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精胺减轻大鼠在体心肌缺血/再灌注损伤的作用及机制初探 被引量:8

Effects of spermine on myocardial ischemia/ reperfusion injury in rats
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摘要 目的:观察低浓度外源性精胺对大鼠心肌缺血/再灌注损伤的影响。方法:Wistar大鼠随机分成假手术(Sham)组、缺血/再灌注损伤(I/R)组、盐水对照(NS)组和精胺干预(Sp)组(n=10)。结扎冠脉复制心肌缺血/再灌注损伤模型。Sp组缓慢静脉推注0.5mmol/L精胺2mL/kg。观察指标:心电图,心功能参数,血清SOD、LDH、NO、MDA水平和心肌超微结构等。结果:I/R组心律失常发生率高达90%,心肌超微结构损伤严重,LVSP和±dp/dtmax明显降低,血清中NO、MDA及LDH升高,SOD活性降低(P<0.05或P<0.01vsSham组)。Sp组与I/R组及NS组相比,上述指标均有显著差异(P<0.05或P<0.01)。结论:低浓度外源性精胺能减轻大鼠心肌缺血/再灌注损伤,其机制可能与抗氧化和减轻氧自由基损伤有关。 AIM: To observe the effect of exogenous spermine (low concentration) on myocardial ischemia/ reperfusion injury in rats. METHODS: 40 Wistar rats were randomly divided into 4 groups: sham - operation group (Sham), ischemic reperfusion group (I/R), spermine group (Sp) and natural saline group (NS). The model of ischemic/reperfusion injury was established by ligating rat coronary artery. In Sp group, spermine (0.5 mmol/L, 2 mL/kg) was injected slowly into rat vein. During the process, we recorded the electrocardiogram and the LV functional parameters, assayed the levels of SOD, LDH, NO and MDA in serum, and examined the ultrastructure of the myocardium. RESULTS: In I/R group, the incidence of arrhythmia was 90%, myocardial ultrastructure was injured seriously, values of LVSP and ± dp/dtmax decreased, levels of LDH, NO and MDA increased while SOD activity decreased ( P 〈 0. 05 or P 〈 0. 01, compared with Sham group). Compared with I/R and NS group, all those indexes in Sp group changed significantly ( P 〈 0.05 or P 〈 0.01 ). CONCLUSION : Exogenous spermine alleviates myocardial ischemia/reperfusion injury in rats. The mechanism may be related to its antioxidant effect and relieving the injury caused by oxygen free radical.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2007年第5期839-843,共5页 Chinese Journal of Pathophysiology
基金 国家自然科学基金资助项目(No.30370577 No.30470688) 黑龙江省教育厅海外学人科研(合作)资助项目(No.1053HQ010) 黑龙江省研究生创新科研资金资助项目
关键词 精胺 心肌再灌注损伤 活性氧 大鼠 Spermine Myocardial reperfusion injury Reactive oxygen species Rats
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参考文献13

  • 1王纪防,苏瑞斌,李锦.多胺与肿瘤发生发展及其在临床上的应用[J].国外医学(药学分册),2004,31(5):263-267. 被引量:7
  • 2Carmen B,Jose MR,Ana BV,et al.Increase in ornithine decarboxylase activity in the positive inotropism induced by androgens in isolated left atrium of the rat[J].Eur J Pharmacol,2001,422 (1 -2):101-107.
  • 3Addibhatla RM,James F,Hatcher KS,et al.Polyamines and central nervous system injury:spermine and spermidine decrease following transient focal cerebral ischemia in spontaneously hypertensive rats[J].Brain Res,2002,938(1 -2):81 -86.
  • 4徐长庆 赵雅君 孙亚南 等.多胺在心肌组织中的'双刃剑'样作用及其可能机制.中国病理生理杂志,2004,20(13):2384-2385.
  • 5Lin J,Bombeck CA,Yang S,et al.Nitric oxide suppresses apoptosis via interrupting caspase activation and mitochondrial dysfunction in cultured hepatocytes[J].J Biol Chem,1999,274 (24):17325-17333.
  • 6Das KC,Misra HP.Hydroxyl radical scavenging and singlet oxygen quenching properties of polyamines[J].Mol Cell Biochem,2004,262 (1 -2):127-133.
  • 7Marzabadi MR,Eric L.Spermine prevent iron accumulation and depress lipofuscin accumulation in cultured myocardial cells[J].Free Radic Biol Med,1996,21(3):375-381.
  • 8Commez M,Hellstrand.Endogenous polyamines modulate Ca^2+ channel activity in guinea-pig intestinal smooth muscle[J].Pflugers Arch Eur J Physiol,1999,438 (4):445-451.
  • 9Uehara A,Fill M,Velez P,et al.Rectification of rabbit cardiac ryanodine receptor current by endogenous polyamines[J].Biophys J,1996,71(2):769 -777.
  • 10Salvi M,Toninello A.Effects of polyamines on mitochondrial Ca^2+ transport[J].Biochim Biophys Acta,2004,1661(2):113 -124.

二级参考文献28

  • 1Kazuei I,Keiko K. Polyamines mysterious modulators of cellular function[J]. Jpn Biochem Biophy Res Commun,2000,271(3):559-564.
  • 2Anthony EP,Hiroshige H. Polyamine metabolism during cardiac hypertrophy[J]. Am J Physiol (Endocrinol. Metab.),1980,239(5):372-378.
  • 3Carmen B,Jose MR,Ana BV,et al. Increase in ornithine decarboxylase activity in the positive inotropism induced by androgens in isolated left atrium of the rat[J]. Eur J Pharmacol,2001,422(1-3):101-107.
  • 4Fermandez AI,Cantabrana B,Sanchez M,et al. Extracellular and intracellular effects of polyaminea on smooth muscle contraction[J]. Life Sci,1995,57(9):855-861.
  • 5Carlo V,Claudio F,Flavio F,et al. Polyamines effect on [Ca2+]i homeostasis and contractility in isolated rat ventricular cardiomyocytes[J]. Am J Physiol,1994,267(36):H587-H592.
  • 6Johnson TD,Childres WF,Bryan RM Jr. The in vitro action of polyamine on rat basilar and femoral artery contractile activity[J]. Life Sci,1996,59(7):529-536.
  • 7Shuuichi H,Masayuki N,Koei H,et al. Decrease in myocardial polyamine concentration in rats with myocardial infarction[J]. Life Sci,1997,60(19):1643-1650.
  • 8Nilisson BO,Gomez MF,Sward K,et al. Regulation of Ca2+ channel and phosphoatase activiyies by polyamines in intestinal and vascular smooth muscle-implications for cellular growth and contractility[J]. Acta Physiol Scand,2002,176:33-41.
  • 9Matkovics B,Kecskemeti V,Varga SI,et al. Antioxiddant properties of di-and polyamines[J]. Comp Biochem Physiol,1993,104B(3):475-479.
  • 10Hyo CHa,Nilantha SS,Periannan K,et al. The natural polyamine spermine functions directly as a free radical scavenger[J]. Proc Natl Acad Sci USA,1998,95(19):11140-11145.

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