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Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection
Maoto, a traditional kampo medicine, has been clinically prescribed for influenza infection and is reported to relieve symptoms and tissue damage. In this study, we evaluated the effects of maoto as an herbal multi-compound medicine on host responses in a mouse model of influenza infection. On the f...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896050/ https://www.ncbi.nlm.nih.gov/pubmed/33608574 http://dx.doi.org/10.1038/s41598-021-82707-1 |
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author | Nishi, Akinori Kaifuchi, Noriko Shimobori, Chika Ohbuchi, Katsuya Iizuka, Seiichi Sugiyama, Aiko Ogura, Keisuke Yamamoto, Masahiro Kuroki, Haruo Nabeshima, Shigeki Yachie, Ayako Matsuoka, Yukiko Kitano, Hiroaki |
author_facet | Nishi, Akinori Kaifuchi, Noriko Shimobori, Chika Ohbuchi, Katsuya Iizuka, Seiichi Sugiyama, Aiko Ogura, Keisuke Yamamoto, Masahiro Kuroki, Haruo Nabeshima, Shigeki Yachie, Ayako Matsuoka, Yukiko Kitano, Hiroaki |
author_sort | Nishi, Akinori |
collection | PubMed |
description | Maoto, a traditional kampo medicine, has been clinically prescribed for influenza infection and is reported to relieve symptoms and tissue damage. In this study, we evaluated the effects of maoto as an herbal multi-compound medicine on host responses in a mouse model of influenza infection. On the fifth day of oral administration to mice intranasally infected with influenza virus [A/PR/8/34 (H1N1)], maoto significantly improved survival rate, decreased viral titer, and ameliorated the infection-induced phenotype as compared with control mice. Analysis of the lung and plasma transcriptome and lipid mediator metabolite profile showed that maoto altered the profile of lipid mediators derived from ω-6 and ω-3 fatty acids to restore a normal state, and significantly up-regulated the expression of macrophage- and T-cell-related genes. Collectively, these results suggest that maoto regulates the host’s inflammatory response by altering the lipid mediator profile and thereby ameliorating the symptoms of influenza. |
format | Online Article Text |
id | pubmed-7896050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78960502021-02-24 Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection Nishi, Akinori Kaifuchi, Noriko Shimobori, Chika Ohbuchi, Katsuya Iizuka, Seiichi Sugiyama, Aiko Ogura, Keisuke Yamamoto, Masahiro Kuroki, Haruo Nabeshima, Shigeki Yachie, Ayako Matsuoka, Yukiko Kitano, Hiroaki Sci Rep Article Maoto, a traditional kampo medicine, has been clinically prescribed for influenza infection and is reported to relieve symptoms and tissue damage. In this study, we evaluated the effects of maoto as an herbal multi-compound medicine on host responses in a mouse model of influenza infection. On the fifth day of oral administration to mice intranasally infected with influenza virus [A/PR/8/34 (H1N1)], maoto significantly improved survival rate, decreased viral titer, and ameliorated the infection-induced phenotype as compared with control mice. Analysis of the lung and plasma transcriptome and lipid mediator metabolite profile showed that maoto altered the profile of lipid mediators derived from ω-6 and ω-3 fatty acids to restore a normal state, and significantly up-regulated the expression of macrophage- and T-cell-related genes. Collectively, these results suggest that maoto regulates the host’s inflammatory response by altering the lipid mediator profile and thereby ameliorating the symptoms of influenza. Nature Publishing Group UK 2021-02-19 /pmc/articles/PMC7896050/ /pubmed/33608574 http://dx.doi.org/10.1038/s41598-021-82707-1 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 Nishi, Akinori Kaifuchi, Noriko Shimobori, Chika Ohbuchi, Katsuya Iizuka, Seiichi Sugiyama, Aiko Ogura, Keisuke Yamamoto, Masahiro Kuroki, Haruo Nabeshima, Shigeki Yachie, Ayako Matsuoka, Yukiko Kitano, Hiroaki Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection |
title | Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection |
title_full | Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection |
title_fullStr | Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection |
title_full_unstemmed | Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection |
title_short | Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection |
title_sort | effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896050/ https://www.ncbi.nlm.nih.gov/pubmed/33608574 http://dx.doi.org/10.1038/s41598-021-82707-1 |
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