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Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease

Mechanisms linking intestinal bacteria and neurodegenerative diseases such as Alzheimer’s disease (AD) are still unclear. We hypothesized that intestinal dysbiosis might potentiate AD, and manipulating the microbiome to promote intestinal eubiosis and immune homeostasis may improve AD-related brain...

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Autores principales: Kaur, Harpreet, Nookala, Suba, Singh, Surjeet, Mukundan, Santhosh, Nagamoto-Combs, Kumi, Combs, Colin Kelly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469717/
https://www.ncbi.nlm.nih.gov/pubmed/34572019
http://dx.doi.org/10.3390/cells10092370
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author Kaur, Harpreet
Nookala, Suba
Singh, Surjeet
Mukundan, Santhosh
Nagamoto-Combs, Kumi
Combs, Colin Kelly
author_facet Kaur, Harpreet
Nookala, Suba
Singh, Surjeet
Mukundan, Santhosh
Nagamoto-Combs, Kumi
Combs, Colin Kelly
author_sort Kaur, Harpreet
collection PubMed
description Mechanisms linking intestinal bacteria and neurodegenerative diseases such as Alzheimer’s disease (AD) are still unclear. We hypothesized that intestinal dysbiosis might potentiate AD, and manipulating the microbiome to promote intestinal eubiosis and immune homeostasis may improve AD-related brain changes. This study assessed sex differences in the effects of oral probiotic, antibiotics, and synbiotic treatments in the App(NL-G-F) mouse model of AD. The fecal microbiome demonstrated significant correlations between bacterial genera in App(NL-G-F) mice and Aβ plaque load, gliosis, and memory performance. Female and not male App(NL-G-F) mice fed probiotic but not synbiotic exhibited a decrease in Aβ plaques, microgliosis, brain TNF-α, and memory improvement compared to no treatment controls. Although antibiotics treatment did not produce these multiple changes in brain cytokines, memory, or gliosis, it did decrease Aβ plaque load and colon cytokines in App(NL-G-F) males. The intestinal cytokine milieu and splenocyte phenotype of female but not male App(NL-G-F) mice indicated a modest proinflammatory innate response following probiotic treatment compared to controls, with an adaptive response following antibiotics treatment in male App(NL-G-F) mice. Overall, these results demonstrate the beneficial effects of probiotic only in App(NL-G-F) females, with minimal benefits of antibiotics or synbiotic feeding in male or female mice.
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spelling pubmed-84697172021-09-27 Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease Kaur, Harpreet Nookala, Suba Singh, Surjeet Mukundan, Santhosh Nagamoto-Combs, Kumi Combs, Colin Kelly Cells Article Mechanisms linking intestinal bacteria and neurodegenerative diseases such as Alzheimer’s disease (AD) are still unclear. We hypothesized that intestinal dysbiosis might potentiate AD, and manipulating the microbiome to promote intestinal eubiosis and immune homeostasis may improve AD-related brain changes. This study assessed sex differences in the effects of oral probiotic, antibiotics, and synbiotic treatments in the App(NL-G-F) mouse model of AD. The fecal microbiome demonstrated significant correlations between bacterial genera in App(NL-G-F) mice and Aβ plaque load, gliosis, and memory performance. Female and not male App(NL-G-F) mice fed probiotic but not synbiotic exhibited a decrease in Aβ plaques, microgliosis, brain TNF-α, and memory improvement compared to no treatment controls. Although antibiotics treatment did not produce these multiple changes in brain cytokines, memory, or gliosis, it did decrease Aβ plaque load and colon cytokines in App(NL-G-F) males. The intestinal cytokine milieu and splenocyte phenotype of female but not male App(NL-G-F) mice indicated a modest proinflammatory innate response following probiotic treatment compared to controls, with an adaptive response following antibiotics treatment in male App(NL-G-F) mice. Overall, these results demonstrate the beneficial effects of probiotic only in App(NL-G-F) females, with minimal benefits of antibiotics or synbiotic feeding in male or female mice. MDPI 2021-09-09 /pmc/articles/PMC8469717/ /pubmed/34572019 http://dx.doi.org/10.3390/cells10092370 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kaur, Harpreet
Nookala, Suba
Singh, Surjeet
Mukundan, Santhosh
Nagamoto-Combs, Kumi
Combs, Colin Kelly
Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease
title Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease
title_full Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease
title_fullStr Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease
title_full_unstemmed Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease
title_short Sex-Dependent Effects of Intestinal Microbiome Manipulation in a Mouse Model of Alzheimer’s Disease
title_sort sex-dependent effects of intestinal microbiome manipulation in a mouse model of alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469717/
https://www.ncbi.nlm.nih.gov/pubmed/34572019
http://dx.doi.org/10.3390/cells10092370
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