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Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice

The knockout mouse model, B6.129P2-Apoe(tm1Unc) is homozygotic for the Apolipoprotein E (ApoE) deletion; thus, it is capable of developing hyperlipidemia and atherosclerosis but ApoE is also a lipid-transport protein abundantly expressed in most neurons in the central nervous system, so these animal...

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Autores principales: Fuentes, Dasha, Fernández, Nidia, García, Yenela, García, Teidy, Morales, Ana Ruth, Menéndez, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867486/
https://www.ncbi.nlm.nih.gov/pubmed/29510495
http://dx.doi.org/10.3390/bs8030033
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author Fuentes, Dasha
Fernández, Nidia
García, Yenela
García, Teidy
Morales, Ana Ruth
Menéndez, Roberto
author_facet Fuentes, Dasha
Fernández, Nidia
García, Yenela
García, Teidy
Morales, Ana Ruth
Menéndez, Roberto
author_sort Fuentes, Dasha
collection PubMed
description The knockout mouse model, B6.129P2-Apoe(tm1Unc) is homozygotic for the Apolipoprotein E (ApoE) deletion; thus, it is capable of developing hyperlipidemia and atherosclerosis but ApoE is also a lipid-transport protein abundantly expressed in most neurons in the central nervous system, so these animals could also be models of neurodegenerative diseases. The aim of this study was to determine age-related changes in spontaneous behavior and in learning and memory of Apolipoprotein E knockout mice. Spontaneous behavioral measurements included sleeping pattern, motor coordination and balance by rotarod and open field activity, whereas learning and memory tests included forced alternation in Y-maze, novel object recognition and passive avoidance conditioning. Significant behavioral differences between aged knockout mice and age-matched wild type strain, C57Bl/6 were found in all the behavioral tests, except for the rotarod test. Genetically’ modified mice exhibited less huddling contact during sleeping, decreased locomotor activity in novel environments and in learning and memory deficits. These results are consistent with the cognitive impairment and memory loss seen as the earliest clinical symptoms in neurodegenerative disorders such as Alzheimer’s disease. The ApoE knockout mice might therefore be an appropriate model for studying the underlying mechanisms involved in behavioral changes caused by neurodegenerative diseases as well as for evaluating new therapies for these pathologies.
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spelling pubmed-58674862018-03-27 Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice Fuentes, Dasha Fernández, Nidia García, Yenela García, Teidy Morales, Ana Ruth Menéndez, Roberto Behav Sci (Basel) Article The knockout mouse model, B6.129P2-Apoe(tm1Unc) is homozygotic for the Apolipoprotein E (ApoE) deletion; thus, it is capable of developing hyperlipidemia and atherosclerosis but ApoE is also a lipid-transport protein abundantly expressed in most neurons in the central nervous system, so these animals could also be models of neurodegenerative diseases. The aim of this study was to determine age-related changes in spontaneous behavior and in learning and memory of Apolipoprotein E knockout mice. Spontaneous behavioral measurements included sleeping pattern, motor coordination and balance by rotarod and open field activity, whereas learning and memory tests included forced alternation in Y-maze, novel object recognition and passive avoidance conditioning. Significant behavioral differences between aged knockout mice and age-matched wild type strain, C57Bl/6 were found in all the behavioral tests, except for the rotarod test. Genetically’ modified mice exhibited less huddling contact during sleeping, decreased locomotor activity in novel environments and in learning and memory deficits. These results are consistent with the cognitive impairment and memory loss seen as the earliest clinical symptoms in neurodegenerative disorders such as Alzheimer’s disease. The ApoE knockout mice might therefore be an appropriate model for studying the underlying mechanisms involved in behavioral changes caused by neurodegenerative diseases as well as for evaluating new therapies for these pathologies. MDPI 2018-03-03 /pmc/articles/PMC5867486/ /pubmed/29510495 http://dx.doi.org/10.3390/bs8030033 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fuentes, Dasha
Fernández, Nidia
García, Yenela
García, Teidy
Morales, Ana Ruth
Menéndez, Roberto
Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice
title Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice
title_full Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice
title_fullStr Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice
title_full_unstemmed Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice
title_short Age-Related Changes in the Behavior of Apolipoprotein E Knockout Mice
title_sort age-related changes in the behavior of apolipoprotein e knockout mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867486/
https://www.ncbi.nlm.nih.gov/pubmed/29510495
http://dx.doi.org/10.3390/bs8030033
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