Astragaloside IV enhances cardioprotection of remote ischemic conditioning after acute myocardial infarction in rats

被引:7
作者
Cheng, Songyi [1 ]
Yu, Peng [2 ]
Yang, Li [1 ]
Shi, Haibo [2 ]
He, Anxia [3 ]
Chen, Hanyu [1 ]
Han, Jie [1 ]
Xie, Liang [4 ]
Chen, Jiandong [2 ]
Chen, Xiaohu [2 ]
机构
[1] Nanjing Univ Chinese Med, Clin Med Coll 1, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Affiliated Hosp, Jiangsu Prov Hosp Tradit Chinese Med, Dept Cardiol, Hanzhong Rd 155, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Affiliated Hosp, Jiangsu Prov Hosp Tradit Chinese Med, Dept Ultrasonog, Nanjing 210029, Jiangsu, Peoples R China
[4] Nanjing Univ, Jinling Hosp, Dept Cardiol, Affiliated Hosp, Nanjing 210002, Jiangsu, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2016年 / 8卷 / 11期
基金
中国国家自然科学基金;
关键词
Astragaloside IV; remote ischemic conditioning; acute myocardial infarction; ventricular remodeling; cardioprotection; PERCUTANEOUS CORONARY INTERVENTION; CHRONIC HEART-FAILURE; DEPENDENT MECHANISM; INDUCED INJURY; REPERFUSION; CARDIOMYOCYTES; COMBINATION; EXPRESSION; REDUCTION; APOPTOSIS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Remote ischemic conditioning (RIC) has been shown to be a practical method for protecting the heart from ischemic/reperfusion (I/R) injury. In the present study, we investigated whether or not the combination of RIC and Astragaloside IV (AS-IV) could improve cardioprotection against acute myocardial infarction (AMI)induced heart failure (HF) when compared with individual treatments. Material and Methods: A rat model of AMI was established via permanent ligation of the left anterior descending coronary artery (LAD). Postoperatively, the rats were randomly grouped into a sham group (n=10), a model group (n=15), an AS-IV alone group (n=15), an RIC alone group (n=15) and a combined treatment group (AS-IV+RIC; n=15). All treatments were administered for 2 weeks. Results: After treatment for 2 weeks, the survival rate was improved, the cardiac function was preserved and the infarcted size was limited in AS-IV alone and RIC alone treatment groups compared to the model group, whereas the combined treatment yielded the most optimal protective effects. Additional studies suggested that AS-IV enhanced the cardioprotective effects of RIC by alleviating myocardial fibrosis, suppressing inflammation, attenuating apoptosis and ameliorating impairment of the myocardial ultrastructural. Conclusion: AS-IV enhances the cardioprotective effects of RIC against AMI-induced HF and ventricular remodeling, which represents a potential therapeutic approach for preserving cardiac function and improving the prognosis of AMI.
引用
收藏
页码:4657 / 4669
页数:13
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