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Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats
BACKGROUND: Danshen-Gegen decoction (DG), a Chinese herbal formula, has been demonstrated to be effective for the treatment of coronary heart disease such as myocardial infarction. In the present study, we investigated the effect of DG post-conditioning on isoproterenol (ISO)-induced myocardial inju...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055215/ https://www.ncbi.nlm.nih.gov/pubmed/21320349 http://dx.doi.org/10.1186/1749-8546-6-7 |
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author | Wong, Sze Man Chiu, Po Yee Leung, Hoi Yan Zhou, Limin Zuo, Zhong Lam, Philip Y Ko, Kam Ming |
author_facet | Wong, Sze Man Chiu, Po Yee Leung, Hoi Yan Zhou, Limin Zuo, Zhong Lam, Philip Y Ko, Kam Ming |
author_sort | Wong, Sze Man |
collection | PubMed |
description | BACKGROUND: Danshen-Gegen decoction (DG), a Chinese herbal formula, has been demonstrated to be effective for the treatment of coronary heart disease such as myocardial infarction. In the present study, we investigated the effect of DG post-conditioning on isoproterenol (ISO)-induced myocardial injury in rats. METHODS: ISO was injected intraperitoneally (200 mg/kg) to induce acute (2-6 hours) myocardial injury in adult female rats. DG (4 g/kg) was administered per oral immediately after the injection of ISO in the rats. Extent of myocardial injury was assessed by measurements of plasma enzyme activities. Myocardial mitochondrial glutathione antioxidant status, lipid peroxidation and mitochondrial calcium ion loading and cytochrome c release were also measured. Effects of inhibitors of protein kinase C-epsilon (PKCε) ranslocation and mitochondrial ATP-sensitive potassium channel (mK(ATP)) on myocardial post-conditioning by DG were investigated. RESULTS: ISO inflicted acute myocardial injury in the rats as evidenced by increased plasma enzyme activities. DG post-treatment alleviated the ISO-induced acute myocardial injury. CONCLUSION: DG post-treatment protected the myocardium against ISO-induced acute injury in rats. The myocardial post-conditioning by DG is likely mediated by PKCε/mK(ATP )signaling pathway. |
format | Text |
id | pubmed-3055215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30552152011-03-12 Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats Wong, Sze Man Chiu, Po Yee Leung, Hoi Yan Zhou, Limin Zuo, Zhong Lam, Philip Y Ko, Kam Ming Chin Med Research BACKGROUND: Danshen-Gegen decoction (DG), a Chinese herbal formula, has been demonstrated to be effective for the treatment of coronary heart disease such as myocardial infarction. In the present study, we investigated the effect of DG post-conditioning on isoproterenol (ISO)-induced myocardial injury in rats. METHODS: ISO was injected intraperitoneally (200 mg/kg) to induce acute (2-6 hours) myocardial injury in adult female rats. DG (4 g/kg) was administered per oral immediately after the injection of ISO in the rats. Extent of myocardial injury was assessed by measurements of plasma enzyme activities. Myocardial mitochondrial glutathione antioxidant status, lipid peroxidation and mitochondrial calcium ion loading and cytochrome c release were also measured. Effects of inhibitors of protein kinase C-epsilon (PKCε) ranslocation and mitochondrial ATP-sensitive potassium channel (mK(ATP)) on myocardial post-conditioning by DG were investigated. RESULTS: ISO inflicted acute myocardial injury in the rats as evidenced by increased plasma enzyme activities. DG post-treatment alleviated the ISO-induced acute myocardial injury. CONCLUSION: DG post-treatment protected the myocardium against ISO-induced acute injury in rats. The myocardial post-conditioning by DG is likely mediated by PKCε/mK(ATP )signaling pathway. BioMed Central 2011-02-14 /pmc/articles/PMC3055215/ /pubmed/21320349 http://dx.doi.org/10.1186/1749-8546-6-7 Text en Copyright ©2011 Wong et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wong, Sze Man Chiu, Po Yee Leung, Hoi Yan Zhou, Limin Zuo, Zhong Lam, Philip Y Ko, Kam Ming Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats |
title | Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats |
title_full | Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats |
title_fullStr | Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats |
title_full_unstemmed | Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats |
title_short | Myocardial post-conditioning with Danshen-Gegen decoction protects against isoproterenol-induced myocardial injury via a PKCε/mK(ATP)-mediated pathway in rats |
title_sort | myocardial post-conditioning with danshen-gegen decoction protects against isoproterenol-induced myocardial injury via a pkcε/mk(atp)-mediated pathway in rats |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055215/ https://www.ncbi.nlm.nih.gov/pubmed/21320349 http://dx.doi.org/10.1186/1749-8546-6-7 |
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