期刊文献+

克赛减轻不稳定型心绞痛患者血管内皮细胞损伤的研究

The study of Enoxaparin reducing the impairment of vascular endothelial cell of the unstable angina pectoris patients(UA)
暂未订购
导出
摘要 目的 探讨克赛引起的不稳定型心绞痛患者血浆血管性血友病因子 (v WF)与内皮素 (ET)的变化。方法 用酶联免疫吸附双抗体夹心法 (ELLSA)与放免法 (RIA)测定不稳定型心绞痛 30例 (1 5例应用克赛治疗 ,1 5例应用硝酸酯类、钙拮抗剂、β受体阻滞剂常规治疗 ) ,观察用药前及 1 w后 v WF、ET水平 ,并进行治疗前后及各组间的统计分析。结果 克赛组治疗前较常规治疗组明显升高 ,治疗后明显下降 ;治疗前克赛组与常规治疗组无显著差异 ,治疗后克赛组下降明显。结论 克赛能够降低不稳定型心绞痛患者血浆中的 v WF、ET水平 ,对血管内皮细胞有保护作用 ,能够减轻血管内皮细胞的损伤。 Objective To explore the change of vWF and ET caused by Enoxaparin of the UA patients. Methods To use Enzyme-Linked Immuno Sorbent Assay (ELLSA) and radioimmunoassay (RIA) to test thirty UA patients, among which fifteen for Enoxaparin group and the others using organic nitrates?calcium antagonists and β-adrenoceptor blocking drugs as the routine treating group. Then respectively do statistical analysis with the level of vWF and ET before treatment ?a week later and of twenty of the normal control group. Results before treatment, the level of the Enoxaparin group is obviously higher than that of the normal control group. After treatment, it is apparently coming down, the descent of which is more evident than the normal control group′s, even though the difference between the Enoxaparin group and the normal control group is little before treatment. Conclusions Enoxaparin is able to reduce the level of vWF and ET in the blood of the UA patients. It can protect vascular endotheliocyte and reduce the trauma.
出处 《中国老年学杂志》 CAS CSCD 北大核心 2003年第4期233-234,共2页 Chinese Journal of Gerontology
关键词 克赛 不稳定型心绞痛 血管内皮细胞损伤 血浆 血管性血友病因子 内皮素 Unstable angina pectoris Enoxaparin Von Willebrand factor Endothelin Endothelial cell
  • 相关文献

参考文献10

  • 1[1]Hirsh J,Leine MN.Low-molecular-weight heparin[J].Blood,1992;79:1-17.
  • 2[2]Melandri G, Semprini F, Cervi V, et al. Comparison of efficacy of low molecular weight heparin(parnaparin) with that of unfractionated heparin in the presence of activated platelets in healthy subjects[J]. Am J Cardiol, 1993; 72:450-454.
  • 3[3]Theroux P,Waters D,Lam J,et al.Reactivation of unstable angina after the discontinuation of heparin[J].N Engl J Med,1992;327-145.
  • 4[4]Samama MM,Bara L.Gerotziafas for the antithrombotic activity in man of low molecular weight heparins (LMWHs)[J].Haemostasis,1994;24:105-117.
  • 5[5]Montalescot G,Coller JP,Bison L,et al.Effects of variousanticoagulant treatments on von Willebrand factor release in unstable angina.J Am Coll Cardiol,2000;36(1):110-114.
  • 6[6]Montalescot G,Philippe F,Ankir A,et al.Early increase of vonWillebrand factor predicts adverse outcome in unstable coronary artery disease:beneficial[J].effects of enoxaparin,French Investigators of the ESSENNCE Trial [see comments].Circulation,1998;98(4):294-299.
  • 7[7]Vasile Visualization of the binding,endocytosis and transcytosis of low-density lipoprotein in the arterial endothelium in situ[J].J Cell Biol,1983;96:1677.
  • 8[8]Fromm JR,Hileman RE,Weiler JM,et al.Interaction of fibrobl-ast growth factor-l and relmed peptides with heparin sulfate and its oligosaccharide[J].Arch Biochem Biophys,1997; 15:346(2):252-262.
  • 9[9]Ross R.The pathogenesis of atherosclerosis:A perspective for the 1990s[J].Nature,1993;362:801.
  • 10[10]Griffith RL.LDL metabolism by macrophages activated with LDL immunocomplexes:A possible mechanism of foam cell formation[J].J Exp Med,1988;168:1041.

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