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特异性抗体、D-苯丙氨酰-脯氨酰-精氨酸-氯甲基酮和抑肽酶对重组组织型纤溶酶原激活剂体外止血参数影响的预防作用比较

Comparison of specific antibody, D-Phe-Pro-Arg-CH2Cl and aprotinin for prevention of in vitro effects of recombinant tissue-type plasminogen activator on haemostasis parameters.

作者信息

Seifried E, Tanswell P

机构信息

Abteilung Innere Medizin III, Universität Ulm, FRG.

出版信息

Thromb Haemost. 1987 Oct 28;58(3):921-6.

PMID:2448890
Abstract

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.

摘要

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。

相似文献

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引用本文的文献

1
Inhibition of desmoteplase-induced fibrinolytic activity in vitro.体外抑制去氨普酶诱导的纤溶活性。
J Thromb Thrombolysis. 2005 Aug;20(1):23-6. doi: 10.1007/s11239-005-2465-4.
2
Pharmacokinetics and pharmacodynamics of tenecteplase in fibrinolytic therapy of acute myocardial infarction.替奈普酶在急性心肌梗死溶栓治疗中的药代动力学和药效学
Clin Pharmacokinet. 2002;41(15):1229-45. doi: 10.2165/00003088-200241150-00001.
3
Plasma resistance to activated protein C regulates the activation of coagulation induced by thrombolysis in patients with ischaemic heart disease.
血浆对活化蛋白C的抵抗作用调节缺血性心脏病患者溶栓诱导的凝血激活。
Heart. 1997 Feb;77(2):122-7. doi: 10.1136/hrt.77.2.122.
4
Prospective randomized clinical study in general surgery comparing a new low molecular weight heparin with unfractionated heparin in the prevention of thrombosis.普通外科领域的前瞻性随机临床研究:比较一种新型低分子量肝素与普通肝素在预防血栓形成方面的效果。
Clin Investig. 1994 Nov;72(11):913-9. doi: 10.1007/BF00190751.
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Tissue-type plasminogen activator. A review of its pharmacology and therapeutic use as a thrombolytic agent.组织型纤溶酶原激活剂。其药理学及作为溶栓剂的治疗用途综述。
Drugs. 1989 Sep;38(3):346-88. doi: 10.2165/00003495-198938030-00003.