A. 2013-07-26 /pmc/articles/PMC3724058/ /pubmed/23898322 http://dx.doi.org/10.3389/fneur.2013.00106 Text en Copyright© 2013 Cavarsan, Queiroz, dos Santos, Xavier, Mello and Covolan. 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
Cavarsan, Clarissa F.
Queiroz, Claudio M.
dos Santos, Jair Guilherme
Xavier, Gilberto F.
Mello, Luiz Eugênio
Covolan, Luciene
Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats
title Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats
title_full Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats
title_fullStr Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats
title_full_unstemmed Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats
title_short Reduced Hippocampal Dentate Cell Proliferation and Impaired Spatial Memory Performance in Aged-Epileptic Rats
title_sort reduced hippocampal dentate cell proliferation and impaired spatial memory performance in aged-epileptic rats
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724058/
https://www.ncbi.nlm.nih.gov/pubmed/23898322
http://dx.doi.org/10.3389/fneur.2013.00106
work_keys_str_mv AT cavarsanclarissaf reducedhippocampaldentatecellproliferationandimpairedspatialmemoryperformanceinagedepilepticrats
AT queirozclaudiom reducedhippocampaldentatecellproliferationandimpairedspatialmemoryperformanceinagedepilepticrats
AT dossantosjairguilherme reducedhippocampaldentatecellproliferationandimpairedspatialmemoryperformanceinagedepilepticrats
AT xaviergilbertof reducedhippocampaldentatecellproliferationandimpairedspatialmemoryperformanceinagedepilepticrats
AT melloluizeugenio reducedhippocampaldentatecellproliferationandimpairedspatialmemoryperformanceinagedepilepticrats
AT covolanluciene reducedhippocampaldentatecellproliferationandimpairedspatialmemoryperformanceinagedepilepticrats