Cargando…

Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice

Right ventricular (RV) dysfunction and failure contribute to the increasing morbidity and mortality of cardiovascular diseases; however, current treatment strategies are grossly inadequate. Sheng-Mai-San (SMS) has been used to treat heart diseases for hundreds of years in China, and its protective e...

Descripción completa

Detalles Bibliográficos
Autores principales: Chai, Cheng-Zhi, Mo, Wei-Lan, Zhuang, Xian-Fei, Kou, Jun-Ping, Yan, Yong-Qing, Yu, Bo-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814671/
https://www.ncbi.nlm.nih.gov/pubmed/27073402
http://dx.doi.org/10.1155/2016/4682786
_version_ 1782424454680281088
author Chai, Cheng-Zhi
Mo, Wei-Lan
Zhuang, Xian-Fei
Kou, Jun-Ping
Yan, Yong-Qing
Yu, Bo-Yang
author_facet Chai, Cheng-Zhi
Mo, Wei-Lan
Zhuang, Xian-Fei
Kou, Jun-Ping
Yan, Yong-Qing
Yu, Bo-Yang
author_sort Chai, Cheng-Zhi
collection PubMed
description Right ventricular (RV) dysfunction and failure contribute to the increasing morbidity and mortality of cardiovascular diseases; however, current treatment strategies are grossly inadequate. Sheng-Mai-San (SMS) has been used to treat heart diseases for hundreds of years in China, and its protective effects on RV have not been observed. The present study was to investigate the protective effects of SMS aqueous extract on RV dysfunction in chronic intermittent hypoxia (CIH) mice model. The results showed that CIH mice model presented RV dysfunction and maladaptive compensation after 28-day-CIH and SMS treatment significantly reversed these changes. Diastolic function of RV was restored and systolic dysfunction was attenuated, including elevation of RV stroke volume and fractional shortening, as well as pulmonary circulation. Structurally, SMS treatment inhibited RV dilation, cardiomyocytes vacuolization, ultrastructure abnormalities, and the expression of cleaved caspase-3. Of importance, SMS showed remarkable antioxidant activity by decreasing the levels of malondialdehyde (MDA) and 4-hydroxynonenal (4-HNE), increasing the levels of superoxide dismutase (SOD) and heme oxygenase-1 (HO-1), as well as inhibiting the overexpression of 3-NT in RV. Our results indicate that SMS preserve RV structure and function in CIH-exposed mice by involving regulation in both ROS and Reactive Nitrogen Species (RNS) production.
format Online
Article
Text
id pubmed-4814671
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-48146712016-04-12 Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice Chai, Cheng-Zhi Mo, Wei-Lan Zhuang, Xian-Fei Kou, Jun-Ping Yan, Yong-Qing Yu, Bo-Yang Evid Based Complement Alternat Med Research Article Right ventricular (RV) dysfunction and failure contribute to the increasing morbidity and mortality of cardiovascular diseases; however, current treatment strategies are grossly inadequate. Sheng-Mai-San (SMS) has been used to treat heart diseases for hundreds of years in China, and its protective effects on RV have not been observed. The present study was to investigate the protective effects of SMS aqueous extract on RV dysfunction in chronic intermittent hypoxia (CIH) mice model. The results showed that CIH mice model presented RV dysfunction and maladaptive compensation after 28-day-CIH and SMS treatment significantly reversed these changes. Diastolic function of RV was restored and systolic dysfunction was attenuated, including elevation of RV stroke volume and fractional shortening, as well as pulmonary circulation. Structurally, SMS treatment inhibited RV dilation, cardiomyocytes vacuolization, ultrastructure abnormalities, and the expression of cleaved caspase-3. Of importance, SMS showed remarkable antioxidant activity by decreasing the levels of malondialdehyde (MDA) and 4-hydroxynonenal (4-HNE), increasing the levels of superoxide dismutase (SOD) and heme oxygenase-1 (HO-1), as well as inhibiting the overexpression of 3-NT in RV. Our results indicate that SMS preserve RV structure and function in CIH-exposed mice by involving regulation in both ROS and Reactive Nitrogen Species (RNS) production. Hindawi Publishing Corporation 2016 2016-03-17 /pmc/articles/PMC4814671/ /pubmed/27073402 http://dx.doi.org/10.1155/2016/4682786 Text en Copyright © 2016 Cheng-Zhi Chai et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chai, Cheng-Zhi
Mo, Wei-Lan
Zhuang, Xian-Fei
Kou, Jun-Ping
Yan, Yong-Qing
Yu, Bo-Yang
Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice
title Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice
title_full Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice
title_fullStr Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice
title_full_unstemmed Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice
title_short Protective Effects of Sheng-Mai-San on Right Ventricular Dysfunction during Chronic Intermittent Hypoxia in Mice
title_sort protective effects of sheng-mai-san on right ventricular dysfunction during chronic intermittent hypoxia in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814671/
https://www.ncbi.nlm.nih.gov/pubmed/27073402
http://dx.doi.org/10.1155/2016/4682786
work_keys_str_mv AT chaichengzhi protectiveeffectsofshengmaisanonrightventriculardysfunctionduringchronicintermittenthypoxiainmice
AT moweilan protectiveeffectsofshengmaisanonrightventriculardysfunctionduringchronicintermittenthypoxiainmice
AT zhuangxianfei protectiveeffectsofshengmaisanonrightventriculardysfunctionduringchronicintermittenthypoxiainmice
AT koujunping protectiveeffectsofshengmaisanonrightventriculardysfunctionduringchronicintermittenthypoxiainmice
AT yanyongqing protectiveeffectsofshengmaisanonrightventriculardysfunctionduringchronicintermittenthypoxiainmice
AT yuboyang protectiveeffectsofshengmaisanonrightventriculardysfunctionduringchronicintermittenthypoxiainmice