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Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism

Qishen granules (QSG), a traditional Chinese medicine, have been prescribed widely in the treatment of coronary heart diseases. Previous studies demonstrated that QSG had anti-inflammatory and cardio-protective effects in mice with acute myocardial infarction (AMI). However, the mechanisms by which...

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Autores principales: Li, Chun, Wang, Jing, Wang, Qiyan, Zhang, Yi, Zhang, Na, Lu, Linghui, Wu, Yan, Zhang, Qian, Wang, Wei, Wang, Yong, Tu, Pengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105076/
https://www.ncbi.nlm.nih.gov/pubmed/27833128
http://dx.doi.org/10.1038/srep36949
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author Li, Chun
Wang, Jing
Wang, Qiyan
Zhang, Yi
Zhang, Na
Lu, Linghui
Wu, Yan
Zhang, Qian
Wang, Wei
Wang, Yong
Tu, Pengfei
author_facet Li, Chun
Wang, Jing
Wang, Qiyan
Zhang, Yi
Zhang, Na
Lu, Linghui
Wu, Yan
Zhang, Qian
Wang, Wei
Wang, Yong
Tu, Pengfei
author_sort Li, Chun
collection PubMed
description Qishen granules (QSG), a traditional Chinese medicine, have been prescribed widely in the treatment of coronary heart diseases. Previous studies demonstrated that QSG had anti-inflammatory and cardio-protective effects in mice with acute myocardial infarction (AMI). However, the mechanisms by which QSG attenuate inflammation and prevent post-AMI heart failure (HF) are still unclear. In this study, we explored the anti-inflammatory mechanisms of QSG by in vitro and in vivo experiments. A novel inflammatory injury model of H9C2 cells was induced by lipopolysaccharide (LPS)-stimulated macrophage-conditioned media (CM). An animal model of AMI was conducted by ligation of left anterior descending (LAD) coronary artery in mice. We found that QSG inhibited release of cytokines from LPS-stimulated RAW 264.7 macrophages and protected H9C2 cardiac cells against CM-induced injury. In vivo results showed that QSG administration could improve cardiac functions and alter pathological changes in model of AMI. QSG regulated multiple key molecules, including phospholipases A2 (PLA2), cyclooxygenases (COXs) and lipoxygenases (LOXs), in arachidonic acid metabolism pathway. Interestingly, QSG also targeted TNF-α-NF-κB and IL-6-JAK2-STAT3 signaling pathways. Taken together, QSG achieve synergistic effects in mitigating post-AMI HF by regulating multiple targets in inflammatory pathways. This study provides insights into anti-inflammatory therapeutics in managing HF after AMI.
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spelling pubmed-51050762016-11-17 Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism Li, Chun Wang, Jing Wang, Qiyan Zhang, Yi Zhang, Na Lu, Linghui Wu, Yan Zhang, Qian Wang, Wei Wang, Yong Tu, Pengfei Sci Rep Article Qishen granules (QSG), a traditional Chinese medicine, have been prescribed widely in the treatment of coronary heart diseases. Previous studies demonstrated that QSG had anti-inflammatory and cardio-protective effects in mice with acute myocardial infarction (AMI). However, the mechanisms by which QSG attenuate inflammation and prevent post-AMI heart failure (HF) are still unclear. In this study, we explored the anti-inflammatory mechanisms of QSG by in vitro and in vivo experiments. A novel inflammatory injury model of H9C2 cells was induced by lipopolysaccharide (LPS)-stimulated macrophage-conditioned media (CM). An animal model of AMI was conducted by ligation of left anterior descending (LAD) coronary artery in mice. We found that QSG inhibited release of cytokines from LPS-stimulated RAW 264.7 macrophages and protected H9C2 cardiac cells against CM-induced injury. In vivo results showed that QSG administration could improve cardiac functions and alter pathological changes in model of AMI. QSG regulated multiple key molecules, including phospholipases A2 (PLA2), cyclooxygenases (COXs) and lipoxygenases (LOXs), in arachidonic acid metabolism pathway. Interestingly, QSG also targeted TNF-α-NF-κB and IL-6-JAK2-STAT3 signaling pathways. Taken together, QSG achieve synergistic effects in mitigating post-AMI HF by regulating multiple targets in inflammatory pathways. This study provides insights into anti-inflammatory therapeutics in managing HF after AMI. Nature Publishing Group 2016-11-11 /pmc/articles/PMC5105076/ /pubmed/27833128 http://dx.doi.org/10.1038/srep36949 Text en Copyright © 2016, 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
Li, Chun
Wang, Jing
Wang, Qiyan
Zhang, Yi
Zhang, Na
Lu, Linghui
Wu, Yan
Zhang, Qian
Wang, Wei
Wang, Yong
Tu, Pengfei
Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism
title Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism
title_full Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism
title_fullStr Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism
title_full_unstemmed Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism
title_short Qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism
title_sort qishen granules inhibit myocardial inflammation injury through regulating arachidonic acid metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105076/
https://www.ncbi.nlm.nih.gov/pubmed/27833128
http://dx.doi.org/10.1038/srep36949
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