Cargando…
Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis
Background. Apoptosis plays vital roles in the progression of doxorubicin-induced cardiomyopathy (DOX-CM). Endoplasmic reticulum stress (ER stress) could induce specific apoptosis by caspase-12 dependent pathway. Shengmai Injection (SMI), a famous Traditional Chinese Medicine, could alleviate the he...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369903/ https://www.ncbi.nlm.nih.gov/pubmed/25839043 http://dx.doi.org/10.1155/2015/952671 |
_version_ | 1782362810723860480 |
---|---|
author | Chen, Yu Tang, Yong Xiang, Yin Xie, Yu-Quan Huang, Xiao-Hong Zhang, Ya-Chen |
author_facet | Chen, Yu Tang, Yong Xiang, Yin Xie, Yu-Quan Huang, Xiao-Hong Zhang, Ya-Chen |
author_sort | Chen, Yu |
collection | PubMed |
description | Background. Apoptosis plays vital roles in the progression of doxorubicin-induced cardiomyopathy (DOX-CM). Endoplasmic reticulum stress (ER stress) could induce specific apoptosis by caspase-12 dependent pathway. Shengmai Injection (SMI), a famous Traditional Chinese Medicine, could alleviate the heart damage via inhibiting myocardial apoptosis. However, it is unknown whether SMI can alleviate ER stress and its specific apoptosis in the setting of DOX-CM. Objective. To explore the effects of SMI on heart function, myocardial ER stress, and apoptosis of DOX-CM rats. Methods. Rats with DOX-CM were treated by SMI. Heart function was assessed by echocardiography and brain natriuretic peptide. Myocardial apoptosis was detected by TUNEL assay. ER stress was assessed by detecting the expressions of GRP78 and caspase-12. Results. At the end of eight-week, compared to control, significant heart dysfunction happened in DOX group. The ratio of apoptotic cardiomyocytes and the expressions of GRP78 and caspase-12 increased significantly (P < 0.05). Compared to DOX group, the apoptotic ratio and the expressions of GRP78 and caspase-12 significantly decreased in DOX + SMI group (P < 0.05), accompanied with improved heart function. Conclusion. SMI could alleviate myocardial ER stress and caspase-12 dependent apoptosis, which subsequently helped to improve the heart function of rats with DOX-CM. |
format | Online Article Text |
id | pubmed-4369903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-43699032015-04-02 Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis Chen, Yu Tang, Yong Xiang, Yin Xie, Yu-Quan Huang, Xiao-Hong Zhang, Ya-Chen Biomed Res Int Research Article Background. Apoptosis plays vital roles in the progression of doxorubicin-induced cardiomyopathy (DOX-CM). Endoplasmic reticulum stress (ER stress) could induce specific apoptosis by caspase-12 dependent pathway. Shengmai Injection (SMI), a famous Traditional Chinese Medicine, could alleviate the heart damage via inhibiting myocardial apoptosis. However, it is unknown whether SMI can alleviate ER stress and its specific apoptosis in the setting of DOX-CM. Objective. To explore the effects of SMI on heart function, myocardial ER stress, and apoptosis of DOX-CM rats. Methods. Rats with DOX-CM were treated by SMI. Heart function was assessed by echocardiography and brain natriuretic peptide. Myocardial apoptosis was detected by TUNEL assay. ER stress was assessed by detecting the expressions of GRP78 and caspase-12. Results. At the end of eight-week, compared to control, significant heart dysfunction happened in DOX group. The ratio of apoptotic cardiomyocytes and the expressions of GRP78 and caspase-12 increased significantly (P < 0.05). Compared to DOX group, the apoptotic ratio and the expressions of GRP78 and caspase-12 significantly decreased in DOX + SMI group (P < 0.05), accompanied with improved heart function. Conclusion. SMI could alleviate myocardial ER stress and caspase-12 dependent apoptosis, which subsequently helped to improve the heart function of rats with DOX-CM. Hindawi Publishing Corporation 2015 2015-03-09 /pmc/articles/PMC4369903/ /pubmed/25839043 http://dx.doi.org/10.1155/2015/952671 Text en Copyright © 2015 Yu Chen et al. https://creativecommons.org/licenses/by/3.0/ 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 Chen, Yu Tang, Yong Xiang, Yin Xie, Yu-Quan Huang, Xiao-Hong Zhang, Ya-Chen Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis |
title | Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis |
title_full | Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis |
title_fullStr | Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis |
title_full_unstemmed | Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis |
title_short | Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis |
title_sort | shengmai injection improved doxorubicin-induced cardiomyopathy by alleviating myocardial endoplasmic reticulum stress and caspase-12 dependent apoptosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369903/ https://www.ncbi.nlm.nih.gov/pubmed/25839043 http://dx.doi.org/10.1155/2015/952671 |
work_keys_str_mv | AT chenyu shengmaiinjectionimproveddoxorubicininducedcardiomyopathybyalleviatingmyocardialendoplasmicreticulumstressandcaspase12dependentapoptosis AT tangyong shengmaiinjectionimproveddoxorubicininducedcardiomyopathybyalleviatingmyocardialendoplasmicreticulumstressandcaspase12dependentapoptosis AT xiangyin shengmaiinjectionimproveddoxorubicininducedcardiomyopathybyalleviatingmyocardialendoplasmicreticulumstressandcaspase12dependentapoptosis AT xieyuquan shengmaiinjectionimproveddoxorubicininducedcardiomyopathybyalleviatingmyocardialendoplasmicreticulumstressandcaspase12dependentapoptosis AT huangxiaohong shengmaiinjectionimproveddoxorubicininducedcardiomyopathybyalleviatingmyocardialendoplasmicreticulumstressandcaspase12dependentapoptosis AT zhangyachen shengmaiinjectionimproveddoxorubicininducedcardiomyopathybyalleviatingmyocardialendoplasmicreticulumstressandcaspase12dependentapoptosis |