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Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice
BACKGROUND: Influenza A virus infection due to drug resistance and side effects of the conventional antiviral drugs yet remains a serious public health threat for humans and animals. Forsythiaside A is an effective ingredient isolated from the Chinese herbal medicine forsythia. It has various pharma...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214192/ https://www.ncbi.nlm.nih.gov/pubmed/35733131 http://dx.doi.org/10.1186/s12906-022-03644-8 |
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author | Zheng, Xiao Chen, Ziqi Shi, Shanshan Yan, Huijun Zhou, Junmei Jiang, Lifang Wang, Hongli Hou, Guanghui Jiang, Zhenyou |
author_facet | Zheng, Xiao Chen, Ziqi Shi, Shanshan Yan, Huijun Zhou, Junmei Jiang, Lifang Wang, Hongli Hou, Guanghui Jiang, Zhenyou |
author_sort | Zheng, Xiao |
collection | PubMed |
description | BACKGROUND: Influenza A virus infection due to drug resistance and side effects of the conventional antiviral drugs yet remains a serious public health threat for humans and animals. Forsythiaside A is an effective ingredient isolated from the Chinese herbal medicine forsythia. It has various pharmacological effects and has a good therapeutic effect against a variety of infectious diseases. This study aimed to further explore the immunological mechanism of Forsythiaside A in the treatment of influenza virus-infected mice and its effect on the Toll-like receptor 7 (TLR7) signaling pathway in the lungs of these mice. METHODS: C57/BL6J mice and TLR7(−/−) mice were infected with the FM1 strains (H1N1 and A/FM/1/4) of the Influenza A virus. Each group of experimental mice were divided into the mock, virus, oseltamivir, and Forsythiaside A groups. Weight change, lung index change, and the mRNA and protein expression levels of key factors in the TLR7 signaling pathway were detected. Flow cytometry was used to detect the changes in the Th1/Th2 and Th17/Treg ratios. RESULTS: After infection with the Influenza A virus, the weight loss of C57/BL6J mice treated with forsythoside A and oseltamivir decreased, and the pathological tissue sections showed that the inflammatory damage was reduced. The expression levels of the key factors, TLR7, myeloid differentiation factor 88(Myd88), and nuclear factor-kappa B (NF-κB) in the TLR7 signaling pathway were significantly reduced. Flow cytometry showed that Th1/Th2 and Th17/Treg ratios decreased after Forsythiaside A treatment. In the TLR7(−/−) mice, there was no significant change after Forsythiaside A treatment in the virus group. CONCLUSIONS: Forsythiaside A affects the TLR7 signaling pathway in mouse lung immune cells and reduces the inflammatory response caused by the Influenza A virus FM1 strain in mouse lungs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-022-03644-8. |
format | Online Article Text |
id | pubmed-9214192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92141922022-06-22 Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice Zheng, Xiao Chen, Ziqi Shi, Shanshan Yan, Huijun Zhou, Junmei Jiang, Lifang Wang, Hongli Hou, Guanghui Jiang, Zhenyou BMC Complement Med Ther Research BACKGROUND: Influenza A virus infection due to drug resistance and side effects of the conventional antiviral drugs yet remains a serious public health threat for humans and animals. Forsythiaside A is an effective ingredient isolated from the Chinese herbal medicine forsythia. It has various pharmacological effects and has a good therapeutic effect against a variety of infectious diseases. This study aimed to further explore the immunological mechanism of Forsythiaside A in the treatment of influenza virus-infected mice and its effect on the Toll-like receptor 7 (TLR7) signaling pathway in the lungs of these mice. METHODS: C57/BL6J mice and TLR7(−/−) mice were infected with the FM1 strains (H1N1 and A/FM/1/4) of the Influenza A virus. Each group of experimental mice were divided into the mock, virus, oseltamivir, and Forsythiaside A groups. Weight change, lung index change, and the mRNA and protein expression levels of key factors in the TLR7 signaling pathway were detected. Flow cytometry was used to detect the changes in the Th1/Th2 and Th17/Treg ratios. RESULTS: After infection with the Influenza A virus, the weight loss of C57/BL6J mice treated with forsythoside A and oseltamivir decreased, and the pathological tissue sections showed that the inflammatory damage was reduced. The expression levels of the key factors, TLR7, myeloid differentiation factor 88(Myd88), and nuclear factor-kappa B (NF-κB) in the TLR7 signaling pathway were significantly reduced. Flow cytometry showed that Th1/Th2 and Th17/Treg ratios decreased after Forsythiaside A treatment. In the TLR7(−/−) mice, there was no significant change after Forsythiaside A treatment in the virus group. CONCLUSIONS: Forsythiaside A affects the TLR7 signaling pathway in mouse lung immune cells and reduces the inflammatory response caused by the Influenza A virus FM1 strain in mouse lungs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-022-03644-8. BioMed Central 2022-06-22 /pmc/articles/PMC9214192/ /pubmed/35733131 http://dx.doi.org/10.1186/s12906-022-03644-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zheng, Xiao Chen, Ziqi Shi, Shanshan Yan, Huijun Zhou, Junmei Jiang, Lifang Wang, Hongli Hou, Guanghui Jiang, Zhenyou Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice |
title | Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice |
title_full | Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice |
title_fullStr | Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice |
title_full_unstemmed | Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice |
title_short | Forsythiaside A improves Influenza A virus infection through TLR7 signaling pathway in the lungs of mice |
title_sort | forsythiaside a improves influenza a virus infection through tlr7 signaling pathway in the lungs of mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214192/ https://www.ncbi.nlm.nih.gov/pubmed/35733131 http://dx.doi.org/10.1186/s12906-022-03644-8 |
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