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Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease

Alzheimer's disease is the most frequent form of dementia in elderly people. The triple transgenic (3xTg‐AD) mouse model of Alzheimer's Disease is important in biomedical research as these mice develop both neuropathological and behavioural phenotypes. However, their behavioural phenotype...

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Autores principales: Simanaviciute, Ugne, Brown, Richard E., Wong, Aimee, Fertan, Emre, Grant, Robyn A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744487/
https://www.ncbi.nlm.nih.gov/pubmed/35733405
http://dx.doi.org/10.1111/gbb.12813
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author Simanaviciute, Ugne
Brown, Richard E.
Wong, Aimee
Fertan, Emre
Grant, Robyn A.
author_facet Simanaviciute, Ugne
Brown, Richard E.
Wong, Aimee
Fertan, Emre
Grant, Robyn A.
author_sort Simanaviciute, Ugne
collection PubMed
description Alzheimer's disease is the most frequent form of dementia in elderly people. The triple transgenic (3xTg‐AD) mouse model of Alzheimer's Disease is important in biomedical research as these mice develop both neuropathological and behavioural phenotypes. However, their behavioural phenotype is variable, with findings depending on the specific task, as well as the age and sex of the mice. Whisker movements show motor, sensory and cognitive deficits in mouse models of neurodegenerative disease. Therefore, we examined whisker movements in 3, 12.5 and 17‐month‐old female 3xTg‐AD mice and their B6129S/F2 wildtype controls. Mice were filmed using a high‐speed video camera (500 fps) in an open arena during a novel object exploration task. Genotype and age differences were found in mice exploring the arena prior to object contact. Prior to whisker contact, the 3‐month‐old 3xTg‐AD mice had smaller whisker angles compared with the wildtype controls, suggesting an early motor phenotype in these mice. Pre‐contact mean angular position at 3 months and whisking amplitude at 17 months of age differed between the 3xTg‐AD and wildtype mice. During object contact 3xTg‐AD mice did not reduce whisker spread as frequently as the wildtype mice at 12.5 and 17 months, which may suggest sensory or attentional deficits. We show that whisker movements are a powerful behavioural measurement tool for capturing behavioural deficits in mouse models that show complex phenotypes, such as the 3xTg‐AD mouse model.
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spelling pubmed-97444872023-02-08 Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease Simanaviciute, Ugne Brown, Richard E. Wong, Aimee Fertan, Emre Grant, Robyn A. Genes Brain Behav Original Articles Alzheimer's disease is the most frequent form of dementia in elderly people. The triple transgenic (3xTg‐AD) mouse model of Alzheimer's Disease is important in biomedical research as these mice develop both neuropathological and behavioural phenotypes. However, their behavioural phenotype is variable, with findings depending on the specific task, as well as the age and sex of the mice. Whisker movements show motor, sensory and cognitive deficits in mouse models of neurodegenerative disease. Therefore, we examined whisker movements in 3, 12.5 and 17‐month‐old female 3xTg‐AD mice and their B6129S/F2 wildtype controls. Mice were filmed using a high‐speed video camera (500 fps) in an open arena during a novel object exploration task. Genotype and age differences were found in mice exploring the arena prior to object contact. Prior to whisker contact, the 3‐month‐old 3xTg‐AD mice had smaller whisker angles compared with the wildtype controls, suggesting an early motor phenotype in these mice. Pre‐contact mean angular position at 3 months and whisking amplitude at 17 months of age differed between the 3xTg‐AD and wildtype mice. During object contact 3xTg‐AD mice did not reduce whisker spread as frequently as the wildtype mice at 12.5 and 17 months, which may suggest sensory or attentional deficits. We show that whisker movements are a powerful behavioural measurement tool for capturing behavioural deficits in mouse models that show complex phenotypes, such as the 3xTg‐AD mouse model. Blackwell Publishing Ltd 2022-06-22 /pmc/articles/PMC9744487/ /pubmed/35733405 http://dx.doi.org/10.1111/gbb.12813 Text en © 2022 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Simanaviciute, Ugne
Brown, Richard E.
Wong, Aimee
Fertan, Emre
Grant, Robyn A.
Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease
title Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease
title_full Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease
title_fullStr Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease
title_full_unstemmed Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease
title_short Abnormal whisker movements in the 3xTg‐AD mouse model of Alzheimer's disease
title_sort abnormal whisker movements in the 3xtg‐ad mouse model of alzheimer's disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744487/
https://www.ncbi.nlm.nih.gov/pubmed/35733405
http://dx.doi.org/10.1111/gbb.12813
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