Cargando…
PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R
The prevention and management of myocardial ischemia/reperfusion (MI/R) injury is an essential part of coronary heart disease surgery and is becoming a major clinical problem in the treatment of ischemic heart disease. Previous studies by our group have demonstrated that pigment epithelium-derived f...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881792/ https://www.ncbi.nlm.nih.gov/pubmed/29532859 http://dx.doi.org/10.3892/ijmm.2018.3552 |
_version_ | 1783311368055685120 |
---|---|
author | Zhao, Qixiang Liu, Zhiwei Huang, Bing Yuan, Yanliang Liu, Xiucheng Zhang, Hu Qiu, Fan Zhang, Yiqian Li, Yufeng Miao, Haoran Dong, Hongyan Zhang, Zhongming |
author_facet | Zhao, Qixiang Liu, Zhiwei Huang, Bing Yuan, Yanliang Liu, Xiucheng Zhang, Hu Qiu, Fan Zhang, Yiqian Li, Yufeng Miao, Haoran Dong, Hongyan Zhang, Zhongming |
author_sort | Zhao, Qixiang |
collection | PubMed |
description | The prevention and management of myocardial ischemia/reperfusion (MI/R) injury is an essential part of coronary heart disease surgery and is becoming a major clinical problem in the treatment of ischemic heart disease. Previous studies by our group have demonstrated that pigment epithelium-derived factor (PEDF) improves cardiac function in rats with acute myocardial infarction and reduces hypoxia-induced cell injury. However, the protective function and mechanisms underlying the effect of PEDF in MI/R injury remain to be fully understood. In the present study, the positive effect of PEDF in MI/R injury was confirmed by construction of the adult Sprague-Dawley rat MI/R model. PEDF reduced myocardial infarct size and downregulated cardiomyocyte apoptosis in the I/R myocardium in this model. In addition, PEDF improved cardiac function and increased cardiac functional reserve in rats subjected to MI/R Injury. To further study the protective effect of PEDF and the underlying mechanisms in MI/R injury, a H9c2 cardiomyocyte hypoxia/reoxygenation (H/R) model was constructed. PEDF was confirmed to decrease H/R-induced apoptosis in H9c2 cells, and this anti-apoptotic function was abolished by pigment epithelium-derived factor-receptor (PEDF R) small interfering (si)RNA. Furthermore, administration of PEDF decreased the levels of reactive oxygen species (ROS) and malondialdehyde (MDA) in H/R H9c2 cells. Compared with the H/R group, PEDF decreased mitochondrial ROS, increased the mitochondrial DNA copy number, reduced xanthine oxidase and NADPH oxidase activity, as well as RAC family small GTPase 1 protein expression. However, these effects of PEDF were markedly attenuated by PEDF-R siRNA. To the best of our knowledge, the present study is the first to identify the protective effect of PEDF in MI/R injury, and confirm that the antioxidative effect PEDF occurred via inhibition of ROS generation via PEDF-R under MI/R conditions. |
format | Online Article Text |
id | pubmed-5881792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-58817922018-04-12 PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R Zhao, Qixiang Liu, Zhiwei Huang, Bing Yuan, Yanliang Liu, Xiucheng Zhang, Hu Qiu, Fan Zhang, Yiqian Li, Yufeng Miao, Haoran Dong, Hongyan Zhang, Zhongming Int J Mol Med Articles The prevention and management of myocardial ischemia/reperfusion (MI/R) injury is an essential part of coronary heart disease surgery and is becoming a major clinical problem in the treatment of ischemic heart disease. Previous studies by our group have demonstrated that pigment epithelium-derived factor (PEDF) improves cardiac function in rats with acute myocardial infarction and reduces hypoxia-induced cell injury. However, the protective function and mechanisms underlying the effect of PEDF in MI/R injury remain to be fully understood. In the present study, the positive effect of PEDF in MI/R injury was confirmed by construction of the adult Sprague-Dawley rat MI/R model. PEDF reduced myocardial infarct size and downregulated cardiomyocyte apoptosis in the I/R myocardium in this model. In addition, PEDF improved cardiac function and increased cardiac functional reserve in rats subjected to MI/R Injury. To further study the protective effect of PEDF and the underlying mechanisms in MI/R injury, a H9c2 cardiomyocyte hypoxia/reoxygenation (H/R) model was constructed. PEDF was confirmed to decrease H/R-induced apoptosis in H9c2 cells, and this anti-apoptotic function was abolished by pigment epithelium-derived factor-receptor (PEDF R) small interfering (si)RNA. Furthermore, administration of PEDF decreased the levels of reactive oxygen species (ROS) and malondialdehyde (MDA) in H/R H9c2 cells. Compared with the H/R group, PEDF decreased mitochondrial ROS, increased the mitochondrial DNA copy number, reduced xanthine oxidase and NADPH oxidase activity, as well as RAC family small GTPase 1 protein expression. However, these effects of PEDF were markedly attenuated by PEDF-R siRNA. To the best of our knowledge, the present study is the first to identify the protective effect of PEDF in MI/R injury, and confirm that the antioxidative effect PEDF occurred via inhibition of ROS generation via PEDF-R under MI/R conditions. D.A. Spandidos 2018-06 2018-03-09 /pmc/articles/PMC5881792/ /pubmed/29532859 http://dx.doi.org/10.3892/ijmm.2018.3552 Text en Copyright: © Zhao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhao, Qixiang Liu, Zhiwei Huang, Bing Yuan, Yanliang Liu, Xiucheng Zhang, Hu Qiu, Fan Zhang, Yiqian Li, Yufeng Miao, Haoran Dong, Hongyan Zhang, Zhongming PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R |
title | PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R |
title_full | PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R |
title_fullStr | PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R |
title_full_unstemmed | PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R |
title_short | PEDF improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ROS generation via PEDF-R |
title_sort | pedf improves cardiac function in rats subjected to myocardial ischemia/reperfusion injury by inhibiting ros generation via pedf-r |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881792/ https://www.ncbi.nlm.nih.gov/pubmed/29532859 http://dx.doi.org/10.3892/ijmm.2018.3552 |
work_keys_str_mv | AT zhaoqixiang pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT liuzhiwei pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT huangbing pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT yuanyanliang pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT liuxiucheng pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT zhanghu pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT qiufan pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT zhangyiqian pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT liyufeng pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT miaohaoran pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT donghongyan pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr AT zhangzhongming pedfimprovescardiacfunctioninratssubjectedtomyocardialischemiareperfusioninjurybyinhibitingrosgenerationviapedfr |