期刊文献+

腺苷与AMP579对冠心病患者中性粒细胞表面CD11b/CD18表达的影响

The effect of adenosine to the expression of adhesion molecules CD11b/CD18 in patients with coronary heart disease
下载PDF
导出
摘要 目的:探讨不同剂量腺苷与AMP579对不同类型冠心病(CHD)患者中性粒细胞表面CD11b/CD18表达的影响。方法:选择经临床症状、心电图改变及心肌酶学确诊的CHD患者及正常健康者采血,患者血液分别给予不同剂量的腺苷与AMP579进行干预,免疫荧光标记后用流式细胞仪分别检测正常人及患者用药前后中性粒细胞CD11b/CD18的表达值。结果:CHD患者的中性粒细胞CD11b/CD18的表达较正常人明显升高(P<0.01);腺苷在10,30,100μmol能有效降低CHD患者的中性粒细胞CD11b/CD18的表达(P<0.05),但30,100μmol组之间差异无显著性(P>0.05);AMP579组中,患者中性粒细胞CD11b/CD18的表达均未见明显降低,各组较对照组差异均无统计学意义(P>0.05)。结论:CHD的发生与CD11b/CD18表达升高有关;腺苷可通过降低CD11b/CD18的表达而降低白细胞与内皮细胞之间的黏附性;而AMP579在1,10,30μmol尚不能降低CHD患者CD11b/CD18的表达。 Objective :To explore the effect of the different doses AMP579 and adenosine to the expression of adhesion molecules CD11b/CD18 on neutrophils in different types of patients with coronary heart disease(CHD). Methods :The patients and normal healthy individuals were drew blood ,patients blood were given different doses of adenosine and AMP579 to interval,the expression of CD11b/CD18 on neutrophils of normal people and patient were measured by direct immunofluorescence techniques associated with flow cytomerey. Results :Expression of CD11b/CD18 on neutrophils in the CHD patients were markedly higher than those in normal cases (P〈0. 01). Adenosine can reduced expression of CD11 b/CD18 in CHD patients on neutrophils in 10,30, 100 μmol (P 〈 0. 05 ), but expression of CDllb/CD18 in 30 μmol and in 100 μmol were no significantly different(P〈0.05). In AMP579 groups,the expression of CD11b/CD18 in CHD patients on neutrophils were no decreased significantly,there were no statistical significant (P〈0. 05). Conclusion :The incidence of coronary heart disease related with the increasing of CD11b/CD18 expression,adenosine can reduce CD11b/CD18 expression to reduce the adhesion of white blood cell and endothelial cell. AMP579 can't reduce the expression of CD11b/CD18 on neutrophils of CHD patients in 1,10,30 μmol.
作者 田继华 王雄
出处 《临床医药实践》 2008年第6期405-408,共4页 Proceeding of Clinical Medicine
关键词 冠心病 中性粒细胞 CD11B/CD18 腺苷 AMP579 coronary heart disease neutrophils CDllb/CD18 adenosine AMP579
  • 相关文献

参考文献9

  • 1Pasceri V,Willerson J T,Yeh E T.Modulation of Creactive protein mediated monocyte chemoattractant protein 1 induction in human endothelial cells by anti-atheroselerosis drug[J].Circulation,2001,103:2531-2534.
  • 2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
  • 3Budde J M,Velez O A,Zhao Z,et al.Comparative study of AMP579 and adenosine in inhibition of neutrophil-mediated vascular and myocardial injury during 24 h of reperfusion[J].Cardiovase Res,2000,47(2):294-305.
  • 4Xu Z,Yang X M,Cohem M V,et al.Limitation of infarct size in rabbit hearts by the novel adenosine receptor agonist AMP 579 administered at reperfusion[J].Mol Cell Cardiol,2000,32:2339-2347.
  • 5Oe K,Sperlagh B,Santha E,et al.Modulation of norepinephrine release by ATP-dependent K+-channel activators and inhibitors in guinea-pig and human isolated right atrium[J].Cardiovasc Res,1999,43:125-134.
  • 6Xu Z,Downey G M,Cohen M V.AMP 579 reduces contracture and limits infarction in rabbit heart by activating adenosine A 2 receptors[J].Cardiovasc Pharmacol,2001,38(3):474-481.
  • 7Nakamura M,Zhao Z Q,Clark K L,et al.A novel adenosine analog,AMP579,inhibits neutrophil activation,adherence and neutrophil-mediated injury to coronary vascular endothelium[J].Pharmacol,2000,397(1):197-205.
  • 8Zhao Z Q,Nakamura M,Wang N P,et al.Administration of adenosine during reperfusion reduces injury of vascular endothelium and death of myocytes[J].Coron Artery Dis,1999,10:617-628.
  • 9Kopecky S L,Aviles R J,Bell M R,et al.A randomized,double-blinded,placebo-controlled,dose-ranging study measuring percutaneous transluminal coronary angioplasty:the ADMIRE(AMP579 delivery for myocardial infarction reduction)study[J].American Heart Journal,2003,146(1):146-152.

二级参考文献24

  • 1Martynyuk AE, Kane KA, Cobbe SM, et al. Nitric oxide mediates the anti-adrenergic effect of adenosine on calcium current in isolated rabbit atrioventricular nodal cells. Pflugers Arch,1996,431:452-457.
  • 2Henry P, Demolombe S, Puceat M, et al. Adenosine At stimulation activates protein kinase C in rat ventrieular myocytes.Cire Res, 1996,78 : 161-165.
  • 3Oe K, Sperlagh B, Santha E, et al. Modulation of norepinephrine release by ATP-dependent K^+-channel activators and inhibitors in guinea-pig and human isolated right atrium.Cardiovasc Res, 1999,43 : 125-134.
  • 4Duan D, Ye L, Britton F, et al. Purinocepter-coupled Cl-channels in mouse heart :a novel, alternative pathway for CFTR regulation. Physiology(Lond), 1999,521 (pt 1):43-56.
  • 5Baxter GF, Yellon DM. Time course of delayed myocardial protection after transient adenosine A1-recepter activation in therabbit. J Cardiovasc Pharmacol, 1997,29 : 631-638.
  • 6Dreseher S, Bosch RF, Mewis C. et al. Administration of adenosine for termination of atrioventrieular nodal reentry taehyeardia: induction of atrial fibrillation with rapid conduction over an accessory pathway and unmasking of concomitant Wolff-Parkinson-White syndrome. Z Kardiol, 2000, 89: 522-526.
  • 7Paul T,Pfammatter JP. Adenosine: an effective and safe antiarrhythmic drug in pediatrics. Pediatr Cardiol, 1997,18:118-126.
  • 8Lee HT, LaFaro R J, Reed GE. Pretreatment of human myoeardium with adenosine during open heart surgery. J Card Surg, 1995,10:665-676.
  • 9McCully JD, Uematsu M, Parker RA, et al. Adenosine-enhanced isehemie preconditioning provides enhanced eardioproteetion in the aged heart. Ann Thorae Surg, 1998, 66: 2037-2043.
  • 10Mehta AB, Mardikar HM, Hiregouder NS, et al. Preconditioning the human myocardium with intracoronary adenosine. Indian Heart J,1998,50:397-401.

共引文献14

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