流式细胞术检测阿司匹林对冠心病患者血小板活化标志物的影响  被引量:9

Effect of aspirin on platelet activation markers in patients with coronary heart disease by FCM

在线阅读下载全文

作  者:张文超[1] 韦建瑞[1] 蒋作锋[1] 黎庆梅[1] 张锐[1] 郭壮波[1] 

机构地区:[1]暨南大学第四附属医院广州市红十字会医院,广东广州510220

出  处:《中国医院药学杂志》2007年第2期164-167,共4页Chinese Journal of Hospital Pharmacy

基  金:2005年广东省科技厅基金(编号:53064);2004年广州市医药卫生科技重点项目资助(编号:2004Z006)

摘  要:目的:探讨冠心病患者及其服用阿司匹林前后血小板表面糖蛋白的变化及其意义。方法:采用流式细胞仪(flow cy-tometry,FCM)测定冠心病患者阿司匹林治疗前后的全血中血小板表面糖蛋白(CD62p/PAC-1)的表达率,采用自身对照分析阿司匹林对血小板表面糖蛋白的影响。结果:冠心病组治疗前的血小板表面糖蛋白PAC-1、CD62p的表达率分别为(10.4±6.2)%和(10.7±7.1)%,较健康对照组明显升高(P<0.01),经以阿司匹林为基础的抗血小板治疗后CD62p、PAC-1的表达率下降至(4.3±2.1)%和(4.9±2.4)%(P<0.01),但仍高于健康对照组。结论:CD62p和PAC-1是血小板活化的敏感和特异指标,阿司匹林能够抑制血小板表面糖蛋白的表达,从而抑制血小板活化,抑制血栓形成。OBJECTIVE To explore the changes of platelet activation glycoprotein before and after treatment and the clinical significance in the patients with coronary heart diseases. METHODS CD62p,PAC-1 from whole blood samples were measured by FCM in 22 normal people and 38 patients with CHD before and after treatment. RESULTS Before treatment the percentage of CD62p positive and PAC-1 positive platelet were ( 10. 4 ± 6. 2)% and ( 10. 7 ± 7. 1 )%, respectively, and were significantly higher than those of normal control(P〈0.0l ). After treatment the percentage of CD62p positive and PAC-1 positive platelet were (4. 3 ± 2. 1 )% and (4. 9 ± 2. 4)% respectively and were declined evidently than those before treatment (P〈0.01 ), but still higher than those of normal control (P〈0.01 ). CONCLUSION Platelet activation plays an important role in the pathogenesis of coronary heart diseases. CD62p and PAC 1 is the sensitive index of platelet activation. Aspirin can inhibit the express of platelet activation glycoprotein. The detection of platelet function by FCM can be used for the evaluation of thromboembolic disease.

关 键 词:冠心病 CD62P PAC-1 流式细胞仪 

分 类 号:R971[医药卫生—药品]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象