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中国临床药理学与治疗学 ›› 2005, Vol. 10 ›› Issue (8): 921-924.

• 研究原著 • 上一篇    下一篇

甘草酸二铵对大鼠心肌缺血再灌注损伤脂质过氧化及心肌酶活性的影响

余修洪, 李远重1, 蒋建刚2   

  1. 武汉市八医院南院心血管内科, 武汉 430014, 湖北;
    1咸宁市中心医院心血管内科, 2咸宁学院医学院内科教研室, 咸宁 437100, 湖北
  • 收稿日期:2005-03-30 修回日期:2005-05-18 发布日期:2020-11-22
  • 通讯作者: 李远重,男,主任医师,主要从事内科心血管冠心病的临床研究。Tel:0715-8169099
  • 作者简介:余修洪,男,副主任医师,主要从事内科心血管冠心病的临床研究工作。Tel:027-62525122
  • 基金资助:
    湖北省优秀中青年资助项目(No99B018)

Effects of dammonii glycyrrhizinatis on lipid peroxidation and enzyme activity in ischemia-reperfusion myocardium rats

YU Xiu-hong, LI Yuan-zhong1, JIANG Jian-gang2   

  1. Department of Cardiology, the Eighth Hospital of Wuhan City, Wuhan 430014, Hubei, China;
    1Department of Cardiology, Xianning Center Hospital, Xianning 437100, Hubei, China;
    2Department of Internal Medicine, Xianning Medical College, Xianning 437100, Hubei, China
  • Received:2005-03-30 Revised:2005-05-18 Published:2020-11-22

摘要: 目的: 观察甘草酸二铵(DG)对大鼠心肌缺血再灌注损伤脂质过氧化及心肌酶活性的影响。方法: 雄性wistar大鼠30只,随机分为假手术组、缺血再灌注组和DG20mg·kg-1组。每组10只。采用在体大鼠心肌缺血30min再灌注60min损伤模型,再灌注60min后分别用比色法测定心肌丙二醛(MDA)含量、超氧化物歧化酶(SOD)、三磷酸腺苷酶(ATP酶)、血清磷酸肌酸激酶(CPK)和乳酸脱氢酶(LDH)水平,并用酶组织化学方法检测心肌组织琥珀酸脱氢酶(SDH)的活性。结果: DG能显著降低心肌组织中MDA含量和SDH的活性(P<0.05,P<0.01),提高SOD和ATP酶活性(P<0.05,P<0.01),并减少心肌CPK和LDH的释放(P<0.05,P<0.01)。结论: DG具有保护大鼠心肌缺血再灌注损伤的作用,其作用机理可能与其降低心肌脂质过氧化,增强心肌细胞SOD、SDH和ATP酶活性有关。

关键词: 甘草酸二铵, 心肌再灌注损伤, 超氧化物歧酶, 三磷酸腺苷酶, 琥珀酸脱氢酶

Abstract: AIM: To study effects of dammonii glycyrrhizinatis (DG) on lipid peroxidation and enzyme activity in the ischemia-reperfusion myocardium rats. METHODS:30 male Wistar rats were divided into 3 groups:sham group, ischemia-reperfusion group and DG group (20 mg·kg-1) (n = 10).Myocardial ischemia reperfusion injury model was produced by the 30 min ligation of left descending coronary artery (LAD) and 60 min reperfusion in rats.The content of myocardial malondialdehyde (MDA), the activities of myocardial superoxide dismutase (SOD), adenosinetriphosphatase (ATPase) and plasma lactate dehydrogenase (LDH), creative phosphokinase (CPK) level were measured by colorimetry, and the activities of succinate dehydrogenase (SDH) were measured by histochemical stain after reperfusion.RESULTS: DG significantly reduced myocardium MDA content (P <0.05 or P <0.01), enhanced the activities of SOD, ATPase and SDH (P <0.05, P <0.01) and decreasedmyocardial LDH and CK release (P <0.05 or P <0.01).CONCLUSION: DG can protect myocardium against ischemia-reperfusion injury, and its mechanism may be related to the reduction of myocardial lipid peroxidation, the enhancement of SOD, SDH and ATPase activities.

Key words: diammonii glycyrrizinatis, myocardial reperfusion injury, superoxide dimutase, adenosinetriphosphatase, succinate dehydrogenase

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