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尼可地尔超极化心脏停搏心肌保护剂量-效应关系的实验研究 被引量:1

Experimental study on the dose-response relation of myocardial protection: hyperpolarized cardioplegic arrest with nicorandil
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摘要 目的 :对不同浓度尼可地尔心肌麻痹液超极化心脏停搏心肌保护的剂量 -效应关系进行研究 ,选择最适心肌保护剂量。 方法 :实验分 6组 ,即对照组 (去极化心脏停搏组 )、5种不同浓度 (2 5、5 0、10 0、12 5和 15 0 μm ol/L)尼可地尔超极化心脏停搏组。 4℃心肌麻痹液 (40 ml/kg)诱停离体鼠心 ,每隔 30 min重复灌注心肌麻痹液 (2 0 m l/kg) ,(15± 1)℃心脏停搏 12 0 m in后再灌注 ,离体心工作 30 min。记录心脏机械停搏时间、再灌注后心脏复跳情况、心功能恢复 (左室发展压、主动脉流量及左室压力微分 )、冠状循环灌注平均流量、心肌丙二醛 (MDA )含量、心肌超微结构的改变。 结果 :尼可地尔心肌麻痹液心肌保护呈类似抛物线形的剂量 -效应关系。尼可地尔浓度为 10 0μmol/L时 ,L VDP的恢复率最佳 ,心肌保护效果最好。 结论 :尼可地尔超极化心脏停搏心肌保护的最适心肌保护剂量为 10 0μm ol/ L。 Objectives:Dose response effect of nicorandil cardioplegia at various concentrations was studied to optimize its myocardial protective effect. Methods: Forty eight isolated working rat hearts were divided into 6 groups randomly. They were group A: control (depolarized cardiac arrest with St. Thomas solution No.2), group B,C,E,F and G: hyperpolarized cardiac arrest (nicorandil concentration were 25,50,100,125 and 150μmol/L respectively). The hearts underwent a 120 minute hypothermic arrest (15±1)℃ with cardioplegia (40 ml/kg) and reinfused with cardioplegia (40 ml/kg) at interval of 30 minutes. Mechanical arrest time, cardiac functional recoveries, myocardial content of malondialdehyde (MDA) and ultrastructure were measured. Results:The protective effect of nicorandil cardioplegia was dose related. Conclusions:The optimal concentration of nicorandil in cardiplegia may be 100μmol/L for myocardial protection.
出处 《医学研究生学报》 CAS 2001年第2期139-145,共7页 Journal of Medical Postgraduates
关键词 尼可地尔 心肌保护 超极化心脏停搏 剂量-效应关系 治疗 Nicorandil Myocardial protection Hyperpolarized cardiac arrest Dose response relation
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参考文献9

  • 1Escande D,Cavero I.K+ channel openers and natural cardioprotection[J].Trends Pharmacol Sci,1992,13:269-272
  • 2Damiano RJJ,Cohen NM.Hyperpolarized arrest attenuates myocardial stunning following global surgical ischemia: an alternative to traditional hyperkalemic cardioplegia[J]?J Card Surg,1994,9:517-525.
  • 3周志,有景华,张石江,李德闽,李忠东,周建峰,顾卫东,高声甫.尼可地尔超极化心脏停搏心肌保护的实验研究[J].医学研究生学报,1999,12(1):3-6. 被引量:1
  • 4Noma A.ATP-regulated K+ channels in cardiac muscle[J].Nature,1983,305:147-148.
  • 5Gross GJ,Auchampach JA.Role of ATP dependent potassium channels in myocardial ischaemia[J].Cardiovasc Res,1992;26:1011-1016.
  • 6Taira N.Nicorandil as a hybrid between nitrates and potassium channel activators[J].Am J Cardiol,1989,63:18J-24J.
  • 7Jaywant AM,Lawton JS,Hsia PW,et al.Hyperpolarized cardioplegic arrest with nicorandil: advantages over other potassium channel openers[J].Circulation,1997,96[Suppl Ⅱ]:Ⅱ240-Ⅱ246.
  • 8Cohen NM,Damiano RJJ,Wechsler AS.Is there an alternative to potassium arrest[J]? Ann Thorac Surg,1995.60:858-863.
  • 9Lawton JS,Harrington GC,Allen CT,et al.Myocardial protection with pinacidil cardioplegia in the blood-perfused heart[J].Ann Thorac Surg,1996,61:1680-1688.

同被引文献11

  • 1Tritto I, Ambrosio G. Role of oxidants in the signaling pathway of preconditioning. Antioxid Redox Signal, 2001,3 : 3-10.
  • 2Galagudza M, Kurapeey D, Minasian S, et al. Ischemic postconditioning: brief ischemia during reperfusion converts persistent ventricular fibrillation into regular rhythm. Eur J Cardiothorac Surg, 2004,25 : 1006-1010
  • 3Kin H, Zhao ZQ, Sun HY, et al. Postconditioning attenuates myocardial ischemia-reperfusion injury by inhibiting events in the early minutes of reperfusion. Cardiovasc Res, 2004, 62:74-85.
  • 4Yang XM, Proctor J-B, Cui L, et al. Multiple, brief coronary occlusions during early reperfusion protect rabbit hearts by targeting cell signaling pathways. J Am Coll Cardiol, 2004, 44:1103-1110.
  • 5Zhao ZQ, Corvera JS, Halkos ME, et al. Inhibition of myocardial injury by ischemic postconditioning during reperfusion: comparison with ischemic preconditioning. Am J Physiol Heart Circ Physiol, 2003, 285: H579-H588.
  • 6臧益民,朱妙章,主编.临床心血管生理学及其进展.第1版.北京:世界图书出版社,1993.136—147.
  • 7Dos Santos P, Kowaltowski AJ, Laclau MN, et al. Mechanisms by which opening the mitochondrial ATP-sensitive K^+ channels protects the ischemic heart. Am J Phsiol Heart Circ Phsiol, 2002, 283: H284- H295.
  • 8Holmuhamedov EL, Jovanovic S, Dzeja PP, et al. Mitochondrial ATP- sensitive K^+ channels modulate cardiac mitochondrial function. Am J Physiol, 1998,275: H1567-H1576.
  • 9Fukuda H, Luo CS, Gu X, et al. The effect of KATP channel activation on myocardial cationic and energetic status during ischemia and reperfusion: role in cardioprotection. J Mol Cell Cardiol, 2001, 33: 545-560.
  • 10华鲁纯,孟淑美,杨俭.小肠缺血再灌注损伤时自由基清除剂及MDA变化的实验研究[J].中国微循环,1999,3(4):205-207. 被引量:11

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