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Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep

Dietary prebiotics produce favorable changes in the commensal gut microbiome and reduce host vulnerability to stress-induced disruptions in complex behaviors such as sleep. The mechanisms for how prebiotics modulate stress physiology remain unclear; however, emerging evidence suggests that gut micro...

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Autores principales: Thompson, Robert S., Vargas, Fernando, Dorrestein, Pieter C., Chichlowski, Maciej, Berg, Brian M., Fleshner, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051969/
https://www.ncbi.nlm.nih.gov/pubmed/32123201
http://dx.doi.org/10.1038/s41598-020-60679-y
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author Thompson, Robert S.
Vargas, Fernando
Dorrestein, Pieter C.
Chichlowski, Maciej
Berg, Brian M.
Fleshner, Monika
author_facet Thompson, Robert S.
Vargas, Fernando
Dorrestein, Pieter C.
Chichlowski, Maciej
Berg, Brian M.
Fleshner, Monika
author_sort Thompson, Robert S.
collection PubMed
description Dietary prebiotics produce favorable changes in the commensal gut microbiome and reduce host vulnerability to stress-induced disruptions in complex behaviors such as sleep. The mechanisms for how prebiotics modulate stress physiology remain unclear; however, emerging evidence suggests that gut microbes and their metabolites may play a role. This study tested if stress and/or dietary prebiotics (Test diet) alter the fecal metabolome; and explored if these changes were related to sleep and/or gut microbial alpha diversity. Male F344 rats on either Test or Control diet were instrumented for electroencephalography biotelemetry measures of sleep/wake. After 5 weeks on diet, rats were either stressed or remained in home cages. Based on untargeted mass spectrometry and 16S rRNA gene sequencing, both stress and Test diet altered the fecal metabolome/microbiome. In addition, Test diet prevented the stress-induced reduction in microbial alpha diversity based on PD_Whole_Tree, which has been previously published. Network propagation analysis revealed that stress increased members of the neuroactive steroidal pregnane molecular family; and that Test diet reduced this effect. We also discovered links between sleep, alpha diversity, and pyrimidine, secondary bile acid, and neuroactive glucocorticoid/pregnanolone-type steroidal metabolites. These results reveal novel microbial-dependent metabolites that may modulate stress physiology and sleep.
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spelling pubmed-70519692020-03-06 Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep Thompson, Robert S. Vargas, Fernando Dorrestein, Pieter C. Chichlowski, Maciej Berg, Brian M. Fleshner, Monika Sci Rep Article Dietary prebiotics produce favorable changes in the commensal gut microbiome and reduce host vulnerability to stress-induced disruptions in complex behaviors such as sleep. The mechanisms for how prebiotics modulate stress physiology remain unclear; however, emerging evidence suggests that gut microbes and their metabolites may play a role. This study tested if stress and/or dietary prebiotics (Test diet) alter the fecal metabolome; and explored if these changes were related to sleep and/or gut microbial alpha diversity. Male F344 rats on either Test or Control diet were instrumented for electroencephalography biotelemetry measures of sleep/wake. After 5 weeks on diet, rats were either stressed or remained in home cages. Based on untargeted mass spectrometry and 16S rRNA gene sequencing, both stress and Test diet altered the fecal metabolome/microbiome. In addition, Test diet prevented the stress-induced reduction in microbial alpha diversity based on PD_Whole_Tree, which has been previously published. Network propagation analysis revealed that stress increased members of the neuroactive steroidal pregnane molecular family; and that Test diet reduced this effect. We also discovered links between sleep, alpha diversity, and pyrimidine, secondary bile acid, and neuroactive glucocorticoid/pregnanolone-type steroidal metabolites. These results reveal novel microbial-dependent metabolites that may modulate stress physiology and sleep. Nature Publishing Group UK 2020-03-02 /pmc/articles/PMC7051969/ /pubmed/32123201 http://dx.doi.org/10.1038/s41598-020-60679-y Text en © The Author(s) 2020 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
Thompson, Robert S.
Vargas, Fernando
Dorrestein, Pieter C.
Chichlowski, Maciej
Berg, Brian M.
Fleshner, Monika
Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep
title Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep
title_full Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep
title_fullStr Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep
title_full_unstemmed Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep
title_short Dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep
title_sort dietary prebiotics alter novel microbial dependent fecal metabolites that improve sleep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051969/
https://www.ncbi.nlm.nih.gov/pubmed/32123201
http://dx.doi.org/10.1038/s41598-020-60679-y
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