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Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective
Diesun Miaofang (DSMF) is a traditional herbal formula, which has been reported to activate blood, remove stasis, promote qi circulation and relieve pain. DSMF holds a great promise for the treatment of traumatic injury in an integrative and holistic manner. However, its underlying mechanisms remain...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464322/ https://www.ncbi.nlm.nih.gov/pubmed/25891262 http://dx.doi.org/10.3892/mmr.2015.3638 |
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author | ZHENG, CHUN-SONG FU, CHANG-LONG PAN, CAI-BIN BAO, HONG-JUAN CHEN, XING-QIANG YE, HONG-ZHI YE, JIN-XIA WU, GUANG-WEN LI, XI-HAI XU, HUI-FENG XU, XIAO-JIE LIU, XIAN-XIANG |
author_facet | ZHENG, CHUN-SONG FU, CHANG-LONG PAN, CAI-BIN BAO, HONG-JUAN CHEN, XING-QIANG YE, HONG-ZHI YE, JIN-XIA WU, GUANG-WEN LI, XI-HAI XU, HUI-FENG XU, XIAO-JIE LIU, XIAN-XIANG |
author_sort | ZHENG, CHUN-SONG |
collection | PubMed |
description | Diesun Miaofang (DSMF) is a traditional herbal formula, which has been reported to activate blood, remove stasis, promote qi circulation and relieve pain. DSMF holds a great promise for the treatment of traumatic injury in an integrative and holistic manner. However, its underlying mechanisms remain to be elucidated. In the present study, a systems pharmacology model, which integrated cluster ligands, human intestinal absorption and aqueous solution prediction, chemical space mapping, molecular docking and network pharmacology techniques were used. The compounds from DSMF were diverse in the clusters and chemical space. The majority of the compounds exhibited drug-like properties. A total of 59 compounds were identified to interact with 16 potential targets. In the herb-compound-target network, the majority of compounds acted on only one target; however, a small number of compounds acted on a large number of targets, up to a maximum of 12. The comparison of key topological properties in compound-target networks associated with the above efficacy intuitively demonstrated that potential active compounds possessed diverse functions. These results successfully explained the polypharmcological mechanism underlying the efficiency of DSMF for the treatment of traumatic injury as well as provided insight into potential novel therapeutic strategies for traumatic injury from herbal medicine. |
format | Online Article Text |
id | pubmed-4464322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-44643222015-06-26 Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective ZHENG, CHUN-SONG FU, CHANG-LONG PAN, CAI-BIN BAO, HONG-JUAN CHEN, XING-QIANG YE, HONG-ZHI YE, JIN-XIA WU, GUANG-WEN LI, XI-HAI XU, HUI-FENG XU, XIAO-JIE LIU, XIAN-XIANG Mol Med Rep Articles Diesun Miaofang (DSMF) is a traditional herbal formula, which has been reported to activate blood, remove stasis, promote qi circulation and relieve pain. DSMF holds a great promise for the treatment of traumatic injury in an integrative and holistic manner. However, its underlying mechanisms remain to be elucidated. In the present study, a systems pharmacology model, which integrated cluster ligands, human intestinal absorption and aqueous solution prediction, chemical space mapping, molecular docking and network pharmacology techniques were used. The compounds from DSMF were diverse in the clusters and chemical space. The majority of the compounds exhibited drug-like properties. A total of 59 compounds were identified to interact with 16 potential targets. In the herb-compound-target network, the majority of compounds acted on only one target; however, a small number of compounds acted on a large number of targets, up to a maximum of 12. The comparison of key topological properties in compound-target networks associated with the above efficacy intuitively demonstrated that potential active compounds possessed diverse functions. These results successfully explained the polypharmcological mechanism underlying the efficiency of DSMF for the treatment of traumatic injury as well as provided insight into potential novel therapeutic strategies for traumatic injury from herbal medicine. D.A. Spandidos 2015-08 2015-04-16 /pmc/articles/PMC4464322/ /pubmed/25891262 http://dx.doi.org/10.3892/mmr.2015.3638 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles ZHENG, CHUN-SONG FU, CHANG-LONG PAN, CAI-BIN BAO, HONG-JUAN CHEN, XING-QIANG YE, HONG-ZHI YE, JIN-XIA WU, GUANG-WEN LI, XI-HAI XU, HUI-FENG XU, XIAO-JIE LIU, XIAN-XIANG Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective |
title | Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective |
title_full | Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective |
title_fullStr | Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective |
title_full_unstemmed | Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective |
title_short | Deciphering the underlying mechanisms of Diesun Miaofang in traumatic injury from a systems pharmacology perspective |
title_sort | deciphering the underlying mechanisms of diesun miaofang in traumatic injury from a systems pharmacology perspective |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464322/ https://www.ncbi.nlm.nih.gov/pubmed/25891262 http://dx.doi.org/10.3892/mmr.2015.3638 |
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