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Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease

Alzheimer’s disease (AD) is a prevalent neurological disorder affecting memory function in elderly persons. Indeed, AD exhibits abnormality in cognitive behaviors and higher susceptibility to neuropsychiatric symptoms (NPS). Various factors including aging, sex difference and NPS severity, are impli...

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Autores principales: Murayama, Masanori A., Arimitsu, Nagisa, Shimizu, Jun, Fujiwara, Naruyoshi, Takai, Kenji, Ikeda, Yoshiki, Okada, Yoko, Hirotsu, Chieko, Takada, Erika, Suzuki, Tomoko, Suzuki, Noboru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Association for Laboratory Animal Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390308/
https://www.ncbi.nlm.nih.gov/pubmed/33840703
http://dx.doi.org/10.1538/expanim.21-0009
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author Murayama, Masanori A.
Arimitsu, Nagisa
Shimizu, Jun
Fujiwara, Naruyoshi
Takai, Kenji
Ikeda, Yoshiki
Okada, Yoko
Hirotsu, Chieko
Takada, Erika
Suzuki, Tomoko
Suzuki, Noboru
author_facet Murayama, Masanori A.
Arimitsu, Nagisa
Shimizu, Jun
Fujiwara, Naruyoshi
Takai, Kenji
Ikeda, Yoshiki
Okada, Yoko
Hirotsu, Chieko
Takada, Erika
Suzuki, Tomoko
Suzuki, Noboru
author_sort Murayama, Masanori A.
collection PubMed
description Alzheimer’s disease (AD) is a prevalent neurological disorder affecting memory function in elderly persons. Indeed, AD exhibits abnormality in cognitive behaviors and higher susceptibility to neuropsychiatric symptoms (NPS). Various factors including aging, sex difference and NPS severity, are implicated during in development of AD. In this study, we evaluated behavioral abnormalities of AD model, PDAPP transgenic mice at young age using the Morris Water Maze test, which was established to assess hippocampal-dependent learning and memory. We found that female AD model mice exhibited spatial learning dysfunction and highly susceptible to NPS such as anxiety and depression, whereas spatial reference memory function was comparable in female PDAPP Tg mice to female wild type (WT) mice. Spatial learning function was comparable in male AD model mice to male WT mice. Multiple regression analysis showed that spatial learning dysfunction was associated with NPS severity such as anxiety and depression. Furthermore, the analysis showed that spatial reference memory function was associated with status of depression, but not anxiety. Thus, these results suggest female dominance of spatial learning dysfunction in the AD model mice accompanying increased NPS severity. The understandings of AD model may be useful for the development of therapeutic agents and methods in human AD.
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spelling pubmed-83903082021-08-31 Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease Murayama, Masanori A. Arimitsu, Nagisa Shimizu, Jun Fujiwara, Naruyoshi Takai, Kenji Ikeda, Yoshiki Okada, Yoko Hirotsu, Chieko Takada, Erika Suzuki, Tomoko Suzuki, Noboru Exp Anim Original Alzheimer’s disease (AD) is a prevalent neurological disorder affecting memory function in elderly persons. Indeed, AD exhibits abnormality in cognitive behaviors and higher susceptibility to neuropsychiatric symptoms (NPS). Various factors including aging, sex difference and NPS severity, are implicated during in development of AD. In this study, we evaluated behavioral abnormalities of AD model, PDAPP transgenic mice at young age using the Morris Water Maze test, which was established to assess hippocampal-dependent learning and memory. We found that female AD model mice exhibited spatial learning dysfunction and highly susceptible to NPS such as anxiety and depression, whereas spatial reference memory function was comparable in female PDAPP Tg mice to female wild type (WT) mice. Spatial learning function was comparable in male AD model mice to male WT mice. Multiple regression analysis showed that spatial learning dysfunction was associated with NPS severity such as anxiety and depression. Furthermore, the analysis showed that spatial reference memory function was associated with status of depression, but not anxiety. Thus, these results suggest female dominance of spatial learning dysfunction in the AD model mice accompanying increased NPS severity. The understandings of AD model may be useful for the development of therapeutic agents and methods in human AD. Japanese Association for Laboratory Animal Science 2021-04-09 2021 /pmc/articles/PMC8390308/ /pubmed/33840703 http://dx.doi.org/10.1538/expanim.21-0009 Text en ©2021 Japanese Association for Laboratory Animal Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original
Murayama, Masanori A.
Arimitsu, Nagisa
Shimizu, Jun
Fujiwara, Naruyoshi
Takai, Kenji
Ikeda, Yoshiki
Okada, Yoko
Hirotsu, Chieko
Takada, Erika
Suzuki, Tomoko
Suzuki, Noboru
Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease
title Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease
title_full Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease
title_fullStr Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease
title_full_unstemmed Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease
title_short Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease
title_sort female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of alzheimer’s disease
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390308/
https://www.ncbi.nlm.nih.gov/pubmed/33840703
http://dx.doi.org/10.1538/expanim.21-0009
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