目的:探讨人参皂苷Rg1对离体大鼠心缺血/再灌注(I/R)损伤的保护作用。方法:选取SPF级SD大鼠随机分为正常对照组、I/R组、人参皂苷Rg1(1、5、10、20μmol/L)处理组。利用Langendorff灌流系统建立大鼠离体心I/R损伤模型。Lab Chart电生理系统实时监测心功能指标,血清生化检测心流出液中心肌酶含量,TTC染色法测定心肌梗死面积。结果:不同浓度人参皂苷Rg1均可改善心肌I/R损伤引起的左室发展压(LVDP)和左室内上升/下降最大速率(±dp/dtmax)的下降,并降低流出液中乳酸脱氢酶(LDH)、肌酸激酶同工酶(CK-MB)、肌红蛋白(MYO)和肌钙蛋白-I(TroI)的含量,显著减少心肌梗死面积。其中5μmol/L和10μmol/L浓度的人参皂苷Rg1对心的保护作用最显著。结论:人参皂苷Rg1具有药物预适应作用,改善心肌I/R损伤后的心肌生理功能,减少流出液中心肌酶的释放和心肌梗死面积,从而发挥抗心肌I/R损伤的保护作用。
Objective: To investigate the mechanism of ginsenoside Rg1 protecting against myocardial ischemia/reperfusion (I/ R) injury in isolated rat heart. Methods: SPF Sprague Dawley rats were randomly divided into control group, I/R group, and ginsenoside Rg1 precondition group which was further divided into four sub-groups by different dosage of administration(1, 5, 10 and 20μmol/L). Myocardial I/R injury models of isolated rat heart were established by Langendorff perfusion system. Cardiac function index was measured with Lab Chart real-time monitoring system; the content of myocardial enzymes in the outflowing liquid of the heart was measured by serum biochemical test; TTC staining method was used to determine myocardial infarct size. Results: Ginsenoside Rg1 of all the four different concentrations improved the decrease of the left ventricular developed pressure and peak systolic/diastolic left ventricular rate arising from myocardial I/R injury, and reduced the content of lactate dehydrogenase, creatine kinase;isoenzyme, myoglobin and troponin-I, thus significantly decreasing the area of cardial infarction. The 5μmol/L and 10μmol/L ginsenoside Rg1 precondition groups protected the heart most significantly. Conclusion: Ginsenoside Rg1 demonsttrates pharmacological preconditioning effect and protects against myocardial I/R injury, which improves myocardial physiological function and reduces myocardial enzyme leakage in post myocardial I/R injury, thereby reducing the myocardial infarction size.