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Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats

Using animal models to study the underlying mechanisms of aging will create a critical foundation from which to develop new interventions for aging-related brain disorders. Aging-related reorganization of the brain network has been described for the human brain based on functional, metabolic and str...

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Autores principales: Xue, Xin, Wu, Jia-Jia, Huo, Bei-Bei, Xing, Xiang-Xin, Ma, Jie, Li, Yu-Lin, Zheng, Mou-Xiong, Hua, Xu-Yun, Xu, Jian-Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833125/
https://www.ncbi.nlm.nih.gov/pubmed/35077393
http://dx.doi.org/10.18632/aging.203851
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author Xue, Xin
Wu, Jia-Jia
Huo, Bei-Bei
Xing, Xiang-Xin
Ma, Jie
Li, Yu-Lin
Zheng, Mou-Xiong
Hua, Xu-Yun
Xu, Jian-Guang
author_facet Xue, Xin
Wu, Jia-Jia
Huo, Bei-Bei
Xing, Xiang-Xin
Ma, Jie
Li, Yu-Lin
Zheng, Mou-Xiong
Hua, Xu-Yun
Xu, Jian-Guang
author_sort Xue, Xin
collection PubMed
description Using animal models to study the underlying mechanisms of aging will create a critical foundation from which to develop new interventions for aging-related brain disorders. Aging-related reorganization of the brain network has been described for the human brain based on functional, metabolic and structural connectivity. However, alterations in the brain metabolic network of aging rats remain unknown. Here, we submitted young and aged rats to [18F]fluorodeoxyglucose with positron emission tomography (18F-FDG PET) and constructed brain metabolic networks. The topological properties were detected, and the network robustness against random failures and targeted attacks was analyzed for age-group comparison. Compared with young rats, aged rats showed reduced betweenness centrality (BC) in the superior colliculus and a decreased degree (D) in the parietal association cortex. With regard to network robustness, the brain metabolic networks of aged rats were more vulnerable to simulated damage, which showed significantly lower local efficiency and clustering coefficients than those of the young rats against targeted attacks and random failures. The findings support the idea that aged rats have similar aging-related changes in the brain metabolic network to the human brain and can therefore be used as a model for aging studies to provide targets for potential therapies that promote healthy aging.
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spelling pubmed-88331252022-02-14 Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats Xue, Xin Wu, Jia-Jia Huo, Bei-Bei Xing, Xiang-Xin Ma, Jie Li, Yu-Lin Zheng, Mou-Xiong Hua, Xu-Yun Xu, Jian-Guang Aging (Albany NY) Research Paper Using animal models to study the underlying mechanisms of aging will create a critical foundation from which to develop new interventions for aging-related brain disorders. Aging-related reorganization of the brain network has been described for the human brain based on functional, metabolic and structural connectivity. However, alterations in the brain metabolic network of aging rats remain unknown. Here, we submitted young and aged rats to [18F]fluorodeoxyglucose with positron emission tomography (18F-FDG PET) and constructed brain metabolic networks. The topological properties were detected, and the network robustness against random failures and targeted attacks was analyzed for age-group comparison. Compared with young rats, aged rats showed reduced betweenness centrality (BC) in the superior colliculus and a decreased degree (D) in the parietal association cortex. With regard to network robustness, the brain metabolic networks of aged rats were more vulnerable to simulated damage, which showed significantly lower local efficiency and clustering coefficients than those of the young rats against targeted attacks and random failures. The findings support the idea that aged rats have similar aging-related changes in the brain metabolic network to the human brain and can therefore be used as a model for aging studies to provide targets for potential therapies that promote healthy aging. Impact Journals 2022-01-25 /pmc/articles/PMC8833125/ /pubmed/35077393 http://dx.doi.org/10.18632/aging.203851 Text en Copyright: © 2022 Xue et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (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
Xue, Xin
Wu, Jia-Jia
Huo, Bei-Bei
Xing, Xiang-Xin
Ma, Jie
Li, Yu-Lin
Zheng, Mou-Xiong
Hua, Xu-Yun
Xu, Jian-Guang
Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats
title Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats
title_full Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats
title_fullStr Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats
title_full_unstemmed Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats
title_short Age-related alterations of brain metabolic network based on [18F]FDG-PET of rats
title_sort age-related alterations of brain metabolic network based on [18f]fdg-pet of rats
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833125/
https://www.ncbi.nlm.nih.gov/pubmed/35077393
http://dx.doi.org/10.18632/aging.203851
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