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溶栓药物在体内的协同作用。

Synergism of thrombolytic agents in vivo.

作者信息

Collen D, Stassen J M, Stump D C, Verstraete M

出版信息

Circulation. 1986 Oct;74(4):838-42. doi: 10.1161/01.cir.74.4.838.

DOI:10.1161/01.cir.74.4.838
PMID:3093116
Abstract

The existence of significant synergism between tissue-type plasminogen activator (t-PA) and single-chain urokinase-type plasminogen activator (scu-PA), and between t-PA and urokinase in thrombolysis in vivo is described. In a quantitative preparation of thrombolysis, consisting of rabbits in which a blood clot was induced in the jugular vein with 125I-labeled fibrin, intravenous infusion over 4 hr of t-PA, scu-PA, or urokinase in amounts of 0.5, 1.0, or 2.0 mg/kg body weight resulted in significant thrombolysis (30% to 60%). The simultaneous infusion of t-PA and scu-PA or of t-PA and urokinase had a significantly greater (p less than .001) thrombolytic effect than could be anticipated on the basis of the added effects of each agents alone. However, no synergism was observed between scu-PA and urokinase. The observed alpha 2-antiplasmin consumption and fibrinogen breakdown after urokinase at higher doses did not occur with the equivalent thrombolytic combinations of t-PA and urokinase. The combined use of synergic thrombolytic agents in patients may permit a significant reduction in total administered doses, probably with elimination of the systemic activation of the fibrinolytic system and the concomitant fibrinogen breakdown that is unavoidable with the currently used thrombolytic doses of each agent.

摘要

本文描述了组织型纤溶酶原激活剂(t-PA)与单链尿激酶型纤溶酶原激活剂(scu-PA)之间,以及t-PA与尿激酶在体内溶栓过程中存在显著协同作用。在一项定量溶栓实验中,以家兔为实验对象,通过向颈静脉注射125I标记的纤维蛋白诱导形成血栓,然后分别静脉输注剂量为0.5、1.0或2.0mg/kg体重的t-PA、scu-PA或尿激酶,持续4小时,结果显示有显著的溶栓效果(30%至60%)。同时输注t-PA和scu-PA或t-PA和尿激酶,其溶栓效果比单独使用每种药物的叠加效应预期的要显著得多(p<0.001)。然而,未观察到scu-PA和尿激酶之间存在协同作用。高剂量尿激酶后观察到的α2-抗纤溶酶消耗和纤维蛋白原降解,在t-PA和尿激酶等效溶栓组合中并未出现。在患者中联合使用协同溶栓剂可能会显著减少总给药剂量,可能避免纤维蛋白溶解系统的全身激活以及目前使用的每种药物溶栓剂量时不可避免的伴随纤维蛋白原降解。

相似文献

1
Synergism of thrombolytic agents in vivo.溶栓药物在体内的协同作用。
Circulation. 1986 Oct;74(4):838-42. doi: 10.1161/01.cir.74.4.838.
2
Synergistic effect on thrombolysis of sequential infusion of tissue-type plasminogen activator (t-PA) single-chain urokinase-type plasminogen activator (scu-PA) and urokinase in the rabbit jugular vein thrombosis model.组织型纤溶酶原激活剂(t-PA)、单链尿激酶型纤溶酶原激活剂(scu-PA)和尿激酶序贯输注对兔颈静脉血栓形成模型溶栓的协同作用。
Thromb Haemost. 1987 Oct 28;58(3):943-6.
3
Absence of synergism between tissue-type plasminogen activator (t-PA), single-chain urokinase-type plasminogen activator (scu-PA) and urokinase on clot lysis in a plasma milieu in vitro.组织型纤溶酶原激活剂(t-PA)、单链尿激酶型纤溶酶原激活剂(scu-PA)和尿激酶在体外血浆环境中对血凝块溶解不存在协同作用。
Thromb Haemost. 1986 Aug 20;56(1):35-9.
4
Comparative thrombolytic properties of bolus injections and continuous infusions of a chimeric (t-PA/u-PA) plasminogen activator in a hamster pulmonary embolism model.在仓鼠肺栓塞模型中推注注射与持续输注嵌合型(组织型纤溶酶原激活剂/尿激酶型纤溶酶原激活剂)纤溶酶原激活剂的溶栓特性比较。
Blood. 1991 Jul 1;78(1):125-31.
5
Comparative thrombolytic properties of single-chain forms of urokinase-type plasminogen activator.
Blood. 1987 Feb;69(2):592-6.
6
Thrombolytic and pharmacokinetic properties of chimeric tissue-type and urokinase-type plasminogen activators.嵌合组织型和尿激酶型纤溶酶原激活剂的溶栓及药代动力学特性
Circulation. 1991 Sep;84(3):1216-34. doi: 10.1161/01.cir.84.3.1216.
7
Comparative thrombolytic properties of tissue-type plasminogen activator (t-PA), single-chain urokinase-type plasminogen activator (u-PA) and K1K2Pu (a t-PA/u-PA chimera) in a combined arterial and venous thrombosis model in the dog.在犬动静脉联合血栓形成模型中组织型纤溶酶原激活剂(t-PA)、单链尿激酶型纤溶酶原激活剂(u-PA)和K1K2Pu(一种t-PA/u-PA嵌合体)的溶栓特性比较
J Am Coll Cardiol. 1992 May;19(6):1350-9. doi: 10.1016/0735-1097(92)90344-m.
8
Thrombolytic and pharmacokinetic properties of a recombinant chimeric plasminogen activator consisting of a fibrin fragment D-dimer specific humanized monoclonal antibody and a truncated single-chain urokinase.一种由纤维蛋白片段D - 二聚体特异性人源化单克隆抗体和截短的单链尿激酶组成的重组嵌合纤溶酶原激活剂的溶栓和药代动力学特性
Thromb Haemost. 1992 Aug 3;68(2):170-9.
9
Molecular mechanism of action of newer thrombolytic agents.新型溶栓药物的分子作用机制
J Am Coll Cardiol. 1987 Nov;10(5 Suppl B):11B-15B. doi: 10.1016/s0735-1097(87)80422-9.
10
Thrombolytic therapy.溶栓治疗
Annu Rev Med. 1988;39:405-23. doi: 10.1146/annurev.me.39.020188.002201.

引用本文的文献

1
Is thrombolysis alone the best therapy for acute myocardial infarction? Current status and emerging strategies.单纯溶栓是急性心肌梗死的最佳治疗方法吗?现状与新策略
Tex Heart Inst J. 1991;18(1):50-61.
2
Thrombolytics: drug interactions of clinical significance.溶栓剂:具有临床意义的药物相互作用。
Drug Saf. 2000 Nov;23(5):391-9. doi: 10.2165/00002018-200023050-00004.
3
Drug interactions with thrombolytic agents. Current perspectives.与溶栓药物的药物相互作用。当前观点
Clin Pharmacokinet. 1995 Apr;28(4):315-26. doi: 10.2165/00003088-199528040-00004.
4
New strategies in the development of thrombolytic agents.溶栓药物开发的新策略。
Blut. 1988 Oct;57(4):147-62. doi: 10.1007/BF00319543.
5
Complementary modes of action of tissue-type plasminogen activator and pro-urokinase by which their synergistic effect on clot lysis may be explained.组织型纤溶酶原激活剂和尿激酶原的互补作用模式,据此可解释它们对血栓溶解的协同效应。
J Clin Invest. 1988 Mar;81(3):853-9. doi: 10.1172/JCI113394.
6
Thrombolysis in the management of acute myocardial infarction and unstable angina pectoris.溶栓疗法在急性心肌梗死和不稳定型心绞痛治疗中的应用
Drugs. 1989 Feb;37(2):191-204. doi: 10.2165/00003495-198937020-00006.
7
Thrombolysis. An approach still on the move.溶栓治疗:一种仍在不断发展的方法。
Drugs. 1989 Feb;37(2):116-22. doi: 10.2165/00003495-198937020-00002.
8
Use of plasminogen activators in venous thrombosis.
World J Surg. 1990 Sep-Oct;14(5):688-93. doi: 10.1007/BF01658826.
9
Intra-arterial thrombolysis should be the initial treatment of the acutely ischaemic lower limb.动脉内溶栓应作为急性下肢缺血的初始治疗方法。
Ann R Coll Surg Engl. 1992 Mar;74(2):106-10; discussion 111.
10
Advances in thrombolytic therapy.溶栓治疗的进展。
Cardiovasc Drugs Ther. 1992 Apr;6(2):111-24. doi: 10.1007/BF00054557.