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Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice

Several studies revealed that substantial artificial changes in the gut microbiota resulted in modification of hepatic cytochrome P450 3a (Cyp3a) in mice. Consequently, we hypothesized that “normal” variation of the gut microbiota might also alter hepatic Cyp activity and lead to individual differen...

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Autores principales: Togao, Masao, Tajima, Shinnosuke, Kurakawa, Takashi, Wagai, Gaku, Otsuka, Jun, Kado, Shoichi, Kawakami, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573722/
https://www.ncbi.nlm.nih.gov/pubmed/34747570
http://dx.doi.org/10.1002/prp2.893
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author Togao, Masao
Tajima, Shinnosuke
Kurakawa, Takashi
Wagai, Gaku
Otsuka, Jun
Kado, Shoichi
Kawakami, Koji
author_facet Togao, Masao
Tajima, Shinnosuke
Kurakawa, Takashi
Wagai, Gaku
Otsuka, Jun
Kado, Shoichi
Kawakami, Koji
author_sort Togao, Masao
collection PubMed
description Several studies revealed that substantial artificial changes in the gut microbiota resulted in modification of hepatic cytochrome P450 3a (Cyp3a) in mice. Consequently, we hypothesized that “normal” variation of the gut microbiota might also alter hepatic Cyp activity and lead to individual differences in drug metabolism. Therefore, this study investigated the effects of normal gut microbiota variation on hepatic Cyp activity under the same genetic and environmental conditions using ex‐germ‐free mice. Using the feces of three breeder BALB/c mice (Jcl, Slc, and Crj), germ‐free BALB/cYit mice were conventionalized (Yit‐Jcl, Yit‐Slc, and Yit‐Crj). The gut microbiota composition and hepatic Cyp activity of these donors and recipients were evaluated. 16S rRNA sequencing revealed clear differences of the gut microbiota among donors and among recipients. Cyp3a activity was significantly higher in Slc mice than in Jcl and Crj mice. Notably, among recipients, Cyp3a activity was significantly higher in Yit‐Slc and Yit‐Crj mice than in Yit‐Jcl mice. Cyp2b activity was significantly higher in Slc mice than in Jcl and Crj mice. Cyp2b activity was significantly higher in Yit‐Slc mice than in Yit‐Jcl mice. Additionally, in correlation analysis, some genera displayed significant positive or negative correlations with Cyp activity, particular the strong positive correlation between Clostridium sensu stricto 1 with Cyp3a activity. In conclusion, this study demonstrated that normal variation of the gut microbiota affected hepatic Cyp3a and Cyp2b activity, which might result in individual differences of drug metabolism.
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spelling pubmed-85737222021-11-10 Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice Togao, Masao Tajima, Shinnosuke Kurakawa, Takashi Wagai, Gaku Otsuka, Jun Kado, Shoichi Kawakami, Koji Pharmacol Res Perspect Original Articles Several studies revealed that substantial artificial changes in the gut microbiota resulted in modification of hepatic cytochrome P450 3a (Cyp3a) in mice. Consequently, we hypothesized that “normal” variation of the gut microbiota might also alter hepatic Cyp activity and lead to individual differences in drug metabolism. Therefore, this study investigated the effects of normal gut microbiota variation on hepatic Cyp activity under the same genetic and environmental conditions using ex‐germ‐free mice. Using the feces of three breeder BALB/c mice (Jcl, Slc, and Crj), germ‐free BALB/cYit mice were conventionalized (Yit‐Jcl, Yit‐Slc, and Yit‐Crj). The gut microbiota composition and hepatic Cyp activity of these donors and recipients were evaluated. 16S rRNA sequencing revealed clear differences of the gut microbiota among donors and among recipients. Cyp3a activity was significantly higher in Slc mice than in Jcl and Crj mice. Notably, among recipients, Cyp3a activity was significantly higher in Yit‐Slc and Yit‐Crj mice than in Yit‐Jcl mice. Cyp2b activity was significantly higher in Slc mice than in Jcl and Crj mice. Cyp2b activity was significantly higher in Yit‐Slc mice than in Yit‐Jcl mice. Additionally, in correlation analysis, some genera displayed significant positive or negative correlations with Cyp activity, particular the strong positive correlation between Clostridium sensu stricto 1 with Cyp3a activity. In conclusion, this study demonstrated that normal variation of the gut microbiota affected hepatic Cyp3a and Cyp2b activity, which might result in individual differences of drug metabolism. John Wiley and Sons Inc. 2021-11-08 /pmc/articles/PMC8573722/ /pubmed/34747570 http://dx.doi.org/10.1002/prp2.893 Text en © 2021 The Authors. Pharmacology Research & Perspectives published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Togao, Masao
Tajima, Shinnosuke
Kurakawa, Takashi
Wagai, Gaku
Otsuka, Jun
Kado, Shoichi
Kawakami, Koji
Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice
title Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice
title_full Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice
title_fullStr Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice
title_full_unstemmed Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice
title_short Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice
title_sort normal variation of the gut microbiota affects hepatic cytochrome p450 activity in mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573722/
https://www.ncbi.nlm.nih.gov/pubmed/34747570
http://dx.doi.org/10.1002/prp2.893
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