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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-5105076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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