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Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex

It is well-known that antibiotics affect commensal gut bacteria; however, only recently evidence accumulated that gut microbiota (GM) can influence the central nervous system functions. Preclinical animal studies have repeatedly highlighted the effects of antibiotics on brain activity; however, tran...

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Autores principales: Sometti, Davide, Ballan, Chiara, Wang, Huiying, Braun, Christoph, Enck, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904800/
https://www.ncbi.nlm.nih.gov/pubmed/33627763
http://dx.doi.org/10.1038/s41598-021-83994-4
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author Sometti, Davide
Ballan, Chiara
Wang, Huiying
Braun, Christoph
Enck, Paul
author_facet Sometti, Davide
Ballan, Chiara
Wang, Huiying
Braun, Christoph
Enck, Paul
author_sort Sometti, Davide
collection PubMed
description It is well-known that antibiotics affect commensal gut bacteria; however, only recently evidence accumulated that gut microbiota (GM) can influence the central nervous system functions. Preclinical animal studies have repeatedly highlighted the effects of antibiotics on brain activity; however, translational studies in humans are still missing. Here, we present a randomized, double-blind, placebo-controlled study investigating the effects of 7 days intake of Rifaximin (non-absorbable antibiotic) on functional brain connectivity (fc) using magnetoencephalography. Sixteen healthy volunteers were tested before and after the treatment, during resting state (rs), and during a social stressor paradigm (Cyberball game—CBG), designed to elicit feelings of exclusion. Results confirm the hypothesis of an involvement of the insular cortex as a common node of different functional networks, thus suggesting its potential role as a central mediator of cortical fc alterations, following modifications of GM. Also, the Rifaximin group displayed lower connectivity in slow and fast beta bands (15 and 25 Hz) during rest, and higher connectivity in theta (7 Hz) during the inclusion condition of the CBG, compared with controls. Altogether these results indicate a modulation of Rifaximin on frequency-specific functional connectivity that could involve cognitive flexibility and memory processing.
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spelling pubmed-79048002021-02-25 Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex Sometti, Davide Ballan, Chiara Wang, Huiying Braun, Christoph Enck, Paul Sci Rep Article It is well-known that antibiotics affect commensal gut bacteria; however, only recently evidence accumulated that gut microbiota (GM) can influence the central nervous system functions. Preclinical animal studies have repeatedly highlighted the effects of antibiotics on brain activity; however, translational studies in humans are still missing. Here, we present a randomized, double-blind, placebo-controlled study investigating the effects of 7 days intake of Rifaximin (non-absorbable antibiotic) on functional brain connectivity (fc) using magnetoencephalography. Sixteen healthy volunteers were tested before and after the treatment, during resting state (rs), and during a social stressor paradigm (Cyberball game—CBG), designed to elicit feelings of exclusion. Results confirm the hypothesis of an involvement of the insular cortex as a common node of different functional networks, thus suggesting its potential role as a central mediator of cortical fc alterations, following modifications of GM. Also, the Rifaximin group displayed lower connectivity in slow and fast beta bands (15 and 25 Hz) during rest, and higher connectivity in theta (7 Hz) during the inclusion condition of the CBG, compared with controls. Altogether these results indicate a modulation of Rifaximin on frequency-specific functional connectivity that could involve cognitive flexibility and memory processing. Nature Publishing Group UK 2021-02-24 /pmc/articles/PMC7904800/ /pubmed/33627763 http://dx.doi.org/10.1038/s41598-021-83994-4 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sometti, Davide
Ballan, Chiara
Wang, Huiying
Braun, Christoph
Enck, Paul
Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex
title Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex
title_full Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex
title_fullStr Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex
title_full_unstemmed Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex
title_short Effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex
title_sort effects of the antibiotic rifaximin on cortical functional connectivity are mediated through insular cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904800/
https://www.ncbi.nlm.nih.gov/pubmed/33627763
http://dx.doi.org/10.1038/s41598-021-83994-4
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