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作 者:王道成[1,2] 李七一[3] 朱萱萱[4] 严士海[4] 秦晓康[4] 马俊杰[4]
机构地区:[1]南京中医药大学,南京210029 [2]江苏省扬州市中医院,江苏扬州225009 [3]江苏省中医院,南京210029 [4]江苏省中医院药理实验室,南京210029
出 处:《中国实验方剂学杂志》2010年第10期143-146,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:康缘中医药科技创新基金项目(HZ0803KY)
摘 要:目的:观察冠心平对异丙肾上腺素(ISO)致大鼠心肌缺血的影响。方法:采取大鼠scISO(30mg·kg-1)致急性心肌缺血模型,观察冠心平对大鼠血清乳酸脱氢酶(LDH)、肌酸磷酸激酶(CK)、丙二醛(MDA)、超氧化物歧化酶(SOD)活性的影响;观察注射ISO后不同时间J点下降情况,心肌病理损伤程度的影响;结果:冠心平各剂量组均可不同程度降低LDH,CK活力降低血清MDA水平,升高SOD水平(P<0.01,P<0.05);明显抑制ISO引起的大鼠心电图J点下降(P<0.05,P<0.01);心肌病理损伤程度明显减轻。结论:冠心平对ISO致大鼠心肌缺血模型具有明显保护作用。Objective:To observe the effect of Guanxinping on myocardial ischemic injury induced by isoprenaline in rats. Method:Rat myocardial ischemia was induced by subcutaneous injection of isoprenaline(30 mg·kg^ -1 ). The effect of Guanxinping on the lactate dehydrogenase ( LDH),serum creatine kinase ( CK),malondial dehyde (MDA)and superoxide dismutase (SOD)was observed. The descent of J point at different time after injection of isoprenaline was examined,and pathological investigation of myocardial injury in rats was carried out. Result:Guanxinping could obviously inhibit the activities of serum CK,LDH,and MDA ,enhance serum SOD activity(P 〈0. 01,P〈 0. 05). Guanxinping could inhibit descent of J point in rat myocardial ischemia induced by isoprenaline( P〈 0. 05,P〈 0. 01 ),and significantly reduce the extent of myocardial pathological damage. Conclusion:Guanxinping can obviously ameliorate myocardial ischemic injury induced by isoprenaline in rat.
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