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Characterization of aged male BALB/c(cenp) mice as a model of dementia

Dementia is defined as cognitive impairment in more than one cognitive area and leads to an abnormal degree of impairment in the ability to remember past events. Among mice models of dementia the most used strains are SAMP8 and C57BL/6. There is no reference to characterizing a model of dementia in...

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Autores principales: Esquivel, Nashelly, García, Yenela, Lores, Bestraida, Gutiérrez, Marivy, Rodríguez, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081599/
https://www.ncbi.nlm.nih.gov/pubmed/32206613
http://dx.doi.org/10.1186/s42826-020-00038-0
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author Esquivel, Nashelly
García, Yenela
Lores, Bestraida
Gutiérrez, Marivy
Rodríguez, Claudio
author_facet Esquivel, Nashelly
García, Yenela
Lores, Bestraida
Gutiérrez, Marivy
Rodríguez, Claudio
author_sort Esquivel, Nashelly
collection PubMed
description Dementia is defined as cognitive impairment in more than one cognitive area and leads to an abnormal degree of impairment in the ability to remember past events. Among mice models of dementia the most used strains are SAMP8 and C57BL/6. There is no reference to characterizing a model of dementia in naturally aged mice of the BALB/c strain, or to the minimum age at which these animals can be used. The aim of this study was the characterization of aged male BALB/c(cenp) mice as a model of dementia from the evaluation of behavioural, pathological and biochemical markers. One hundred and twenty mice were used and 10 of these were analysed from 8 to 9 months of age, and every 4 months, in a comparative way to young control animals from 4 to 5 months. At the age of 12–13 months there was cognitive impairment in the animals from the Y-maze and object recognition tests and this impairment was maintained at 16–17 months of age. An increase in oxidative damage to proteins in the brains of aged animals was also found in relation to young animals; as well as a decrease in the concentration of triglycerides. At the age of 16–17 months, a significant decrease in the size of the thymus and brain was obtained. We consider that it’s a very useful option to use animals 12–13 months of age where there are symptoms of cognitive deficiency, histopathological and biochemical elements characteristic of dementia.
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spelling pubmed-70815992020-03-23 Characterization of aged male BALB/c(cenp) mice as a model of dementia Esquivel, Nashelly García, Yenela Lores, Bestraida Gutiérrez, Marivy Rodríguez, Claudio Lab Anim Res Research Dementia is defined as cognitive impairment in more than one cognitive area and leads to an abnormal degree of impairment in the ability to remember past events. Among mice models of dementia the most used strains are SAMP8 and C57BL/6. There is no reference to characterizing a model of dementia in naturally aged mice of the BALB/c strain, or to the minimum age at which these animals can be used. The aim of this study was the characterization of aged male BALB/c(cenp) mice as a model of dementia from the evaluation of behavioural, pathological and biochemical markers. One hundred and twenty mice were used and 10 of these were analysed from 8 to 9 months of age, and every 4 months, in a comparative way to young control animals from 4 to 5 months. At the age of 12–13 months there was cognitive impairment in the animals from the Y-maze and object recognition tests and this impairment was maintained at 16–17 months of age. An increase in oxidative damage to proteins in the brains of aged animals was also found in relation to young animals; as well as a decrease in the concentration of triglycerides. At the age of 16–17 months, a significant decrease in the size of the thymus and brain was obtained. We consider that it’s a very useful option to use animals 12–13 months of age where there are symptoms of cognitive deficiency, histopathological and biochemical elements characteristic of dementia. BioMed Central 2020-03-05 /pmc/articles/PMC7081599/ /pubmed/32206613 http://dx.doi.org/10.1186/s42826-020-00038-0 Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Esquivel, Nashelly
García, Yenela
Lores, Bestraida
Gutiérrez, Marivy
Rodríguez, Claudio
Characterization of aged male BALB/c(cenp) mice as a model of dementia
title Characterization of aged male BALB/c(cenp) mice as a model of dementia
title_full Characterization of aged male BALB/c(cenp) mice as a model of dementia
title_fullStr Characterization of aged male BALB/c(cenp) mice as a model of dementia
title_full_unstemmed Characterization of aged male BALB/c(cenp) mice as a model of dementia
title_short Characterization of aged male BALB/c(cenp) mice as a model of dementia
title_sort characterization of aged male balb/c(cenp) mice as a model of dementia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081599/
https://www.ncbi.nlm.nih.gov/pubmed/32206613
http://dx.doi.org/10.1186/s42826-020-00038-0
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