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Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach
Herb pair Danggui-Honghua has been frequently used for treatment of blood stasis syndrome (BSS) in China, one of the most common clinical pathological syndromes in traditional Chinese medicine (TCM). However, its therapeutic mechanism has not been clearly elucidated. In the present study, a feasible...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225497/ https://www.ncbi.nlm.nih.gov/pubmed/28074863 http://dx.doi.org/10.1038/srep40318 |
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author | Yue, Shi-Jun Xin, Lan-Ting Fan, Ya-Chu Li, Shu-Jiao Tang, Yu-Ping Duan, Jin-Ao Guan, Hua-Shi Wang, Chang-Yun |
author_facet | Yue, Shi-Jun Xin, Lan-Ting Fan, Ya-Chu Li, Shu-Jiao Tang, Yu-Ping Duan, Jin-Ao Guan, Hua-Shi Wang, Chang-Yun |
author_sort | Yue, Shi-Jun |
collection | PubMed |
description | Herb pair Danggui-Honghua has been frequently used for treatment of blood stasis syndrome (BSS) in China, one of the most common clinical pathological syndromes in traditional Chinese medicine (TCM). However, its therapeutic mechanism has not been clearly elucidated. In the present study, a feasible system pharmacology model based on chemical, pharmacokinetic and pharmacological data was developed via network construction approach to clarify the mechanisms of this herb pair. Thirty-one active ingredients of Danggui-Honghua possessing favorable pharmacokinetic profiles and biological activities were selected, interacting with 42 BSS-related targets to provide potential synergistic therapeutic actions. Systematic analysis of the constructed networks revealed that these targets such as HMOX1, NOS2, NOS3, HIF1A and PTGS2 were mainly involved in TNF signaling pathway, HIF-1 signaling pathway, estrogen signaling pathway and neurotrophin signaling pathway. The contribution index of every active ingredient also indicated six compounds, including hydroxysafflor yellow A, safflor yellow A, safflor yellow B, Z-ligustilide, ferulic acid, and Z-butylidenephthalide, as the principal components of this herb pair. These results successfully explained the polypharmcological mechanisms underlying the efficiency of Danggui-Honghua for BSS treatment, and also probed into the potential novel therapeutic strategies for BSS in TCM. |
format | Online Article Text |
id | pubmed-5225497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52254972017-01-17 Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach Yue, Shi-Jun Xin, Lan-Ting Fan, Ya-Chu Li, Shu-Jiao Tang, Yu-Ping Duan, Jin-Ao Guan, Hua-Shi Wang, Chang-Yun Sci Rep Article Herb pair Danggui-Honghua has been frequently used for treatment of blood stasis syndrome (BSS) in China, one of the most common clinical pathological syndromes in traditional Chinese medicine (TCM). However, its therapeutic mechanism has not been clearly elucidated. In the present study, a feasible system pharmacology model based on chemical, pharmacokinetic and pharmacological data was developed via network construction approach to clarify the mechanisms of this herb pair. Thirty-one active ingredients of Danggui-Honghua possessing favorable pharmacokinetic profiles and biological activities were selected, interacting with 42 BSS-related targets to provide potential synergistic therapeutic actions. Systematic analysis of the constructed networks revealed that these targets such as HMOX1, NOS2, NOS3, HIF1A and PTGS2 were mainly involved in TNF signaling pathway, HIF-1 signaling pathway, estrogen signaling pathway and neurotrophin signaling pathway. The contribution index of every active ingredient also indicated six compounds, including hydroxysafflor yellow A, safflor yellow A, safflor yellow B, Z-ligustilide, ferulic acid, and Z-butylidenephthalide, as the principal components of this herb pair. These results successfully explained the polypharmcological mechanisms underlying the efficiency of Danggui-Honghua for BSS treatment, and also probed into the potential novel therapeutic strategies for BSS in TCM. Nature Publishing Group 2017-01-11 /pmc/articles/PMC5225497/ /pubmed/28074863 http://dx.doi.org/10.1038/srep40318 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yue, Shi-Jun Xin, Lan-Ting Fan, Ya-Chu Li, Shu-Jiao Tang, Yu-Ping Duan, Jin-Ao Guan, Hua-Shi Wang, Chang-Yun Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach |
title | Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach |
title_full | Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach |
title_fullStr | Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach |
title_full_unstemmed | Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach |
title_short | Herb pair Danggui-Honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach |
title_sort | herb pair danggui-honghua: mechanisms underlying blood stasis syndrome by system pharmacology approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225497/ https://www.ncbi.nlm.nih.gov/pubmed/28074863 http://dx.doi.org/10.1038/srep40318 |
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