Cargando…
Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway
ETHNOPHARMACOLOGICAL RELEVANCE: Acute lung injury (ALI) is a common manifestation of COVID-19. Xuanfei Baidu Formula(XFBD) is used in China to treat mild or common damp-toxin obstructive pulmonary syndrome in COVID-19 patients. However, the active ingredients of XFBD have not been extensively studie...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562620/ https://www.ncbi.nlm.nih.gov/pubmed/36252879 http://dx.doi.org/10.1016/j.jep.2022.115833 |
_version_ | 1784808214071607296 |
---|---|
author | Zhu, Yanru Luo, Lifei Zhang, Meng Song, Xinbo Wang, Ping Zhang, Han Zhang, Jingze Liu, Dailin |
author_facet | Zhu, Yanru Luo, Lifei Zhang, Meng Song, Xinbo Wang, Ping Zhang, Han Zhang, Jingze Liu, Dailin |
author_sort | Zhu, Yanru |
collection | PubMed |
description | ETHNOPHARMACOLOGICAL RELEVANCE: Acute lung injury (ALI) is a common manifestation of COVID-19. Xuanfei Baidu Formula(XFBD) is used in China to treat mild or common damp-toxin obstructive pulmonary syndrome in COVID-19 patients. However, the active ingredients of XFBD have not been extensively studied, and its mechanism of action in the treatment of ALI is not well understood. AIM OF THE STUDY: The purpose of this study was to investigate the mechanism of action of XFBD in treating ALI in rats, by evaluating its active components. MATERIALS AND METHODS: Firstly, the chemical composition of XFBD was identified using ultra-high performance liquid chromatography with quadrupole time-of-flight mass spectrometry. The potential targets of XFBD for ALI treatment were predicted using network pharmacological analysis. Finally, the molecular mechanism of XFBD was validated using a RAW264.7 cell inflammation model and a mouse ALI model. RESULTS: A total of 113 compounds were identified in XFBD. Network pharmacology revealed 34 hub targets between the 113 compounds and ALI. The results of Kyoto Encyclopedia of Genes and Genomes and gene ontology analyses indicated that the NF-κB signaling pathway was the main pathway for XFBD in the treatment of ALI. We found that XFBD reduced proinflammatory factor levels in LPS-induced cellular models. By examining the lung wet/dry weight ratio and pathological sections in vivo, XFBD was found that XFBD could alleviate ALI. Immunohistochemistry results showed that XFBD inhibited ALI-induced increases in p-IKK, p–NF–κB p65, and iNOS proteins. In vitro experiments demonstrated that XFBD inhibited LPS-induced activation of the NF-κB pathway. CONCLUSION: This study identified the potential practical components of XFBD, combined with network pharmacology and experimental validation to demonstrate that XFBD can alleviate lung injury caused by ALI by inhibiting the NF-κB signaling pathway. |
format | Online Article Text |
id | pubmed-9562620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95626202022-10-16 Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway Zhu, Yanru Luo, Lifei Zhang, Meng Song, Xinbo Wang, Ping Zhang, Han Zhang, Jingze Liu, Dailin J Ethnopharmacol Article ETHNOPHARMACOLOGICAL RELEVANCE: Acute lung injury (ALI) is a common manifestation of COVID-19. Xuanfei Baidu Formula(XFBD) is used in China to treat mild or common damp-toxin obstructive pulmonary syndrome in COVID-19 patients. However, the active ingredients of XFBD have not been extensively studied, and its mechanism of action in the treatment of ALI is not well understood. AIM OF THE STUDY: The purpose of this study was to investigate the mechanism of action of XFBD in treating ALI in rats, by evaluating its active components. MATERIALS AND METHODS: Firstly, the chemical composition of XFBD was identified using ultra-high performance liquid chromatography with quadrupole time-of-flight mass spectrometry. The potential targets of XFBD for ALI treatment were predicted using network pharmacological analysis. Finally, the molecular mechanism of XFBD was validated using a RAW264.7 cell inflammation model and a mouse ALI model. RESULTS: A total of 113 compounds were identified in XFBD. Network pharmacology revealed 34 hub targets between the 113 compounds and ALI. The results of Kyoto Encyclopedia of Genes and Genomes and gene ontology analyses indicated that the NF-κB signaling pathway was the main pathway for XFBD in the treatment of ALI. We found that XFBD reduced proinflammatory factor levels in LPS-induced cellular models. By examining the lung wet/dry weight ratio and pathological sections in vivo, XFBD was found that XFBD could alleviate ALI. Immunohistochemistry results showed that XFBD inhibited ALI-induced increases in p-IKK, p–NF–κB p65, and iNOS proteins. In vitro experiments demonstrated that XFBD inhibited LPS-induced activation of the NF-κB pathway. CONCLUSION: This study identified the potential practical components of XFBD, combined with network pharmacology and experimental validation to demonstrate that XFBD can alleviate lung injury caused by ALI by inhibiting the NF-κB signaling pathway. Elsevier B.V. 2023-01-30 2022-10-14 /pmc/articles/PMC9562620/ /pubmed/36252879 http://dx.doi.org/10.1016/j.jep.2022.115833 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Zhu, Yanru Luo, Lifei Zhang, Meng Song, Xinbo Wang, Ping Zhang, Han Zhang, Jingze Liu, Dailin Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway |
title | Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway |
title_full | Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway |
title_fullStr | Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway |
title_full_unstemmed | Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway |
title_short | Xuanfei Baidu Formula attenuates LPS-induced acute lung injury by inhibiting the NF-κB signaling pathway |
title_sort | xuanfei baidu formula attenuates lps-induced acute lung injury by inhibiting the nf-κb signaling pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562620/ https://www.ncbi.nlm.nih.gov/pubmed/36252879 http://dx.doi.org/10.1016/j.jep.2022.115833 |
work_keys_str_mv | AT zhuyanru xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway AT luolifei xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway AT zhangmeng xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway AT songxinbo xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway AT wangping xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway AT zhanghan xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway AT zhangjingze xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway AT liudailin xuanfeibaiduformulaattenuateslpsinducedacutelunginjurybyinhibitingthenfkbsignalingpathway |