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Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach

This study aimed to elucidate the mechanism of action of Runyan Mixture in treating pharyngitis using a network pharmacological approach. The active components of the Runyan Mixture were obtained from the traditional chinese medicine systems pharmacology database and evaluated using Lipinski’s rules...

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Autores principales: Zhang, Huihui, Tong, Yingpeng, Jin, Yinzhi, Cai, Guoyun, Li, Zhenxin, Pan, Xinling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794313/
https://www.ncbi.nlm.nih.gov/pubmed/36595833
http://dx.doi.org/10.1097/MD.0000000000032437
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author Zhang, Huihui
Tong, Yingpeng
Jin, Yinzhi
Cai, Guoyun
Li, Zhenxin
Pan, Xinling
author_facet Zhang, Huihui
Tong, Yingpeng
Jin, Yinzhi
Cai, Guoyun
Li, Zhenxin
Pan, Xinling
author_sort Zhang, Huihui
collection PubMed
description This study aimed to elucidate the mechanism of action of Runyan Mixture in treating pharyngitis using a network pharmacological approach. The active components of the Runyan Mixture were obtained from the traditional chinese medicine systems pharmacology database and evaluated using Lipinski’s rules. The SwissTargetPrediction database was used to predict the action targets of the Runyan Mixture, and a protein-protein interaction network was constructed using the STRING database. Moreover, the anti-inflammatory effect of Runyan Mixture was validated in vitro using the lipopolysaccharide induced inflammation in macrophages. The Runyan Mixture was the liquid preparation from 8 traditional Chinese medicine. A total of 89 types of active components, 53 core targets, and 98 signaling pathways (P < .001) were identified for the Runyan Mixture. The main action targets were EGFR, MAPK1, AKT1, PIK3CA, NFKB1, SRC, TNF, MAPK8, MET, and PTGS2. Among the identified signaling pathways, 20 were associated with microbial infection and 24 were related to the immune-inflammatory response. Experimental results in vitro showed that Runyan Mixture could significantly inhibit the expression of interleukin-1, interleukin-6, and tumor necrosis factor-α (P < .05) in macrophages by lipopolysaccharide stimulation. Based on the results of the protein-protein interaction network analysis and the anti-inflammatory effect in vitro, the efficiency of the Runyan Mixture in pharyngitis treatment could be attributed to the inhibition of the inflammatory response.
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spelling pubmed-97943132022-12-28 Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach Zhang, Huihui Tong, Yingpeng Jin, Yinzhi Cai, Guoyun Li, Zhenxin Pan, Xinling Medicine (Baltimore) 3800 This study aimed to elucidate the mechanism of action of Runyan Mixture in treating pharyngitis using a network pharmacological approach. The active components of the Runyan Mixture were obtained from the traditional chinese medicine systems pharmacology database and evaluated using Lipinski’s rules. The SwissTargetPrediction database was used to predict the action targets of the Runyan Mixture, and a protein-protein interaction network was constructed using the STRING database. Moreover, the anti-inflammatory effect of Runyan Mixture was validated in vitro using the lipopolysaccharide induced inflammation in macrophages. The Runyan Mixture was the liquid preparation from 8 traditional Chinese medicine. A total of 89 types of active components, 53 core targets, and 98 signaling pathways (P < .001) were identified for the Runyan Mixture. The main action targets were EGFR, MAPK1, AKT1, PIK3CA, NFKB1, SRC, TNF, MAPK8, MET, and PTGS2. Among the identified signaling pathways, 20 were associated with microbial infection and 24 were related to the immune-inflammatory response. Experimental results in vitro showed that Runyan Mixture could significantly inhibit the expression of interleukin-1, interleukin-6, and tumor necrosis factor-α (P < .05) in macrophages by lipopolysaccharide stimulation. Based on the results of the protein-protein interaction network analysis and the anti-inflammatory effect in vitro, the efficiency of the Runyan Mixture in pharyngitis treatment could be attributed to the inhibition of the inflammatory response. Lippincott Williams & Wilkins 2022-12-23 /pmc/articles/PMC9794313/ /pubmed/36595833 http://dx.doi.org/10.1097/MD.0000000000032437 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 3800
Zhang, Huihui
Tong, Yingpeng
Jin, Yinzhi
Cai, Guoyun
Li, Zhenxin
Pan, Xinling
Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach
title Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach
title_full Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach
title_fullStr Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach
title_full_unstemmed Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach
title_short Elucidation of the mechanism of action of Runyan Mixture in the treatment of pharyngitis using a network pharmacological approach
title_sort elucidation of the mechanism of action of runyan mixture in the treatment of pharyngitis using a network pharmacological approach
topic 3800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794313/
https://www.ncbi.nlm.nih.gov/pubmed/36595833
http://dx.doi.org/10.1097/MD.0000000000032437
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