Salvianolic Acid A Demonstrates Cardioprotective Effects in Rat Hearts and Cardiomyocytes After Ischemia/Reperfusion Injury

2011 ◽  
Vol 58 (5) ◽  
pp. 535-542 ◽  
Author(s):  
Huanjun Pan ◽  
Dongye Li ◽  
Fang Fang ◽  
Dan Chen ◽  
Lingling Qi ◽  
...  
2018 ◽  
Vol 97 ◽  
pp. 551-556 ◽  
Author(s):  
Yijia Xiang ◽  
Shiyong Ye ◽  
Changhong Cai ◽  
Junchong Chen ◽  
Xuyong Zhao ◽  
...  

2018 ◽  
Vol 25 (3) ◽  
pp. 174
Author(s):  
Monika Bartekova ◽  
Kristina Ferenczyova ◽  
Jana Radosinska ◽  
Dezider Pancza ◽  
Miroslav Barancik ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Huaying Fan ◽  
Liu Yang ◽  
Fenghua Fu ◽  
Hui Xu ◽  
Qinggang Meng ◽  
...  

Salvianolic acid A (SAA), one of the major active components of Danshen that is a traditional Chinese medicine, has been reported to possess protective effect in cardiac diseases and antioxidative activity. This study aims to investigate the cardioprotection of SAAin vivoandin vitrousing the model of myocardial ischemia-reperfusion in rat and hydrogen peroxide (H2O2)-induced H9c2 rat cardiomyoblasts apoptosis. It was found that SAA significantly limited infarct size of ischemic myocardium when given immediately prior to reperfusion. SAA also significantly suppressed cellular injury and apoptotic cell death. Additionally, the results of western blot and phospho-specific antibody microarray analysis showed that SAA could up-regulate Bcl-2 expression and increase the phosphorylation of proteins such as Akt, p42/p44 extracellular signal-related kinases (Erk1/2), and their related effectors. The phosphorylation of those points was related to suppress apoptosis. In summary, SAA possesses marked protective effect on myocardial ischemia-reperfusion injury, which is related to its ability to reduce myocardial cell apoptosis and damage induced by oxidative stress. The protection is achieved via up-regulation of Bcl-2 expression and affecting protein phosphorylation. These findings indicate that SAA may be of value in cardioprotection during myocardial ischemia-reperfusion injury, which provide pharmacological evidence for clinical application.


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