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Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice

Alzheimer’s disease (AD) affects an estimated 5.8 million Americans, and advanced age is the greatest risk factor. AD patients have altered intestinal microbiota. Accordingly, depleting intestinal microbiota in AD animal models reduces amyloid-beta (Aβ) plaque deposition. Age-related changes in the...

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Autores principales: Cox, Laura M., Schafer, Marissa J., Sohn, Jiho, Vincentini, Julia, Weiner, Howard L., Ginsberg, Stephen D., Blaser, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6884494/
https://www.ncbi.nlm.nih.gov/pubmed/31784610
http://dx.doi.org/10.1038/s41598-019-54187-x
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author Cox, Laura M.
Schafer, Marissa J.
Sohn, Jiho
Vincentini, Julia
Weiner, Howard L.
Ginsberg, Stephen D.
Blaser, Martin J.
author_facet Cox, Laura M.
Schafer, Marissa J.
Sohn, Jiho
Vincentini, Julia
Weiner, Howard L.
Ginsberg, Stephen D.
Blaser, Martin J.
author_sort Cox, Laura M.
collection PubMed
description Alzheimer’s disease (AD) affects an estimated 5.8 million Americans, and advanced age is the greatest risk factor. AD patients have altered intestinal microbiota. Accordingly, depleting intestinal microbiota in AD animal models reduces amyloid-beta (Aβ) plaque deposition. Age-related changes in the microbiota contribute to immunologic and physiologic decline. Translationally relevant dietary manipulations may be an effective approach to slow microbiota changes during aging. We previously showed that calorie restriction (CR) reduced brain Aβ deposition in the well-established Tg2576 mouse model of AD. Presently, we investigated whether CR alters the microbiome during aging. We found that female Tg2576 mice have more substantial age-related microbiome changes compared to wildtype (WT) mice, including an increase in Bacteroides, which were normalized by CR. Specific gut microbiota changes were linked to Aβ levels, with greater effects in females than in males. In the gut, Tg2576 female mice had an enhanced intestinal inflammatory transcriptional profile, which was reversed by CR. Furthermore, we demonstrate that Bacteroides colonization exacerbates Aβ deposition, which may be a mechanism whereby the gut impacts AD pathogenesis. These results suggest that long-term CR may alter the gut environment and prevent the expansion of microbes that contribute to age-related cognitive decline.
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spelling pubmed-68844942019-12-06 Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice Cox, Laura M. Schafer, Marissa J. Sohn, Jiho Vincentini, Julia Weiner, Howard L. Ginsberg, Stephen D. Blaser, Martin J. Sci Rep Article Alzheimer’s disease (AD) affects an estimated 5.8 million Americans, and advanced age is the greatest risk factor. AD patients have altered intestinal microbiota. Accordingly, depleting intestinal microbiota in AD animal models reduces amyloid-beta (Aβ) plaque deposition. Age-related changes in the microbiota contribute to immunologic and physiologic decline. Translationally relevant dietary manipulations may be an effective approach to slow microbiota changes during aging. We previously showed that calorie restriction (CR) reduced brain Aβ deposition in the well-established Tg2576 mouse model of AD. Presently, we investigated whether CR alters the microbiome during aging. We found that female Tg2576 mice have more substantial age-related microbiome changes compared to wildtype (WT) mice, including an increase in Bacteroides, which were normalized by CR. Specific gut microbiota changes were linked to Aβ levels, with greater effects in females than in males. In the gut, Tg2576 female mice had an enhanced intestinal inflammatory transcriptional profile, which was reversed by CR. Furthermore, we demonstrate that Bacteroides colonization exacerbates Aβ deposition, which may be a mechanism whereby the gut impacts AD pathogenesis. These results suggest that long-term CR may alter the gut environment and prevent the expansion of microbes that contribute to age-related cognitive decline. Nature Publishing Group UK 2019-11-29 /pmc/articles/PMC6884494/ /pubmed/31784610 http://dx.doi.org/10.1038/s41598-019-54187-x Text en © The Author(s) 2019 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/.
spellingShingle Article
Cox, Laura M.
Schafer, Marissa J.
Sohn, Jiho
Vincentini, Julia
Weiner, Howard L.
Ginsberg, Stephen D.
Blaser, Martin J.
Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice
title Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice
title_full Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice
title_fullStr Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice
title_full_unstemmed Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice
title_short Calorie restriction slows age-related microbiota changes in an Alzheimer’s disease model in female mice
title_sort calorie restriction slows age-related microbiota changes in an alzheimer’s disease model in female mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6884494/
https://www.ncbi.nlm.nih.gov/pubmed/31784610
http://dx.doi.org/10.1038/s41598-019-54187-x
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