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Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests

Object recognition tasks detect cognitive deficits in transgenic Alzheimer’s disease (AD) mouse models. Object recognition, however, is not a unitary process, and there are many uncharacterized facets of object processing with relevance to AD. We therefore systematically evaluated object processing...

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Autores principales: Creighton, Samantha D., Mendell, Ari L., Palmer, Daniel, Kalisch, Bettina E., MacLusky, Neil J., Prado, Vania F., Prado, Marco A. M., Winters, Boyer D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329782/
https://www.ncbi.nlm.nih.gov/pubmed/30635592
http://dx.doi.org/10.1038/s41598-018-37312-0
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author Creighton, Samantha D.
Mendell, Ari L.
Palmer, Daniel
Kalisch, Bettina E.
MacLusky, Neil J.
Prado, Vania F.
Prado, Marco A. M.
Winters, Boyer D.
author_facet Creighton, Samantha D.
Mendell, Ari L.
Palmer, Daniel
Kalisch, Bettina E.
MacLusky, Neil J.
Prado, Vania F.
Prado, Marco A. M.
Winters, Boyer D.
author_sort Creighton, Samantha D.
collection PubMed
description Object recognition tasks detect cognitive deficits in transgenic Alzheimer’s disease (AD) mouse models. Object recognition, however, is not a unitary process, and there are many uncharacterized facets of object processing with relevance to AD. We therefore systematically evaluated object processing in 5xFAD and 3xTG AD mice to clarify the nature of object recognition-related deficits. Twelve-month-old male and female 5xFAD and 3xTG mice were assessed on tasks for object identity recognition, spatial recognition, and multisensory object perception. Memory and multisensory perceptual impairments were observed, with interesting dissociations between transgenic AD strains and sex that paralleled neuropathological changes. Overreliance on the widespread “object recognition” task threatens to slow discovery of potentially significant and clinically relevant behavioural effects related to this multifaceted cognitive function. The current results support the use of carefully designed object-based test batteries to clarify the relationship between “object recognition” impairments and specific aspects of AD pathology in rodent models.
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spelling pubmed-63297822019-01-14 Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests Creighton, Samantha D. Mendell, Ari L. Palmer, Daniel Kalisch, Bettina E. MacLusky, Neil J. Prado, Vania F. Prado, Marco A. M. Winters, Boyer D. Sci Rep Article Object recognition tasks detect cognitive deficits in transgenic Alzheimer’s disease (AD) mouse models. Object recognition, however, is not a unitary process, and there are many uncharacterized facets of object processing with relevance to AD. We therefore systematically evaluated object processing in 5xFAD and 3xTG AD mice to clarify the nature of object recognition-related deficits. Twelve-month-old male and female 5xFAD and 3xTG mice were assessed on tasks for object identity recognition, spatial recognition, and multisensory object perception. Memory and multisensory perceptual impairments were observed, with interesting dissociations between transgenic AD strains and sex that paralleled neuropathological changes. Overreliance on the widespread “object recognition” task threatens to slow discovery of potentially significant and clinically relevant behavioural effects related to this multifaceted cognitive function. The current results support the use of carefully designed object-based test batteries to clarify the relationship between “object recognition” impairments and specific aspects of AD pathology in rodent models. Nature Publishing Group UK 2019-01-11 /pmc/articles/PMC6329782/ /pubmed/30635592 http://dx.doi.org/10.1038/s41598-018-37312-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Creighton, Samantha D.
Mendell, Ari L.
Palmer, Daniel
Kalisch, Bettina E.
MacLusky, Neil J.
Prado, Vania F.
Prado, Marco A. M.
Winters, Boyer D.
Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests
title Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests
title_full Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests
title_fullStr Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests
title_full_unstemmed Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests
title_short Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests
title_sort dissociable cognitive impairments in two strains of transgenic alzheimer’s disease mice revealed by a battery of object-based tests
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329782/
https://www.ncbi.nlm.nih.gov/pubmed/30635592
http://dx.doi.org/10.1038/s41598-018-37312-0
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