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Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan

Due to strain-specific behavioral idiosyncrasies, inbred mouse strains are suboptimal research models for behavioral aging studies. The aim of this study is to determine age-related behavioral changes of F2 hybrid C57BL/6NxBALB/c male and female mice. Lifespan was followed (n(males)=48, n(females)=5...

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Autores principales: Adelöf, Julia, Ross, Jaime M., Lazic, Stanley E., Zetterberg, Madeleine, Wiseman, John, Hernebring, Malin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756906/
https://www.ncbi.nlm.nih.gov/pubmed/31509518
http://dx.doi.org/10.18632/aging.102242
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author Adelöf, Julia
Ross, Jaime M.
Lazic, Stanley E.
Zetterberg, Madeleine
Wiseman, John
Hernebring, Malin
author_facet Adelöf, Julia
Ross, Jaime M.
Lazic, Stanley E.
Zetterberg, Madeleine
Wiseman, John
Hernebring, Malin
author_sort Adelöf, Julia
collection PubMed
description Due to strain-specific behavioral idiosyncrasies, inbred mouse strains are suboptimal research models for behavioral aging studies. The aim of this study is to determine age-related behavioral changes of F2 hybrid C57BL/6NxBALB/c male and female mice. Lifespan was followed (n(males)=48, n(females)=51) and cohorts of mature adult (7 months), middle-aged (15 months), and old mice (22 months of age; n=7-12 per group) were assessed regarding open-field activity, exploration, passive avoidance learning/memory, and depressive-like behavior. We found that both males and females demonstrated decreased exploratory behavior with age, while memory and depressive-like behavior were maintained. Females exhibited enhanced depressive-like behavior compared to males; however, a correlation between fat mass and swimming activity in the test directly accounted for 30-46% of this behavioral sex difference. In addition, we suggest a method to qualitatively estimate natural lifespan from survival analyses in which animals with signs of pain or severe disease are euthanized. This is, to our knowledge, the first behavioral study to consider both sex and aging in hybrid mice. We here define decreased exploratory behavior as a conserved hallmark of aging independent of sex, highlight the effect of buoyancy in water tests, and provide a method to assay lifespan with reduced animal suffering.
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spelling pubmed-67569062019-09-27 Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan Adelöf, Julia Ross, Jaime M. Lazic, Stanley E. Zetterberg, Madeleine Wiseman, John Hernebring, Malin Aging (Albany NY) Research Paper Due to strain-specific behavioral idiosyncrasies, inbred mouse strains are suboptimal research models for behavioral aging studies. The aim of this study is to determine age-related behavioral changes of F2 hybrid C57BL/6NxBALB/c male and female mice. Lifespan was followed (n(males)=48, n(females)=51) and cohorts of mature adult (7 months), middle-aged (15 months), and old mice (22 months of age; n=7-12 per group) were assessed regarding open-field activity, exploration, passive avoidance learning/memory, and depressive-like behavior. We found that both males and females demonstrated decreased exploratory behavior with age, while memory and depressive-like behavior were maintained. Females exhibited enhanced depressive-like behavior compared to males; however, a correlation between fat mass and swimming activity in the test directly accounted for 30-46% of this behavioral sex difference. In addition, we suggest a method to qualitatively estimate natural lifespan from survival analyses in which animals with signs of pain or severe disease are euthanized. This is, to our knowledge, the first behavioral study to consider both sex and aging in hybrid mice. We here define decreased exploratory behavior as a conserved hallmark of aging independent of sex, highlight the effect of buoyancy in water tests, and provide a method to assay lifespan with reduced animal suffering. Impact Journals 2019-09-11 /pmc/articles/PMC6756906/ /pubmed/31509518 http://dx.doi.org/10.18632/aging.102242 Text en Copyright © 2019 Adelöf et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Adelöf, Julia
Ross, Jaime M.
Lazic, Stanley E.
Zetterberg, Madeleine
Wiseman, John
Hernebring, Malin
Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan
title Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan
title_full Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan
title_fullStr Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan
title_full_unstemmed Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan
title_short Conclusions from a behavioral aging study on male and female F2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan
title_sort conclusions from a behavioral aging study on male and female f2 hybrid mice on age-related behavior, buoyancy in water-based tests, and an ethical method to assess lifespan
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756906/
https://www.ncbi.nlm.nih.gov/pubmed/31509518
http://dx.doi.org/10.18632/aging.102242
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