The protective effect and mechanism of edaravone against myocardium reperfusion injury in rats
Yingying Cong
Abstract
Yingying Cong
Abstract
Objective To investigate the protective effect and mechanism of edaravone against myocardium reperfusion injury in rats.Methods Twenty-four Wistar rats were randomly divided into control group,ischemia-reperfusion group and protective group.After experiment,the activity of CK-MB,GSH-PX and concentration of MDA were detected.The myocardial morphology was observed with light microscope.TUNEL staining and immunohistochemical methods were used to determine apoptosis of myocardial cells and expression of Bcl-2 and Bax proteins.Results The activity of serum CK-MB and MDA were higher and the activity of GSH-PX was lower in ischemiareperfusion group than in control group.The activity of serum CK-MB and content of MDA were lower and the activity of GSH-PX was higher in protective group than in ischemia-reperfusion group.There was large area of myocardial infarction in ischemia-reperfusion group;but the myocardial injury was lighter in protective group.Apoptotic cells was less in protective group than in ischemia-reperfusion group.Bcl-2,Bax protein and the ratio of Bax/Bcl-2 were significantly higher in ischemia-reperfusion group than in control group (P 0.01),the expression of protein Bcl-2 was significantly higher in protective group than in ischemia-reperfusion group (P 0.01),but the expression of protein Bax and ratio of Bax/Bcl-2 were significantly lower in protective group than in ischemia-reperfusion group,and was higher in ischemia-reperfusion group than in control group.Conclusions Edaravone can reduce the extent of myocardial injury,the mechanism is concerned with reducing free radical damage and inhibiting myocardial cell apoptosis.
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Objective To investigate the protective effect and mechanism of edaravone against myocardium reperfusion injury in rats.Methods Twenty-four Wistar rats were randomly divided into control group,ischemia-reperfusion group and protective group.After experiment,the activity of CK-MB,GSH-PX and concentration of MDA were detected.The myocardial morphology was observed with light microscope.TUNEL staining and immunohistochemical methods were used to determine apoptosis of myocardial cells and expression of Bcl-2 and Bax proteins.Results The activity of serum CK-MB and MDA were higher and the activity of GSH-PX was lower in ischemiareperfusion group than in control group.The activity of serum CK-MB and content of MDA were lower and the activity of GSH-PX was higher in protective group than in ischemia-reperfusion group.There was large area of myocardial infarction in ischemia-reperfusion group;but the myocardial injury was lighter in protective group.Apoptotic cells was less in protective group than in ischemia-reperfusion group.Bcl-2,Bax protein and the ratio of Bax/Bcl-2 were significantly higher in ischemia-reperfusion group than in control group (P 0.01),the expression of protein Bcl-2 was significantly higher in protective group than in ischemia-reperfusion group (P 0.01),but the expression of protein Bax and ratio of Bax/Bcl-2 were significantly lower in protective group than in ischemia-reperfusion group,and was higher in ischemia-reperfusion group than in control group.Conclusions Edaravone can reduce the extent of myocardial injury,the mechanism is concerned with reducing free radical damage and inhibiting myocardial cell apoptosis.
Key concepts: Edaravone, Ischemia, Medicine, Reperfusion injury, TUNEL assay, Apoptosis, BAX Protein, Immunohistochemistry