Cargando…

Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats

BACKGROUND: Our previous studies suggested that deoxyschizandrin (DSD) and schisantherin A (STA) may have cardioprotective effects, but information in this regard is lacking. Therefore, we explored the protective role of DSD and STA in myocardial ischemia–reperfusion (I/R) injury. METHODOLOGY/PRINCI...

Descripción completa

Detalles Bibliográficos
Autores principales: Chang, Ruimiao, Li, Yong, Yang, Xingxin, Yue, Yuan, Dou, Lili, Wang, Yanwei, Zhang, Weifang, Li, Xiaoni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631228/
https://www.ncbi.nlm.nih.gov/pubmed/23620773
http://dx.doi.org/10.1371/journal.pone.0061590
_version_ 1782266771585105920
author Chang, Ruimiao
Li, Yong
Yang, Xingxin
Yue, Yuan
Dou, Lili
Wang, Yanwei
Zhang, Weifang
Li, Xiaoni
author_facet Chang, Ruimiao
Li, Yong
Yang, Xingxin
Yue, Yuan
Dou, Lili
Wang, Yanwei
Zhang, Weifang
Li, Xiaoni
author_sort Chang, Ruimiao
collection PubMed
description BACKGROUND: Our previous studies suggested that deoxyschizandrin (DSD) and schisantherin A (STA) may have cardioprotective effects, but information in this regard is lacking. Therefore, we explored the protective role of DSD and STA in myocardial ischemia–reperfusion (I/R) injury. METHODOLOGY/PRINCIPAL FINDINGS: Anesthetized male rats were treated once with DSD and STA (each 40 µmol/kg) through the tail vein after 45 min of ischemia, followed by 2-h reperfusion. Cardiac function, infarct size, biochemical markers, histopathology and apoptosis were measured and mRNA expression of gp91(phox) in myocardial tissue assessed by RT-PCR. Neonatal rat cardiomyocytes were pretreated with DSD and STA and then damaged by H(2)O(2). Cell apoptosis was tested by a flow cytometric assay. Compared with the I/R group: (i) DSD and STA could significantly reduce the abnormalities of LVSP, LVEDP, ±dp/dt(max) and arrhythmias, thereby showing their protective roles in cardiac function; (ii) DSD and STA could significantly attenuate the infarct size and MDA release while increasing SOD activity, suggesting a role in reducing myocardial injury; (iii) tissue morphology and myocardial textual analysis revealed that DSD and STA mitigated changes in myocardial histopathology; (iv) DSD and STA decreased apoptosis (33.56±2.58% to 10.28±2.80% and 10.98±1.99%, respectively) and caspase-3 activity in the myocardium (0.62±0.02 OD/mg to 0.38±0.02 OD/mg and 0.32±0.02 OD/mg, respectively), showing their protective effects upon cardiomyocytes; and (v) DSD and STA had similar protective effects on I/R injury as those seen with the positive control metoprolol. In vitro, DSD and STA could significantly decrease the apoptosis of neonatal cardiomyocytes. CONCLUSIONS/SIGNIFICANCE: These data suggest that DSD and STA can protect against myocardial I/R injury. The underlining mechanism may be related to their role in inhibiting cardiomyocyte apoptosis.
format Online
Article
Text
id pubmed-3631228
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36312282013-04-25 Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats Chang, Ruimiao Li, Yong Yang, Xingxin Yue, Yuan Dou, Lili Wang, Yanwei Zhang, Weifang Li, Xiaoni PLoS One Research Article BACKGROUND: Our previous studies suggested that deoxyschizandrin (DSD) and schisantherin A (STA) may have cardioprotective effects, but information in this regard is lacking. Therefore, we explored the protective role of DSD and STA in myocardial ischemia–reperfusion (I/R) injury. METHODOLOGY/PRINCIPAL FINDINGS: Anesthetized male rats were treated once with DSD and STA (each 40 µmol/kg) through the tail vein after 45 min of ischemia, followed by 2-h reperfusion. Cardiac function, infarct size, biochemical markers, histopathology and apoptosis were measured and mRNA expression of gp91(phox) in myocardial tissue assessed by RT-PCR. Neonatal rat cardiomyocytes were pretreated with DSD and STA and then damaged by H(2)O(2). Cell apoptosis was tested by a flow cytometric assay. Compared with the I/R group: (i) DSD and STA could significantly reduce the abnormalities of LVSP, LVEDP, ±dp/dt(max) and arrhythmias, thereby showing their protective roles in cardiac function; (ii) DSD and STA could significantly attenuate the infarct size and MDA release while increasing SOD activity, suggesting a role in reducing myocardial injury; (iii) tissue morphology and myocardial textual analysis revealed that DSD and STA mitigated changes in myocardial histopathology; (iv) DSD and STA decreased apoptosis (33.56±2.58% to 10.28±2.80% and 10.98±1.99%, respectively) and caspase-3 activity in the myocardium (0.62±0.02 OD/mg to 0.38±0.02 OD/mg and 0.32±0.02 OD/mg, respectively), showing their protective effects upon cardiomyocytes; and (v) DSD and STA had similar protective effects on I/R injury as those seen with the positive control metoprolol. In vitro, DSD and STA could significantly decrease the apoptosis of neonatal cardiomyocytes. CONCLUSIONS/SIGNIFICANCE: These data suggest that DSD and STA can protect against myocardial I/R injury. The underlining mechanism may be related to their role in inhibiting cardiomyocyte apoptosis. Public Library of Science 2013-04-19 /pmc/articles/PMC3631228/ /pubmed/23620773 http://dx.doi.org/10.1371/journal.pone.0061590 Text en © 2013 Chang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chang, Ruimiao
Li, Yong
Yang, Xingxin
Yue, Yuan
Dou, Lili
Wang, Yanwei
Zhang, Weifang
Li, Xiaoni
Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats
title Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats
title_full Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats
title_fullStr Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats
title_full_unstemmed Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats
title_short Protective Role of Deoxyschizandrin and Schisantherin A against Myocardial Ischemia–Reperfusion Injury in Rats
title_sort protective role of deoxyschizandrin and schisantherin a against myocardial ischemia–reperfusion injury in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631228/
https://www.ncbi.nlm.nih.gov/pubmed/23620773
http://dx.doi.org/10.1371/journal.pone.0061590
work_keys_str_mv AT changruimiao protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats
AT liyong protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats
AT yangxingxin protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats
AT yueyuan protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats
AT doulili protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats
AT wangyanwei protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats
AT zhangweifang protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats
AT lixiaoni protectiveroleofdeoxyschizandrinandschisantherinaagainstmyocardialischemiareperfusioninjuryinrats