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1型纤溶酶原激活物抑制剂对缺血性心脏病患者组织型纤溶酶原激活物介导的纤维蛋白溶解的调节作用:利尿剂可能产生的不利影响。

Regulation of tissue-type plasminogen activator-mediated fibrinolysis by plasminogen activator inhibitor type-1 in patients with ischaemic heart disease: possible unfavourable effect of diuretics.

作者信息

Pedersen O D, Gram J, Bagger H, Keller N, Jespersen J

机构信息

Departments of Clinical Chemistry, Ribe County Hospital, Esbjerg, Denmark.

出版信息

Coron Artery Dis. 1994 Jul;5(7):617-23. doi: 10.1097/00019501-199407000-00010.

Abstract

BACKGROUND

Impaired endogenous tissue-type plasminogen activator (t-PA)-mediated fibrinolysis may be involved in the evolution of myocardial infarction. t-PA-mediated fibrinolysis is believed to depend on the amount of active t-PA present in the circulation. Accordingly, we investigated the possible mechanisms responsible for impaired t-PA-mediated fibrinolysis in patients with ischaemic heart disease.

METHODS

Forty-five survivors of acute myocardial infarction were examined 8 weeks after discharge from hospital. Intravenous infusion of 1-desamino-8-D-arginine vasopressin (DDAVP; 0.4 micrograms/kg bodyweight) was used to stimulate the endogenous fibrinolytic system, and blood samples were collected before and after infusion. We compared the response of the t-PA-plasminogen activator inhibitor type-1 (PAI-1) fibrinolytic system in patients with preinfusion levels of active t-PA below or at the detection limit of the assay with that in patients with higher preinfusion levels of active t-PA.

RESULTS

All patients responded to DDAVP infusion with an increase in plasma concentration of t-PA antigen. This response did not differ between the two groups. In contrast, the preinfusion levels of PAI activity were significantly higher in patients with undetectable plasma levels of active t-PA compared with patients with higher levels of active t-PA (22.3 versus 12.8 IU/ml; P < 0.01). Subgroup analyses demonstrated that patients treated with diuretics had significantly higher plasma concentrations of PAI-1 antigen (28.5 versus 17.9 ng/ml; P < 0.03) and a trend towards higher PAI activity (24.0 versus 14.6 IU/ml; P = 0.07) compared with patients not receiving diuretics.

CONCLUSION

Our study strongly suggests that a high plasma level of PAI-1, the main inhibitor of t-PA, is responsible for impaired t-PA-mediated fibrinolysis in patients with ischaemic heart disease, and that treatment with diuretics may be associated with an unfavourable effect on the fibrinolytic system.

摘要

背景

内源性组织型纤溶酶原激活物(t-PA)介导的纤维蛋白溶解功能受损可能参与心肌梗死的发展过程。t-PA介导的纤维蛋白溶解被认为取决于循环中活性t-PA的量。因此,我们研究了缺血性心脏病患者t-PA介导的纤维蛋白溶解功能受损的可能机制。

方法

45例急性心肌梗死幸存者在出院8周后接受检查。静脉输注1-去氨基-8-D-精氨酸加压素(DDAVP;0.4微克/千克体重)以刺激内源性纤维蛋白溶解系统,并在输注前后采集血样。我们比较了输注前活性t-PA水平低于或处于检测限的患者与输注前活性t-PA水平较高的患者的t-PA-纤溶酶原激活物抑制剂1型(PAI-1)纤维蛋白溶解系统的反应。

结果

所有患者对DDAVP输注的反应都是血浆t-PA抗原浓度升高。两组之间的这种反应没有差异。相比之下,活性t-PA血浆水平不可检测的患者的输注前PAI活性水平明显高于活性t-PA水平较高的患者(22.3对12.8 IU/ml;P<0.01)。亚组分析表明,与未接受利尿剂治疗的患者相比,接受利尿剂治疗的患者血浆PAI-1抗原浓度明显更高(28.5对17.9 ng/ml;P<0.03),并且PAI活性有升高趋势(24.0对14.6 IU/ml;P=0.07)。

结论

我们的研究强烈表明,t-PA的主要抑制剂PAI-1的高血浆水平是缺血性心脏病患者t-PA介导的纤维蛋白溶解功能受损的原因,并且利尿剂治疗可能对纤维蛋白溶解系统产生不利影响。

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