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Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro

Traditional Chinese medicine uses a systemic treatment approach, targeting multiple etiological factors simultaneously. Danhong injection (DHI), a very popular Chinese medicine injection, is reported to be effective for many cardiovascular conditions. The primary active ingredients of DHI, and their...

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Autores principales: Guan, Yue, Yin, Ying, Zhu, Yan-Rong, Guo, Chao, Wei, Guo, Duan, Jia-Lin, Wang, Yan-Hua, Zhou, Dan, Quan, Wei, Weng, Yan, Xi, Miao-Miao, Wen, Ai-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3686077/
https://www.ncbi.nlm.nih.gov/pubmed/23840272
http://dx.doi.org/10.1155/2013/972370
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author Guan, Yue
Yin, Ying
Zhu, Yan-Rong
Guo, Chao
Wei, Guo
Duan, Jia-Lin
Wang, Yan-Hua
Zhou, Dan
Quan, Wei
Weng, Yan
Xi, Miao-Miao
Wen, Ai-Dong
author_facet Guan, Yue
Yin, Ying
Zhu, Yan-Rong
Guo, Chao
Wei, Guo
Duan, Jia-Lin
Wang, Yan-Hua
Zhou, Dan
Quan, Wei
Weng, Yan
Xi, Miao-Miao
Wen, Ai-Dong
author_sort Guan, Yue
collection PubMed
description Traditional Chinese medicine uses a systemic treatment approach, targeting multiple etiological factors simultaneously. Danhong injection (DHI), a very popular Chinese medicine injection, is reported to be effective for many cardiovascular conditions. The primary active ingredients of DHI, and their systemic and interrelated mechanism have not been evaluated in an established myocardial ischemia/reperfusion (MI/R) model. We identified the main active constituents in DHI, including hydroxysafflor yellow A (A), salvianolic acid B (B), and danshensu (C), by HPLC fingerprint analysis and assessed their effect on MI/R rats and cardiomyocytes. These 3 compounds and DHI all decreased the levels of IL-1, TNF-α, and MDA, increased those of IL-10 and SOD activity in vivo and in vitro, and had antiapoptotic effects, as shown by flow cytometric analysis and TUNEL assay. Moreover, these compounds increased phosphorylation of Akt and ERK1/2 in cardiomyocytes. Interestingly, we found compound A exerted a more prominent anti-inflammatory effect than B and C, by decreasing NF-κB levels; compound B had more powerful antioxidative capacity than A and C, by increasing Nrf2 expression; compound C had stronger antiapoptotic ability than A and B, by lowering caspase-3 activity. Our results elucidate the mechanisms by which DHI protects against MI/R induced injury.
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spelling pubmed-36860772013-07-09 Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro Guan, Yue Yin, Ying Zhu, Yan-Rong Guo, Chao Wei, Guo Duan, Jia-Lin Wang, Yan-Hua Zhou, Dan Quan, Wei Weng, Yan Xi, Miao-Miao Wen, Ai-Dong Evid Based Complement Alternat Med Research Article Traditional Chinese medicine uses a systemic treatment approach, targeting multiple etiological factors simultaneously. Danhong injection (DHI), a very popular Chinese medicine injection, is reported to be effective for many cardiovascular conditions. The primary active ingredients of DHI, and their systemic and interrelated mechanism have not been evaluated in an established myocardial ischemia/reperfusion (MI/R) model. We identified the main active constituents in DHI, including hydroxysafflor yellow A (A), salvianolic acid B (B), and danshensu (C), by HPLC fingerprint analysis and assessed their effect on MI/R rats and cardiomyocytes. These 3 compounds and DHI all decreased the levels of IL-1, TNF-α, and MDA, increased those of IL-10 and SOD activity in vivo and in vitro, and had antiapoptotic effects, as shown by flow cytometric analysis and TUNEL assay. Moreover, these compounds increased phosphorylation of Akt and ERK1/2 in cardiomyocytes. Interestingly, we found compound A exerted a more prominent anti-inflammatory effect than B and C, by decreasing NF-κB levels; compound B had more powerful antioxidative capacity than A and C, by increasing Nrf2 expression; compound C had stronger antiapoptotic ability than A and B, by lowering caspase-3 activity. Our results elucidate the mechanisms by which DHI protects against MI/R induced injury. Hindawi Publishing Corporation 2013 2013-06-03 /pmc/articles/PMC3686077/ /pubmed/23840272 http://dx.doi.org/10.1155/2013/972370 Text en Copyright © 2013 Yue Guan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Guan, Yue
Yin, Ying
Zhu, Yan-Rong
Guo, Chao
Wei, Guo
Duan, Jia-Lin
Wang, Yan-Hua
Zhou, Dan
Quan, Wei
Weng, Yan
Xi, Miao-Miao
Wen, Ai-Dong
Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro
title Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro
title_full Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro
title_fullStr Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro
title_full_unstemmed Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro
title_short Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro
title_sort dissection of mechanisms of a chinese medicinal formula: danhong injection therapy for myocardial ischemia/reperfusion injury in vivo and in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3686077/
https://www.ncbi.nlm.nih.gov/pubmed/23840272
http://dx.doi.org/10.1155/2013/972370
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