期刊文献+

异丙酚对大鼠离体心脏缺血/再灌注损伤时心肌c-fos基因表达的影响 被引量:1

The effect of propofol on c-fos gene expression during global myocardial ischemia-reperfusion in isolated rat heart
下载PDF
导出
摘要 目的观察异丙酚对离体大鼠全心缺血再灌注损伤心肌c-fos基因表达的影响,探讨其对缺血再灌注损伤心肌保护作用机制。方法Wistar大鼠36只,随机分为对照组和异丙酚组,每组又分为缺血前、缺血30min和复灌30min3个亚组。通过离体心肌灌注模型,采用免疫组化及RT-PCR观察心肌c-fos蛋白及c-fosmRNA表达水平的变化。结果与缺血前相比,缺血30min及再灌注30min亚组的c-fos蛋白的光密度值及c-fosmRNA表达水平均增加(P<0.01);与对照组相比,异丙酚各亚组的c-fos蛋白光密度值及c-fosmRNA表达水平均降低(P<0.01)。结论c-fos基因参与了心肌缺血再灌注损伤的基因调节。异丙酚可减轻心肌c-fos基因的表达,并可避免或减轻心肌缺血再灌注损伤。 Objective To study the protective effects of propofol on isolated rat heart during global myocardial ischemia-reperfusion. Methods 36 Wistar rats were randomly divided into control group and propofol group. Each group was subdivided into 3 subgroups: preiscbemia, ischemia 30 minutes and ischemia-reperfusion 30 minutes group. The changes in c-fos protein and c-fos mRNA level in isolated Langendorff perfused rat myocardium were assessed by immunohistochemical technique and RT-PCR technique respectively. Resdts Compared to preischemia subgroup the expression of c-fos protein and c-fos mRNA level in ischemia 30 minutes and ischemia-reperfusion 30 minutes subgroups were higher significantly (P〈0. 01). As compared with the values of control group, the expression of c-fos protein and c-fos mRNA level were lowered in propofol group of iscbemia 30 minutes and reperfusion 30 minutes (P〈0. 01). Condusion c-fos gene may be involved in molecular modulation of myocardial ischemia-reperfusion injury. Propofol can depress the expression of c-fos gene in myocardium, thus contribute to ameliorate and obviate the myocardial ischemia-reperfusion injury.
出处 《解放军医学杂志》 CAS CSCD 北大核心 2006年第5期440-441,共2页 Medical Journal of Chinese People's Liberation Army
基金 全军青年基金资助项目(01Q005)
关键词 心肌缺血 再灌注损伤 基因 fos myocardial ischemia reperfusion injury gene, fos
  • 相关文献

参考文献5

  • 1Brand T,Sharma HS,Fleischmann KE et al.Proto-oncogene expression in porcine myocardium sudjected to ischemia and reperfusion.Cir Res,1992,71(6):1351.
  • 2Wechsler AS,Entwistle JW,Ding M et al.Myocardial stunning association with altered gene expression.J Card Surg,1994,9(3suppl):537.
  • 3Plumier JC,Robertson HA,Currie RW.Differential accumulation of mRNA for immediate early genes and heat shock genes in heart after ischemic injury.J Mol Cell Cardiol,1996,28(6):1251.
  • 4Hall RI,Murphy JT,Landymore R et al.Myocardial metabolic and hemodynamic changes during propofol anesthesia for cardiac surgery in patents with reduced ventricular function.Anesth Analg,1993,77(4):680.
  • 5孙莹杰,高光洁,张铁铮,宋丹丹,刘晓江.异丙酚对大鼠肝脏缺氧复氧损伤的保护作用[J].解放军医学杂志,2005,30(1):64-65. 被引量:5

二级参考文献7

  • 1Basu S, Nozari A, Liu XL et al. Development of a novel biomarker offree radical damage in reperfusion injury after cardiac arrest. FEBS Lett,2000,47(1) :1.
  • 2Zwart L, Meerman J, Commandeur J,et al.Biomarkers of free radical damage: applications in experimental animals and in humans. Free Radic Biol Med, 1999,26(1-2):202.
  • 3Pratico D. F2-isoprostanes: sensitive and specific non-invasive indices of lipid peroxidation in vivo. Atheroslerosis, 1999, 147( 1 ) : 1.
  • 4Morrow JD, Awad JA, Kato T etal. Formation of novel non- cyclooxygenase- derived prostanoids (F2 - isoprostanes) in carbon tetrachloride hepatotoxicity. An animal model of lipid peroxidation. J Clin Invest,1992,90(6) : 2502.
  • 5Awad JA,Burk RF, Roberts Id. Effect of selenium deficiency and glutathione-modulating agents on diquat toxicity and lipid peroxidation in rats.J Pharmacol Exp Ther , 1994, 270(3);858.
  • 6Ma TT, Ischiropoulos H, Brass CA. Endotoxin stimulated nitric oxide production increases injury and reduces rat liver ehemilumineseene during reperfusion. Gastroenterology, 1995,108(2) :463.
  • 7Fukabori M, Ichimori K, Ishida H et al. Nitric oxide reversible suppress xanthine oxidase activity. Free Radical Res, 1994,21(4) :203.

共引文献4

同被引文献29

引证文献1

二级引证文献3

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