›› 1998, Vol. 18 ›› Issue (2): 69-72.

• 论文 • 上一篇    下一篇

地塞米松对大鼠离体心脏再灌注损伤保护机制的研究

  

  1. 上海第二医科大学附属仁济医院心胸外科,上海 200001
  • 收稿日期:1997-12-08 出版日期:1998-04-25 发布日期:2013-03-19

Mechanism of Protective Effect of Dexamethasone on Myocardial Reperfusion Injury in Isolated Working Rat Heart

  1. Department of Cardiothoraeic Surgery of Affiliated Renji Hospital,Shanghai Second Medical University,Shanghai 200001
  • Received:1997-12-08 Online:1998-04-25 Published:2013-03-19

摘要: 用大鼠的离体工作心脏研究地塞米松对心肌再灌注损伤保护作用的机制。30只SD大鼠随机等分为对照组1、对照组2和实验组,均制备离体工作心脏模型。对照组2和实验组继续进行缺血再灌注实验,心脏停跳前从主动脉根部灌注冷晶体停搏液,但实验组的停搏液中加用地塞米松(20μmol/L)。心脏停跳前及再灌注30min时分别监测心功能,测定冠脉流出液的一氧化氮(NO)和肌酸磷酸激酶(CPK),及心肌组织的NO合酶(NOS)和丙二醛(MDA)。结果:心脏再灌注后,对照组2与对照组1相比较,结构型NOS(cNOS)活性下降,诱导型NOS(iNOS)活性升高,NO量减少;实验组与对照组2相比,i-NOS活力下降,而cNOS活性变化不显著,NO分泌减少,并且心功能恢复率提高,MDA、CPK下降。这提示,地塞米松可能通过下调iNOS表达,减少NO生成,而对心肌再灌注损伤产生保护作用。

关键词: 地塞米松, 再灌注损伤, 心肌保护, 大鼠, 离体心脏

Abstract: To study the mechanism of protective effect of dexamethasone on myocardial reperfu-sion injury,the isolated working heart models were prepared in 30 SD rats,and then divid-ed into 3 groups:normal control group (gruop 1), ischemia and reperfusion control group (group 2) and experimental group (group 3). Cold crystalloid cardioplegic solution was perfused into the aorta of group 2 and 3 before cardiac arrest.Dexamethasone was added to the cardioplegic solution in group 3 at the concentration of 20 μmol/L. The levels of nitric oxide (NO) and creatine phosphokinase (CPK) in the blood of coronary sinus,and of NO synthase (NOS) and malondialdehyde (MDA) in myocardium were measured before arrest and 30 min after coronary reperfusion. The cardiac function was assessed at the same cor-responding times. The results showed that in group 2,as compared with group1,the levels of NO and constitutive NOS (cNOS) were reduced and inducible NOS (iNOS) increased after cardiac reperfusion,in the experimental group,as compared with group 2,the levels of NO and iNOS were reduced, while cNOS not significantly changed,and the recovery of cardiac function was ameliorated,the levels of MDA and CPK were reduced. These indicated that dexamethasone was helpful for myocardial protection. The reduction of iNOS and NO induced by dexamethasone may play an important role in myocardial protection.

Key words: Dexamethasone, Reperfusion injury, Myocardial protection, Isolated working heart, Rat