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组织因子途径抑制物是否参与肝素的抗血栓形成作用?生化方面的考量。

Is tissue factor pathway inhibitor involved in the antithrombotic effect of heparins? Biochemical considerations.

作者信息

Ostergaard P, Nordfang O, Petersen L C, Valentin S, Kristensen H

机构信息

Heparin Research Laboratory, Biopharmaceuticals Research, Novo Nordisk A/S, Gentofte, Denmark.

出版信息

Haemostasis. 1993 Mar;23 Suppl 1:107-11. doi: 10.1159/000216919.

Abstract

Tissue factor pathway inhibitor (TFPI) is released into the circulation after intravenous or subcutaneous injection of heparin or low-molecular-weight heparin (Logiparin) in humans. The plasma concentration of TFPI is increased 2- to 4-fold by a prophylactic dose of Logiparin, and this excess TFPI remains in the circulation only in the presence of the heparin. TFPI and heparin show strong synergism in clotting assays at concentrations obtained after heparin injection in humans. Animal studies have demonstrated that TFPI by itself has antithrombotic properties. It is concluded that the release of TFPI may contribute significantly to the antithrombotic effect of heparin.

摘要

在人类静脉注射或皮下注射肝素或低分子量肝素(洛吉派林)后,组织因子途径抑制物(TFPI)会释放到循环系统中。预防性剂量的洛吉派林可使TFPI的血浆浓度升高2至4倍,并且只有在肝素存在的情况下,这种过量的TFPI才会留在循环系统中。在人类注射肝素后所达到的浓度下,TFPI与肝素在凝血试验中表现出强烈的协同作用。动物研究表明,TFPI本身具有抗血栓形成特性。由此得出结论,TFPI的释放可能对肝素的抗血栓形成作用有显著贡献。

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