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1.
Asian Pacific Journal of Tropical Medicine ; (12): 280-284, 2014.
Article in English | WPRIM | ID: wpr-819688

ABSTRACT

OBJECTIVE@#To investigate the effect of salvianolic acid B on rats with myocardial ischemia-reperfusion injury.@*METHODS@#SD rats were randomly divided into five groups (n=10 in each group): A sham operation group, B ischemic reperfusion group model group, C low dose salvianolic acid B group, D median dose salvianolic acid B group, E high dose salvianolic acid B group. One hour after establishment of the myocardial ischemia-reperfusion model, the concentration and the apoptotic index of the plasma level of myocardial enzymes (CTn I, CK-MB), SOD, MDA, NO, ET were measured. Heart tissues were obtained and micro-structural changes were observed.@*RESULTS@#Compared the model group, the plasma CTn, CK-MB, MDA and ET contents were significantly increased, NO, T-SOD contents were decreased in the treatment group (group C, D, and E) (P<0.05); compared with group E, the plasma CTn I, CK-MB, MDA and ET levels were increased, the NO, T-SOD levels were decreased in groups C and D (P<0.05). Infarct size was significantly reduced, and the myocardial ultrastructural changes were improved significantly in treatment group.@*CONCLUSIONS@#Salvianolic acid B has a significant protective effect on myocardial ischemia-reperfusion injury. It can alleviate oxidative stress, reduce calcium overload, improve endothelial function and so on.


Subject(s)
Animals , Rats , Apoptosis , Benzofurans , Pharmacology , Creatine Kinase, MB Form , Blood , Heart , Myocardial Reperfusion Injury , Drug Therapy , Pathology , Myocardium , Cell Biology , Pathology , Myocytes, Cardiac , Nitric Oxide , Blood , Oxidoreductases , Blood , Protective Agents , Pharmacology , Rats, Sprague-Dawley , Troponin I , Blood
2.
Asian Pacific Journal of Tropical Medicine ; (12): 228-231, 2013.
Article in English | WPRIM | ID: wpr-820536

ABSTRACT

OBJECTIVE@#To explore mechanism and protective effect of rosiglitazone on myocardial ischemia reperfusion (I/R) injury.@*METHODS@#A total of 48 male Japanese white big-ear rabbits were randomly divided into control group (A), I/R group (B), low dose of rosiglitazone group (C), high dose of rosiglitazone group (D). Plasma concentration of and also reduced the concentration of plasma serum creatine kinase (CK), CK-MB, high-sensitivity C-reactive protein (hsCRP), ultra-superoxide dismutase (SOD), malondialdehyde (MDA), lactic acid glutathione skin peroxidase (GSH-PX), nitric oxide (NO) and endothelin (ET) were measured 1 h later after I/R. Twenty-four hours after I/R the hearts were harvested for pathological and ultrastructural analysis. Area of myocardial infarction were tested.@*RESULTS@#Plasma concentration of CK, CK-MB, hsCRP, NO, MDA and ET were decreased in C, D group compared with group B. Plasma concentration of T-SOD and GSH-Px were increased significantly in C, D group compared with group B. Compared with group B, pathological and ultrastructural changes in C and D group were slightly. There was significant difference in myocardial infarction area between group C, D and group B (P<0.05). Myocardial infarction area and arrhythmia rate were lower in group C, D compare with group B.@*CONCLUSIONS@#Rosiglitazone may protect myocardium from I/R injury by enhancing T-SOD and GSH-Px concentration, inhibit inflammatory reaction, and improve endothelial function.


Subject(s)
Animals , Male , Rabbits , C-Reactive Protein , Metabolism , Creatine Kinase , Blood , Creatine Kinase, MB Form , Blood , Disease Models, Animal , Endothelins , Blood , Glutathione Peroxidase , Metabolism , Heart , Hypoglycemic Agents , Pharmacology , Malondialdehyde , Blood , Myocardial Reperfusion Injury , Blood , Myocardium , Nitric Oxide , Blood , Rosiglitazone , Superoxide Dismutase , Blood , Thiazolidinediones , Pharmacology , Treatment Outcome
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