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The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice

The gut microbiota is involved in a number of different metabolic processes of the host organism, including the metabolism of xenobiotics. In our study, we focused on liver cytochromes P450 (CYPs), which can metabolize a wide range of exo- and endogenous molecules. We studied changes in mRNA express...

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Autores principales: Zemanová, Nina, Anzenbacher, Pavel, Zapletalová, Iveta, Jourová, Lenka, Hermanová, Petra, Hudcovic, Tomáš, Kozáková, Hana, Vodička, Martin, Pácha, Jiří, Anzenbacherová, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244717/
https://www.ncbi.nlm.nih.gov/pubmed/32444678
http://dx.doi.org/10.1038/s41598-020-65595-9
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author Zemanová, Nina
Anzenbacher, Pavel
Zapletalová, Iveta
Jourová, Lenka
Hermanová, Petra
Hudcovic, Tomáš
Kozáková, Hana
Vodička, Martin
Pácha, Jiří
Anzenbacherová, Eva
author_facet Zemanová, Nina
Anzenbacher, Pavel
Zapletalová, Iveta
Jourová, Lenka
Hermanová, Petra
Hudcovic, Tomáš
Kozáková, Hana
Vodička, Martin
Pácha, Jiří
Anzenbacherová, Eva
author_sort Zemanová, Nina
collection PubMed
description The gut microbiota is involved in a number of different metabolic processes of the host organism, including the metabolism of xenobiotics. In our study, we focused on liver cytochromes P450 (CYPs), which can metabolize a wide range of exo- and endogenous molecules. We studied changes in mRNA expression and CYP enzyme activities, as well as the mRNA expression of transcription factors that have an important role in CYP expression, all in stressed germ-free (GF) and stressed specific-pathogen-free (SPF) mice. Besides the presence of the gut microbiota, we looked at the difference between acute and chronic stress. Our results show that stress has an impact on CYP mRNA expression, but it is mainly chronic stress that has a significant effect on enzyme activities along with the gut microbiome. In acutely stressed mice, we observed significant changes at the mRNA level, however, the corresponding enzyme activities were not influenced. Our study suggests an important role of the gut microbiota along with chronic psychosocial stress in the expression and activity of CYPs, which can potentially lead to less effective drug metabolism and, as a result, a harmful impact on the organism.
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spelling pubmed-72447172020-05-30 The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice Zemanová, Nina Anzenbacher, Pavel Zapletalová, Iveta Jourová, Lenka Hermanová, Petra Hudcovic, Tomáš Kozáková, Hana Vodička, Martin Pácha, Jiří Anzenbacherová, Eva Sci Rep Article The gut microbiota is involved in a number of different metabolic processes of the host organism, including the metabolism of xenobiotics. In our study, we focused on liver cytochromes P450 (CYPs), which can metabolize a wide range of exo- and endogenous molecules. We studied changes in mRNA expression and CYP enzyme activities, as well as the mRNA expression of transcription factors that have an important role in CYP expression, all in stressed germ-free (GF) and stressed specific-pathogen-free (SPF) mice. Besides the presence of the gut microbiota, we looked at the difference between acute and chronic stress. Our results show that stress has an impact on CYP mRNA expression, but it is mainly chronic stress that has a significant effect on enzyme activities along with the gut microbiome. In acutely stressed mice, we observed significant changes at the mRNA level, however, the corresponding enzyme activities were not influenced. Our study suggests an important role of the gut microbiota along with chronic psychosocial stress in the expression and activity of CYPs, which can potentially lead to less effective drug metabolism and, as a result, a harmful impact on the organism. Nature Publishing Group UK 2020-05-22 /pmc/articles/PMC7244717/ /pubmed/32444678 http://dx.doi.org/10.1038/s41598-020-65595-9 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
Zemanová, Nina
Anzenbacher, Pavel
Zapletalová, Iveta
Jourová, Lenka
Hermanová, Petra
Hudcovic, Tomáš
Kozáková, Hana
Vodička, Martin
Pácha, Jiří
Anzenbacherová, Eva
The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice
title The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice
title_full The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice
title_fullStr The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice
title_full_unstemmed The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice
title_short The role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice
title_sort role of the microbiome and psychosocial stress in the expression and activity of drug metabolizing enzymes in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244717/
https://www.ncbi.nlm.nih.gov/pubmed/32444678
http://dx.doi.org/10.1038/s41598-020-65595-9
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