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三甲氧苄嗪对低温保存大鼠离体心脏的保护作用 被引量:2

The protective effect of trimetazidine on rat hearts during cold storage
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摘要 目的:研究三甲氧苄嗪(10-6M)对离体心脏低温保存的影响,并探讨其作用机制。方法:以改良的Langendorff离体鼠心灌注模型,观察三甲氧苄嗪加入UW液后(三甲氧苄嗪-10-6M),离体鼠心在4℃保存6小时后血流动力学、冠脉流出液心肌酶漏出量、心肌含水量、心肌ATP、MDA含量、心肌超微结构的变化。结果:UW液加入三甲氧苄嗪组与未加入三甲氧苄嗪组相比,复灌后心功能恢复率明显增高(P<0.01); 心肌含水量(P<0.05)及丙二醛含量较低(P<0.01);心肌酶漏出量明显减少(P<0.01);心肌ATP水平得到很好地维持(P<0.01);心肌超微结构尤其是线粒体结构改变轻,损伤小。结论:10-6M三甲氧苄嗪对低温保存的大鼠心脏具有明显的保护作用。 Objective:To evaluate the effect of 10-6M trimetazidine on rat hearts during cold storage . Methodmodified Langendorff perfused isolated rat heart model , we added trimetazidine to UW solution with its final concentration of 10-6M . After preserved in the UW solution with or without trimetazidine at 4℃ for 6 hours , the following items were observed in the hearts. the changes of hemodynamics , myocardial enzyme leakage in the coronary effluent , myocardial tissue ATP content , MDA content , myocardial water content and the ultrastructural changes of myocardium . Results:Compared myocardium in UW solution , the hearts in UW solution containing 10-6M trimetazidine had higher recovery rate of cardiacfunction and myocardial tissue ATP content (P<0.01) , lower myocardial water content (P<0.05) , myocardial tissue MDAcontent and myocardial enzyme leakage (P<0.01) , slighter ultrastructural change of myocardium, especially the mitochondrialdamage . Conclusions:Trimetazidine(10-6M) could protect the hypothermically preserved rat heart.
出处 《黑龙江医药科学》 2001年第5期8-9,共2页 Heilongjiang Medicine and Pharmacy
关键词 心脏 低温保存 三甲氧苄嗪 离体心脏 心脏移植 heart cold storage trimetazidine
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参考文献7

  • 1[1]Guamieri C, Finelli C, Zini M et al. Effects of trimetazidine on the calcium transport and oxidative phosphorylation of isolated rat heart mitochondria. Basic Res Cardiol 1997; 92:90-95
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同被引文献18

  • 1朱晓峰,邹志田.中度低温下犬主动脉阻断不同时间脊髓缺血损伤观察[J].黑龙江医药科学,2005,28(4):42-43. 被引量:2
  • 2Mody FV, Singh BN, Dphil, et al. Trimetazidine- inducden- hancement of myocardial glucose utilization in normal and ischemie myocardial tissue : an evaluation by positron emission tomography [J]. Am J Cardiol,2005,82 : 42k -49k.
  • 3Allibardi S, Chierchia SL, Margonato V, et al. Effects of trimetazidine on metabolic and functional recovery of postischemie rat hearts[J]. Cardiovasc Drugs Ther, 2008,12 : 543-549.
  • 4Detry JM, Sellier P, Pennafores, etal. Trimetazidine: a new con- cept in the treament of angina. Comparision. with propranolol in patients with stable angina[J]. Br J Clin Pharmacol, 2004,37:279- 288.
  • 5Boucher FR,Hearse DJ,Opie LH. Effects of trimetazidine on is- chemic contracture in isolated perfused rat hearts[J]. J Cardiovasc Pharmac;ol, 2004,24:45-49.
  • 6Hisatome I, Ishiko R, Tanaka Y, et al. Trimetazidine inhibits Na+,K+-ATPase activity and overdrive hyperpolarization in guinea --pigventricular muscle[J].Eur J Pharmacol, 2001,195:381-388.
  • 7Hugtenburg .IG, Jap TJ, Mahy MJ ,et al. Cardioprotective effect of trimetazidine and nifedipine in guinea--pig hearts subjected to is- chemia[J]. Areh Int Pharmacodyn, 2009,300 : 196-208.
  • 8Guarnieri C,Finelli C,zini M, et al. Effects of trimetazidine on the calcium transport and oxidative phosphorylation of isolated rat heart mitochondria[J]. Basic Res Cardiol, 2007,92 : 90-95.
  • 9Lavanchy N, Martin J, Rossi A. Anti- ischemic effects of trimetazidine: 31P--NMR spectroscopy in the isolated rat heart [J]. Arch Int Pharmacodyn, 2007,286 : 97-110.
  • 10Fantini E, Damaision L, Sentex E, et al. Some biochemical aspects of the protective effect of trimetazidine on rat cardiomyocytes during hypoxia and reoxygenation[J]. J Mol Cell Cardiol, 2004,26 : 949- 958.

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