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The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction

INTRODUCTION: After COVID-19, there was an outbreak of a new infectious disease caused by monkeypox virus. So far, no specific drug has been found to treat it. Xuanbai Chengqi decoction (XBCQD) has shown effects against a variety of viruses in China. METHODS: We searched for the active compounds and...

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Autores principales: Jiao, Yanqi, Shi, Chengcheng, Sun, Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553791/
https://www.ncbi.nlm.nih.gov/pubmed/37808322
http://dx.doi.org/10.3389/fmicb.2023.1234817
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author Jiao, Yanqi
Shi, Chengcheng
Sun, Yao
author_facet Jiao, Yanqi
Shi, Chengcheng
Sun, Yao
author_sort Jiao, Yanqi
collection PubMed
description INTRODUCTION: After COVID-19, there was an outbreak of a new infectious disease caused by monkeypox virus. So far, no specific drug has been found to treat it. Xuanbai Chengqi decoction (XBCQD) has shown effects against a variety of viruses in China. METHODS: We searched for the active compounds and potential targets for XBCQD from multiple open databases and literature. Monkeypox related targets were searched out from the OMIM and GeneCards databases. After determining the assumed targets of XBCQD for monkeypox treatment, we built the PPI network and used R for GO enrichment and KEGG pathway analysis. The interactions between the active compounds and the hub targets were investigated by molecular docking and molecular dynamics (MD) simulations. RESULTS: In total, 5 active compounds and 10 hub targets of XBCQD were screened out. GO enrichment and KEGG analysis demonstrated that XBCQD plays a therapeutic role in monkeypox mainly by regulating signaling pathways related to viral infection and inflammatory response. The main active compound estrone binding to target AR was confirmed to be the best therapy choice for monkeypox. DISCUSSION: This study systematically explored the interactions between the bioactive compounds of XBCQD and the monkeypox-specific XBCQD targets using network pharmacological methods, bioinformatics analyses and molecular simulations, suggesting that XBCQD could have a beneficial therapeutic effect on monkeypox by reducing the inflammatory damage and viral replication via multiple pathways. The use of XBCQD on monkeypox disease was confirmed to be best worked through the estrone-target AR interaction. Our work could provide evidence and guidance for further research on the treatment of monkeypox disease.
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spelling pubmed-105537912023-10-06 The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction Jiao, Yanqi Shi, Chengcheng Sun, Yao Front Microbiol Microbiology INTRODUCTION: After COVID-19, there was an outbreak of a new infectious disease caused by monkeypox virus. So far, no specific drug has been found to treat it. Xuanbai Chengqi decoction (XBCQD) has shown effects against a variety of viruses in China. METHODS: We searched for the active compounds and potential targets for XBCQD from multiple open databases and literature. Monkeypox related targets were searched out from the OMIM and GeneCards databases. After determining the assumed targets of XBCQD for monkeypox treatment, we built the PPI network and used R for GO enrichment and KEGG pathway analysis. The interactions between the active compounds and the hub targets were investigated by molecular docking and molecular dynamics (MD) simulations. RESULTS: In total, 5 active compounds and 10 hub targets of XBCQD were screened out. GO enrichment and KEGG analysis demonstrated that XBCQD plays a therapeutic role in monkeypox mainly by regulating signaling pathways related to viral infection and inflammatory response. The main active compound estrone binding to target AR was confirmed to be the best therapy choice for monkeypox. DISCUSSION: This study systematically explored the interactions between the bioactive compounds of XBCQD and the monkeypox-specific XBCQD targets using network pharmacological methods, bioinformatics analyses and molecular simulations, suggesting that XBCQD could have a beneficial therapeutic effect on monkeypox by reducing the inflammatory damage and viral replication via multiple pathways. The use of XBCQD on monkeypox disease was confirmed to be best worked through the estrone-target AR interaction. Our work could provide evidence and guidance for further research on the treatment of monkeypox disease. Frontiers Media S.A. 2023-09-20 /pmc/articles/PMC10553791/ /pubmed/37808322 http://dx.doi.org/10.3389/fmicb.2023.1234817 Text en Copyright © 2023 Jiao, Shi and Sun. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jiao, Yanqi
Shi, Chengcheng
Sun, Yao
The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction
title The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction
title_full The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction
title_fullStr The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction
title_full_unstemmed The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction
title_short The use of Xuanbai Chengqi decoction on monkeypox disease through the estrone-target AR interaction
title_sort use of xuanbai chengqi decoction on monkeypox disease through the estrone-target ar interaction
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553791/
https://www.ncbi.nlm.nih.gov/pubmed/37808322
http://dx.doi.org/10.3389/fmicb.2023.1234817
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