Seifried E, Tanswell P
Abteilung Innere Medizin III, Universität Ulm, FRG.
Thromb Haemost. 1987 Oct 28;58(3):921-6.
In vitro, concentration-dependent effects of rt-PA on a range of coagulation and fibrinolytic assays in thawed plasma samples were investigated. In absence of a fibrinolytic inhibitor, 2 micrograms rt-PA/ml blood (3.4 micrograms/ml plasma) caused prolongation of clotting time assays and decreases of plasminogen (to 44% of the control value), fibrinogen (to 27%), alpha 2-antiplasmin (to less than 5%), FV (to 67%), FVIII (to 41%) and FXIII (to 16%). Of three inhibitors tested, a specific polyclonal anti-rt-PA antibody prevented interferences in all fibrinolytic and most clotting assays. D-Phe-Pro-Arg-CH2Cl (PPACK) enabled correct assays of fibrinogen and fibrinolytic parameters but interfered with coagulometric assays dependent on endogenous thrombin generation. Aprotinin was suitable only for a restricted range of both assay types. Most in vitro effects were observed only with rt-PA plasma concentrations in excess of therapeutic values. Nevertheless it is concluded that for clinical application, collection of blood samples on either specific antibody or PPACK is essential for a correct assessment of in vivo effects of rt-PA on the haemostatic system in patients undergoing fibrinolytic therapy.
在体外,研究了重组组织型纤溶酶原激活剂(rt-PA)对解冻血浆样本中一系列凝血和纤维蛋白溶解试验的浓度依赖性影响。在没有纤维蛋白溶解抑制剂的情况下,2微克rt-PA/毫升血液(3.4微克/毫升血浆)导致凝血时间试验延长,纤溶酶原(降至对照值的44%)、纤维蛋白原(降至27%)、α2-抗纤溶酶(降至5%以下)、FV(降至67%)、FVIII(降至41%)和FXIII(降至16%)减少。在测试的三种抑制剂中,一种特异性多克隆抗rt-PA抗体可防止所有纤维蛋白溶解试验和大多数凝血试验受到干扰。D-苯丙氨酸-脯氨酸-精氨酸-氯甲基酮(PPACK)能正确测定纤维蛋白原和纤维蛋白溶解参数,但会干扰依赖内源性凝血酶生成的凝血测定。抑肽酶仅适用于这两种试验类型的有限范围。大多数体外效应仅在rt-PA血浆浓度超过治疗值时才观察到。然而,得出的结论是,对于临床应用,采集使用特异性抗体或PPACK的血样对于正确评估rt-PA对接受纤维蛋白溶解治疗患者止血系统的体内效应至关重要。