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异氟醚延迟预处理对兔心肌缺血再灌注时αB-晶状体蛋白表达的影响 被引量:1

Effect of isoflurane-induced delayed preconditioning on αB-crystallin expression during myocardial ischemia-reperfusion in rabbits
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摘要 目的探讨异氟醚延迟预处理对兔心肌缺血再灌注时αB-晶状体蛋白表达的影响。方法健康雄性新西兰大白兔30只,体重2.0~2.5kg,随机分为3组(n=10):假手术组(S组)吸入纯氧2h,24h后仅动脉下穿线不结扎;心肌缺血再灌注组(IR组)吸入纯氧2h,24h后行心肌缺血再灌注;异氟醚延迟预处理组(I组)吸入2%异氟醚2h,24h后行心肌缺血再灌注。采用结扎左冠状动脉前降支40min,再灌注120min的方法制备心肌缺血再灌注模型。于再灌注120min时采集动脉血样测定血清超氧化物歧化酶(SOD)活性,取心肌组织测定αB-晶状体蛋白及caspase-3的表达水平,计算心肌缺血面积和梗死面积,观察心肌细胞超微结构。结果s组心肌细胞完整,排列整齐,线粒体形态正常,糖原丰富;IR组心肌细胞水肿,心肌纤维排列紊乱,线粒体、内质网膜肿胀,空泡化;I组心肌细胞水肿程度减轻,心肌纤维排列较完整,线粒体轻度肿胀。与IR组比较,I组心肌梗死面积减小,血清SOD活性升高,心肌caspase-3表达下调,αB-晶状体蛋白表达上调(P〈0.05)。结论异氟醚延迟预处理减轻兔心肌缺血再灌注损伤的机制可能与上调心肌αB-晶状体蛋白表达有关。 Objective To investigate the effect of isoflurane-induced delayed preconditioning on αB-crystallin expression during myocardial ischemia-reperfusion (I/R) in rabbits. Methods Thirty male New Zealand white rabbits weighing 2.0-2.5 kg were randomly assigned into 3 groups ( n = 10 each) : group I sham operation (group S) ; group II I/R and group III Isoflurane + I/R (group Iso). Myocardial I/R was induced by 40 min occlusion of left anterior descending branch (LAD) of coronary artery followed by 120 min reperfusion. In group III , 2% isoflurane in 100% 02 was inhaled for 2 h and I/R was produced 24 h later. At the end of 120 min reperfusion, arterial blood samples were taken for determination of serum SOD activity. The animals were then killed and hearts removed for determination of αB-crystallin expression and caspase-3 expression. Infarct size and area at risk were determined by Evan's blue and TFC staining. Myocardial ultrastructure was examined by electron microscopy. Results The infarct size was significantly smaller, serum SOD activity significantly higher, caspase-3 expression significantly lower, and αB-crystallin expression significantly higher in group Iso than in group I/R (P 〈 0.05). Microscopic examination showed less myocardial damage in group Iso than in group I/R. Conclusion The isoflurane-induced delayed preconditioning attenuates myocardial I/R injury possibly through up-regulating αB-crystallin expression in rabbits.
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2009年第9期825-827,共3页 Chinese Journal of Anesthesiology
基金 湖南省自然科学基金资助项目(03JJY3053) 湖南省科技厅资助项目(2007FJ3015)
关键词 晶体蛋白质类 异氟醚 缺血预处理 心肌 心肌再灌注损伤 Crystallins Isoflurane Ischemic preconditioning, myocardial Myocardial reperfusion injury
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参考文献11

  • 1Tanaka K, Ludwig LM, Krolikowski JG, et al. Isoflurane produces delayed preconditioning against myocardial ischemia and reperfusion injury: role of cyclooxygenase-2. Anesthesiology,2004,100:525-531.
  • 2Tonkovic-Capin M, Gross GJ, Bosnjak ZJ, et al. Delayed cardioprotection by isoflurane: role of KATP channels. Am J Physiol Heart Cire Physiol, 2002,283 : H61-H68.
  • 3Kato K, Shinohara H, Kurobe N, et al. Tissue distribution and developmental profiles of immunoreactive alpha B erystallin in the rat determined with a sensitive immunoassay system. Biochim Biophys Acta, 1991,1074 : 201-208.
  • 4肖卫民 黄勤 尢家马录 肖献忠.αB—晶状体蛋白在心肌预适应早期相及延迟相心肌保护中的作用[J].中国病理生理杂志,2000,16(10):968-968.
  • 5Morrison LE, Whittaker RJ, Klepper RE, et al. Roles for alphaB- crystallin and HSPB2 in protecting the myocardium from ischemiareperfusion-induced damage in a KO mouse model. Am J Physiol Heart Circ Physiol, 2004,286 : H847-H855.
  • 6Golenhofen N, Arbeiter A, Koob R, et al. Ischemia-indueed association of the stress protein alpha B-crystallin with I-band portion of cardiac titin. J Mol Cell Cardiol,2002,34:309-319.
  • 7Ray PS, Martin JL, Swanson EA, et al. Transgene overexpression of alphaB crystallin confers simultaneous protection against cardiomyocyte apoptosis and necrosis during myocardial ischemia and reperfusion. FASEB J, 2001,15 : 393-402.
  • 8Mehlen P, Kretz-Remy C, Preville X, et al. Human hsp27, Drosophila hsp27 and human alphaB-crystallin expression-mediated increase in glutathione is essential for the protective activity of these proteins against TNFalpha-induced cell death. EMBO J, 1996,15:2695-2706.
  • 9Takahashi A. Caspase: executioner and undertaker of apoptosis. Int J Hematol, 1999,70:226-232.
  • 10Wang X. The expanding role of mitochondria in apoptosis. Genes Dev, 2001,15 : 2922 -2933.

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同被引文献10

  • 1刘双,肖献忠.αB-晶体蛋白的功能与疾病[J].生命的化学,2005,25(2):89-91. 被引量:11
  • 2王尧玲,王建设,刘双,袁灿,吕青兰,刘梅冬,刘可,肖献忠.大鼠心肌缺血预适应延迟相的差异蛋白质的分离及鉴定[J].中国动脉硬化杂志,2005,13(4):456-460. 被引量:7
  • 3Dana A,Baxter GF,Yellon DM.Delayed or second windowpreconditioning induced by adenosine A1 receptor activation is independent of early generation of nitric oxide or late induction of inducible nitric oxide synthase.J Cardiovasc Pharmacol,2001,38:278-287.
  • 4Lasley RD,Keith BJ,Kristo G,et al.Delayed adenosine A1 receptor preconditioning in rat myocardium is MAPK dependent but iNOS independent.Am J Physiol Heart Circ Physiol,2005,289:785-791.
  • 5Xiao X,Benjamin IJ.Stress-response proteins in cardiovascular disease.Am J Hum Genet,1999,64:685-690.
  • 6Kregel KC.Heat shock proteins:modifying factors in physiological stress responses and acquired thermotolerance.J Appl Physio,2002,92:2177-2186.
  • 7Morrison LE,Hoover HE,Thuerauf DJ,et al.Mimicking phosphorylation of alpha B-crystallin on serine-59 is necessary and sufficient to provide maximal protection of cardiac myocytes from apoptosis.Circ Res,2003,92:203-211.
  • 8Ray PS,Martin JL,Swanson EA,et al.Transgene overexpression of alpha B-crystallin confers simultaneous protection against cardiomycyte apoptosis and necrosis during myocardial ischemia and reperfusion.FASEB J,2001,15:393-402.
  • 9Morrison LE,WhittakerRJ,Klepper RE,et al.Roles for alpha B-crystallin and HSPB2 in protecting the myocardium from ischemia-reperfusion-induced damage in a KO mouse model.Am J Physiol Heart Circ Physiol,2004,286:H847-H855.
  • 10吴镜湘,徐美英.腺苷心肌保护作用研究进展[J].中国心血管杂志,2002,7(5):364-366. 被引量:15

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