期刊文献+

吡那地尔预处理对不同温度高钾停跳离体兔心的保护作用 被引量:1

Myocardial protective effect of pinacidil pretreatment on isolated rabbit heart arrest induced with high potassium crystalloid cardioplegia at different temperatures
下载PDF
导出
摘要 目的:观察ATP敏感性钾通道开放剂(KCOs)吡那地尔(Pinacidil)药物预处理对不同温度高K+停跳液灌注离体兔心肌的保护效果. 方法:离体兔心24颗以Langendorff模型灌注10 min,随机分成3组:对照组(C组):低温高K+停跳;WP组和CP组为预处理组(停跳前以Pinacidil 10 μmol/L灌注15 min):分别为常温及低温高K+停跳. 全心缺血45 min, C组及CP组心脏停跳期间的温度为26~28℃,WP组为36~38℃. 三组恢复37℃ K-H灌注20 min. 分别测定心脏停、复跳时间,心率、心律、左心室内压(LVP)及收缩力、心肌腺苷酸及脂质过氧化物丙二醛(MDA)含量,检查心肌光镜结构. 结果:三组心脏停跳时间无明显差异,预处理组复跳迅速,两组间无显著差异,C组复跳缓慢,与预处理组比较差异有显著性(P<0.05);再灌注后CP组较WP及C组心肌收缩力与LVP恢复较快(P<0.05),而WP组LVP又比C组恢复好(P<0.05). 预处理组心肌组织腺苷酸,总腺苷酸(TAN)、细胞能荷(EC)显著高于C组(P<0.01),CP组又明显高于WP组(P<0.01或P<0.05),预处理组的心肌结构也明显好于C组,CP组又好于WP组. 三组MDA含量无显著差异. 结论:Pinacidil预处理能显著增强离体兔心肌缺血/再灌注的保护效果,对低温停跳心脏的保护效果更佳. AIM: TO evaluate the myocardial protective effect of pinacidU pretreatment on isolated rabbit hearts arrested with high potassium crystalloid cardioplegic solution at different temperatures. METHODS: Twenty-four rabbit hearts were randomly divided into 3 groups: control group (group C, hypotherrnic hyperkalemic cardiac cardioplegia) and pinacidil pretreatment groups [ warm pretreatment group (WP) and cold pretreatment group (CP), i.e., normothermic pretreatment and hypothermic pretreatment respectively]. Isolated rabbit hearts (group C) were perfused with oxygenated Krebs-Henseleits solution (K-H) by Langendorff apparatus for 10 min, followed with the standard 4℃ St. Thomas solution ( K^+ 16 mmol/L at 37℃ ) cardioplegia. In group WP and group CP, when the hearts were perfused with K-H for 10 min, K-H solution containing pinacidil 10 μmol/L (37℃ in group WP, 4℃ in group CP) pretreatment was carried out before the standard St. Thomas (37℃ in group WP, 4℃ in group CP) was perfused. The hearts were subjected to 45 min ischemia (group C and group CP, 26 -28℃; group WP, 36 -38℃) and followed by 20 min reperfusion with 37℃ K-H solution. The time of heart arrest and rebeating, heart rate, heart rhythm, left ventricle pressure, left ventricle pressure (LVP), myocardial adenylate and malondialdehyde (MDA) level were analyzed respectively. The myocardial structure of microscopic structure was determined. RESULTS: The time of heart arresting was not different in the 3 groups. The rate of rebeating after aortic unclamping was faster in pretreatment groups than that in group C ( P 〈 0. 05 ), but it was significant different between the 2 pretreatment groups. Recoveries of left ventricle pressure and LVP were more rapid in group CP than those in group WP or group C ( P 〈 0. 05). The recovery of LVP was better in group WP than that in group C (P〈0.05). The levels of ATP, TAN and EC were the highest in group CP, the lowest levels in group C, and in-between in group WP. Myocardial microscope structure was the best in the group CP, then in group WP and group C in a descending order. MDA content was not significantly different in the 3 groups. CONCLUSION: Pinacidil pretreatment may remarkably enhance the myocardial protection against ischemia/reperfusion injury on the isolated hearts arrested with high potassium crystalloid and has a better protective effect on hypothermic cardiac cardioplegia.
出处 《第四军医大学学报》 北大核心 2005年第22期2053-2056,共4页 Journal of the Fourth Military Medical University
基金 国家自然科学基金(39760071)
关键词 吡那地尔 预处理 心脏停搏 人工 心肌再灌注损伤 pinacidil pretreatment heart arrest, induced myocardial reperfusion injury
  • 相关文献

参考文献13

  • 1Kavianipour M, Ronguist G, Wiskstrom G, et al. Ischaemic preconditioning alters the energy metabolism [J]. Acta Physiol Scand, 2003;178(2):129-137.
  • 2Mullenheim J, Schlack W, Frassdorf J, et al. Additive protective effects of late and early ischemic preconditioning are mediated by the opening of KATP channels in vivo [J]. Pflugers Arch, 2001;422(2):178-187.
  • 3Zhu HF, Dong JW, Zhu WZ, et al. ATP-dependent potassium channels involved in the cardiac protection induced by intermittent hypoxia against ischemia/reperfusion injury [J]. Life Sci, 2003;73(10):1275-1287.
  • 4Wang X, Wei M, Kuukasjarri P, et al. Novel pharmacological preconditioning with diazoxide attenuates myocardial stunning in coronary artery bypass grafting [J]. Eur J Cardiothorac Surg, 2003;24(6):967-973.
  • 5阳世光,喻田,余志豪,刘兴奎,叶英.吡那地尔预处理对体外循环犬心肌的保护效果[J].中华麻醉学杂志,2003,23(7):508-510. 被引量:2
  • 6Crestaneffo JA, Dofiba NM, Babsky AM, et al. Opening of potassium channels protects mitochondrial function from calcium overload [J]. J Surg Res, 2000;94(2):116-123.
  • 7Baczko I, Giles WR, Light PE. Pharmacological activation of plasma-membrane KATP channels reduces reoxygenation-induced Ca2+ overload in cardiac myocytes via modulation of the diastolic membrane potential [J]. Br J Pharmacol, 2004;141(6):1057-1059.
  • 8Lembert N, Idahl La, Ammon HP. K-ATP channel independent effects of pinacidil on ATP production in isolated cardiomyocyte or pancreatic beta-cell mitochondria [J]. Biochem Pharmacol, 2003;65(11):1835-1844.
  • 9刘军叶,郭鹞,郑振兴,曾桂英,王晋.电磁脉冲对小鼠脾细胞Fas和FasL mRNA表达的影响[J].第四军医大学学报,2001,22(7):648-651. 被引量:5
  • 10程何祥,张荣庆,马颖艳,徐凯,贾国良,赵新国,李飞.吡那地尔对大鼠心肌缺血/再灌注时细胞凋亡及fas基因表达的影响[J].第四军医大学学报,2002,23(22):2067-2070. 被引量:4

二级参考文献21

  • 1Grover GJ, Newburger J, Sleph PG, et al . Cardioprotective effects of the potassium channel opener cromakalim: stereoselectivity and effects on myocardial adenine nucleotides. J Pharmacol Exp Ther, 1991,257: 156-162.
  • 2Atkinson DE. The energy charge of the adenylate pool as a regulatory parameter: interaction with feedback modifiers. Biochemistry, 1968, 7:4030-4034.
  • 3Hosoda H, Sunamori M, Suzuki A. Effects of pinacidil on rat hearts undergoing hypothermic cardioplegia. Ann Thorac Surg, 1994, 58: 1631-1636.
  • 4Mcpherson CD, Pierce GN, Cole WC. Ischemic cardioprotection by ATP-sensitive K+ channels involves high-energy phosphate preservation. Am J Physiol Soc, 1993,265: H1809-1818.
  • 5InoIne I, Nagase H, Kishi K, et al. ATP-sensitive K + channels in the mitochondrial inner member. Nature,1991, 352: 244-247.
  • 6Grover G J, Sleph PG, Dzwonczyk S . Pharmacologic profile of cromakalim in the treatment of myocardial ischemia in isolated rat hearts and anesthetized dogs. J Cardiorasc Pharmacol, 1990, 16: 853-864.
  • 7Qiu Y, Galinanes M, Hearse DJ. Protective effect of nicorandil as an additive to the solution for continuous warm cardioplegia. J Thorac Cardiovasc Surg, 1995,110 : 1063-1072.
  • 8Thuringer D, Escande D. Apparent competition between ATP and potassium channel opener, RP49356, on ATP-sensitive K+ channels of cardiac myocytes. Mol Pharmacol, 1989,36: 897-902.
  • 9Ren D Q,第四军医大学学报,2000年,21卷,3期,289页
  • 10Zhang Y P,第四军医大学学报,2000年,21卷,2期,223页

共引文献8

同被引文献12

  • 1刘蔚,汪海,肖文彬.吡那地尔与硝苯啶对大鼠离体工作心脏的影响[J].军事医学科学院院刊,1996,20(2):94-96. 被引量:6
  • 2高敏,汪海.新型钾通道开放剂对心血管ATP-敏感性钾通道基因表达的调节作用[J].中国应用生理学杂志,2006,22(4):451-454. 被引量:3
  • 3Chen YP, Qiu CR, Wang H. Cardiovascular pharmacological characterization of novel 2,3-dimethmyl-2-butylamine derivatives in rats [J].Life Sci, 2004, 75(17): 2131 -2142.
  • 4Wang H. Pharmacological characteristics of the novel antihypertensive drug iptakalim hydrochloride and its molecular mechanisms [ J ]. Drug Dev Res, 2003, 58:65 -68.
  • 5Wang H, Tang Y, Wang L, et al. ATP-sensitive potassium channel openers and 2,3-dimethyl-2-butylamine derivatives [ J ]. Curr Med Chem, 2007, 14:133-155.
  • 6Wang H, Long CL, Zhang YL. A new ATP-sensitive potassium channel opener reduces blood pressure and reverses cardiovascular remodeling in experimental hypertension[J]. J Pharmacol Exp Ther, 2005, 312:1326-1333.
  • 7Xue H, Zhang YL, Liu GS, et al. A new ATP-sensitive potassium channel opener protects the kidney from hypertensive damage in spontaneously Hypertensive rats [ J ]. J Phannacol Exp Ther, 2005, 315: 501 -509.
  • 8Wang H, Zhang YL, Chen YP. Targeting small arteries of hypertensive status with novel ATP-sensitive potassium channel openers[ J]. Curr Vasc Pharmacol, 2005, 3 (2) : 119 -124.
  • 9Grover GJ. Protective effects of ATP-sensitive potassium channel openers in experimental myocardial ischemia [ J] . J Cardiovasc Pharmacol,1994,24 (Suppl 4) :S 18 -27.
  • 10刘蔚,龙超良,路新强,肖文彬,汪海.盐酸埃他卡林对大鼠离体工作心脏功能的影响[J].中国药理学通报,2002,18(3):349-351. 被引量:14

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部