The effects of atorvastatin on myocardial no-reflow after ischemia/reperfusion in rats
Zhang Ying-ji
Abstract
Zhang Ying-ji
Abstract
Objective To evaluate the effects of atorvastatin on myocardial no-reflow after ischemia/reperfusion in rats,and to investigate the possible mechanisms.Methods Fifty-six male SD rats were randomly assigned to four groups: shame group,ischemia and reperfusion group,atorvastatin group and atorvastatin+L-NNA group.Pretreatment of gastric lavage with atorvastatin [20 mg/(kg·d)] were given to subjects in atorvastatin group for 3 days.L-NNA(15 mg/kg) intravenous administration 15 minutes before ischemia plus atorvastatin pretreatment was given to subjects in atorvastatin+L-NNA group.All rats,except for those in shame group,received occlusion of left anterior descending artery(LAD) for 60 minutes followed by 120 minutes of reperfusion.Serum CK-MB and myocardial NO were detected after experiment.Different myocardium regions of ischemia,no-reflow and infarction were recognized and assessed according to Evans blue dye,thioflavin S fluorescent dye and triphenyltetrazolium chloride(TTC) staining techniques,respectively.Electronic microscope was applied to observe ultramicrostructures of capillary endothelial cells and myocardial mitochondria.Results Atorvastatin significantly elevated the myocardial NO,reduced CK-MB activity,relieved the microcirculation and myocardial mitochondrial injury,and reduced the no-reflow and necrosis areas(P0.05).However,these effects were reversed by L-NNA.Conclusion Atorvastatin can reduce the area of myocardial no-reflow after ischemia-reperfusion.This beneficial effect is dependant on NO by up-regulating eNOS expression,which activates mitochondrial K-ATP channel and reduces microvascular injury.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To evaluate the effects of atorvastatin on myocardial no-reflow after ischemia/reperfusion in rats,and to investigate the possible mechanisms.Methods Fifty-six male SD rats were randomly assigned to four groups: shame group,ischemia and reperfusion group,atorvastatin group and atorvastatin+L-NNA group.Pretreatment of gastric lavage with atorvastatin [20 mg/(kg·d)] were given to subjects in atorvastatin group for 3 days.L-NNA(15 mg/kg) intravenous administration 15 minutes before ischemia plus atorvastatin pretreatment was given to subjects in atorvastatin+L-NNA group.All rats,except for those in shame group,received occlusion of left anterior descending artery(LAD) for 60 minutes followed by 120 minutes of reperfusion.Serum CK-MB and myocardial NO were detected after experiment.Different myocardium regions of ischemia,no-reflow and infarction were recognized and assessed according to Evans blue dye,thioflavin S fluorescent dye and triphenyltetrazolium chloride(TTC) staining techniques,respectively.Electronic microscope was applied to observe ultramicrostructures of capillary endothelial cells and myocardial mitochondria.Results Atorvastatin significantly elevated the myocardial NO,reduced CK-MB activity,relieved the microcirculation and myocardial mitochondrial injury,and reduced the no-reflow and necrosis areas(P0.05).However,these effects were reversed by L-NNA.Conclusion Atorvastatin can reduce the area of myocardial no-reflow after ischemia-reperfusion.This beneficial effect is dependant on NO by up-regulating eNOS expression,which activates mitochondrial K-ATP channel and reduces microvascular injury.
Key concepts: Atorvastatin, Medicine, Evans Blue, Ischemia, Myocardial infarction, Reperfusion injury, Occlusion, Internal medicine