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The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia
The gut microbiome has been implicated as a key regulator of brain function in health and disease. But the impact of gut microbiota on functional brain connectivity is unknown. We used resting-state functional magnetic resonance imaging in germ-free and normally colonized mice under naive conditions...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479691/ https://www.ncbi.nlm.nih.gov/pubmed/34622150 http://dx.doi.org/10.1016/j.isci.2021.103095 |
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author | Aswendt, Markus Green, Claudia Sadler, Rebecca Llovera, Gemma Dzikowski, Lauren Heindl, Steffanie Gomez de Agüero, Mercedes Diedenhofen, Michael Vogel, Stefanie Wieters, Frederique Wiedermann, Dirk Liesz, Arthur Hoehn, Mathias |
author_facet | Aswendt, Markus Green, Claudia Sadler, Rebecca Llovera, Gemma Dzikowski, Lauren Heindl, Steffanie Gomez de Agüero, Mercedes Diedenhofen, Michael Vogel, Stefanie Wieters, Frederique Wiedermann, Dirk Liesz, Arthur Hoehn, Mathias |
author_sort | Aswendt, Markus |
collection | PubMed |
description | The gut microbiome has been implicated as a key regulator of brain function in health and disease. But the impact of gut microbiota on functional brain connectivity is unknown. We used resting-state functional magnetic resonance imaging in germ-free and normally colonized mice under naive conditions and after ischemic stroke. We observed a strong, brain-wide increase of functional connectivity in germ-free animals. Graph theoretical analysis revealed significant higher values in germ-free animals, indicating a stronger and denser global network but with less structural organization. Breakdown of network function after stroke equally affected germ-free and colonized mice. Results from histological analyses showed changes in dendritic spine densities, as well as an immature microglial phenotype, indicating impaired microglia-neuron interaction in germ-free mice as potential cause of this phenomenon. These results demonstrate the substantial impact of bacterial colonization on brain-wide function and extend our so far mainly (sub) cellular understanding of the gut-brain axis. |
format | Online Article Text |
id | pubmed-8479691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-84796912021-10-06 The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia Aswendt, Markus Green, Claudia Sadler, Rebecca Llovera, Gemma Dzikowski, Lauren Heindl, Steffanie Gomez de Agüero, Mercedes Diedenhofen, Michael Vogel, Stefanie Wieters, Frederique Wiedermann, Dirk Liesz, Arthur Hoehn, Mathias iScience Article The gut microbiome has been implicated as a key regulator of brain function in health and disease. But the impact of gut microbiota on functional brain connectivity is unknown. We used resting-state functional magnetic resonance imaging in germ-free and normally colonized mice under naive conditions and after ischemic stroke. We observed a strong, brain-wide increase of functional connectivity in germ-free animals. Graph theoretical analysis revealed significant higher values in germ-free animals, indicating a stronger and denser global network but with less structural organization. Breakdown of network function after stroke equally affected germ-free and colonized mice. Results from histological analyses showed changes in dendritic spine densities, as well as an immature microglial phenotype, indicating impaired microglia-neuron interaction in germ-free mice as potential cause of this phenomenon. These results demonstrate the substantial impact of bacterial colonization on brain-wide function and extend our so far mainly (sub) cellular understanding of the gut-brain axis. Elsevier 2021-09-09 /pmc/articles/PMC8479691/ /pubmed/34622150 http://dx.doi.org/10.1016/j.isci.2021.103095 Text en © 2021. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Aswendt, Markus Green, Claudia Sadler, Rebecca Llovera, Gemma Dzikowski, Lauren Heindl, Steffanie Gomez de Agüero, Mercedes Diedenhofen, Michael Vogel, Stefanie Wieters, Frederique Wiedermann, Dirk Liesz, Arthur Hoehn, Mathias The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia |
title | The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia |
title_full | The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia |
title_fullStr | The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia |
title_full_unstemmed | The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia |
title_short | The gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia |
title_sort | gut microbiota modulates brain network connectivity under physiological conditions and after acute brain ischemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479691/ https://www.ncbi.nlm.nih.gov/pubmed/34622150 http://dx.doi.org/10.1016/j.isci.2021.103095 |
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