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Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging

Alzheimer’s disease (AD) is characterized by brain plaques, tangles, and cognitive impairment. AD is one of the most common age-related dementias in humans. Progress in characterizing AD and other age-related disorders is hindered by a perceived dearth of animal models that naturally reproduce disea...

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Autores principales: de Sousa, Alexandra A., Rigby Dames, Brier A., Graff, Emily C., Mohamedelhassan, Rania, Vassilopoulos, Tatianna, Charvet, Christine J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284893/
https://www.ncbi.nlm.nih.gov/pubmed/37344566
http://dx.doi.org/10.1038/s42003-023-05034-3
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author de Sousa, Alexandra A.
Rigby Dames, Brier A.
Graff, Emily C.
Mohamedelhassan, Rania
Vassilopoulos, Tatianna
Charvet, Christine J.
author_facet de Sousa, Alexandra A.
Rigby Dames, Brier A.
Graff, Emily C.
Mohamedelhassan, Rania
Vassilopoulos, Tatianna
Charvet, Christine J.
author_sort de Sousa, Alexandra A.
collection PubMed
description Alzheimer’s disease (AD) is characterized by brain plaques, tangles, and cognitive impairment. AD is one of the most common age-related dementias in humans. Progress in characterizing AD and other age-related disorders is hindered by a perceived dearth of animal models that naturally reproduce diseases observed in humans. Mice and nonhuman primates are model systems used to understand human diseases. Still, these model systems lack many of the biological characteristics of Alzheimer-like diseases (e.g., plaques, tangles) as they grow older. In contrast, companion animal models (cats and dogs) age in ways that resemble humans. Both companion animal models and humans show evidence of brain atrophy, plaques, and tangles, as well as cognitive decline with age. We embrace a One Health perspective, which recognizes that the health of humans is connected to those of animals, and we illustrate how such a perspective can work synergistically to enhance human and animal health. A comparative biology perspective is ideally suited to integrate insights across veterinary and human medical disciplines and solve long-standing problems in aging.
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spelling pubmed-102848932023-06-23 Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging de Sousa, Alexandra A. Rigby Dames, Brier A. Graff, Emily C. Mohamedelhassan, Rania Vassilopoulos, Tatianna Charvet, Christine J. Commun Biol Perspective Alzheimer’s disease (AD) is characterized by brain plaques, tangles, and cognitive impairment. AD is one of the most common age-related dementias in humans. Progress in characterizing AD and other age-related disorders is hindered by a perceived dearth of animal models that naturally reproduce diseases observed in humans. Mice and nonhuman primates are model systems used to understand human diseases. Still, these model systems lack many of the biological characteristics of Alzheimer-like diseases (e.g., plaques, tangles) as they grow older. In contrast, companion animal models (cats and dogs) age in ways that resemble humans. Both companion animal models and humans show evidence of brain atrophy, plaques, and tangles, as well as cognitive decline with age. We embrace a One Health perspective, which recognizes that the health of humans is connected to those of animals, and we illustrate how such a perspective can work synergistically to enhance human and animal health. A comparative biology perspective is ideally suited to integrate insights across veterinary and human medical disciplines and solve long-standing problems in aging. Nature Publishing Group UK 2023-06-21 /pmc/articles/PMC10284893/ /pubmed/37344566 http://dx.doi.org/10.1038/s42003-023-05034-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Perspective
de Sousa, Alexandra A.
Rigby Dames, Brier A.
Graff, Emily C.
Mohamedelhassan, Rania
Vassilopoulos, Tatianna
Charvet, Christine J.
Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging
title Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging
title_full Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging
title_fullStr Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging
title_full_unstemmed Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging
title_short Going beyond established model systems of Alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging
title_sort going beyond established model systems of alzheimer’s disease: companion animals provide novel insights into the neurobiology of aging
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284893/
https://www.ncbi.nlm.nih.gov/pubmed/37344566
http://dx.doi.org/10.1038/s42003-023-05034-3
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