Key result
Pretreatment with salvianolic acid A improved the 24-hour survival rate to 82% compared to 61% in the control group following myocardial ischemia/reperfusion injury in rats.
Why the study?
Does salvianolic acid A (SAA) reduce myocardial infarct size and improve survival in a rat model of myocardial ischemia/reperfusion injury?
Does salvianolic acid A (SAA) reduce myocardial infarct size and improve survival in a rat model of myocardial ischemia/reperfusion injury?
In a rat model of myocardial ischemia/reperfusion injury, salvianolic acid A significantly reduced infarct size and improved survival by inhibiting platelet aggregation and inflammation.
Answers are grounded in this paper and cite their sources.
Salvianolic acid A may confer survival benefit in rat ischemia/reperfusion models; leaves open translation to human therapy.
The aim of the present study was to investigate the protective effect of salvianolic acid A (SAA) on myocardial ischemia/reperfusion injury in rats. SAA (10 mg/kg) or Tirofiban (60 µg/kg) was administered to rats by jugular vein injection 10 min before the initiation of reperfusion. After 3 h of reperfusion, platelet aggregation was measured using an aggregometer and levels of nitric oxide (NO) were detected using an ultraviolet spectrophotometer. Serum levels of cardiac troponin T (cTnT), creatine kinase isoenzyme MB (CK-MB), p-selectin, interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) were also measured 3 and 24 h after reperfusion. Furthermore, morphology of the ischemic myocardium was histopathologically analyzed by hematoxylin and eosin staining, and the infarct area was evaluated by Evans blue and triphenyltetrazolium chloride staining. In rats subjected to reperfusion, it was observed that pretreatment with SAA significantly increased the survival rate (P<0.05), and that increased survival rate was due to a significant decrease in infarct size, as evidenced by significantly reduced serum levels of cTnT and CK-MB (P<0.05). In addition, decreases in infarct size occurred through the inhibition of platelet aggregation and inflammation associated with reperfusion-induced myocardial cell damage, as indicated by reduced serum levels of p-selectin, TNF-α, IL-1β and NO. In conclusion, SAA was protective against myocardial ischemia/reperfusion injury in rats by serving antiplatelet and anti-inflammation roles.
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Yuan et al. (2017) studied Myocardial ischemia/reperfusion injury (n=150). Salvianolic acid A vs. 5% glucose (I/R control) was evaluated on Survival rate at 24 hours (p=0.033). Pretreatment with salvianolic acid A improved the 24-hour survival rate to 82% compared to 61% in the control group following myocardial ischemia/reperfusion injury in rats.
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