Mode of action of enoxaparin in plasma.

S Béguin, H C Hemker
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Abstract

Unfractionated heparin in the extrinsic system has an action on prothrombinase that is insignificant compared to its antithrombin action. In the intrinsic system, unfractionated heparin does have an indirect antiprothrombinase action because its antithrombin activity inhibits the feedback activation of Factor VIII. Most low molecular weight heparins are not different from unfractionated heparin, although their antiprothrombinase action may be slightly higher. Among these, enoxaparin has the highest antiprothrombinase action, due to a relatively high content of very low molecular weight material. In platelet rich plasma, there is an important difference between unfractionated and low molecular weight heparin in that, up to 0.3 U/ml, unfractionated heparin is completely neutralized by activated platelets (300,000 microliters/l) whereas low molecular weight heparins are not. Therefore, unfractionated heparin in platelet rich plasma acts only on the lag phase of thrombin production and not on the amount of thrombin produced. Low molecular weight heparins significantly prolong the lag time and inhibit the thrombin peak in platelet rich plasma.

依诺肝素在血浆中的作用方式。
外源系统中未分离的肝素对凝血酶原的作用与其抗凝血酶作用相比微不足道。在内在系统中,未分离肝素确实具有间接抗凝血酶原作用,因为其抗凝血酶活性抑制因子VIII的反馈激活。大多数低分子量肝素与未分离肝素没有什么不同,尽管它们的抗凝血酶原作用可能略高。其中,依诺肝素具有最高的抗凝血酶原作用,这是由于其含有相对较高的极低分子量物质。在富含血小板的血浆中,未分离的肝素和低分子量肝素之间有一个重要的区别,在0.3 U/ml时,未分离的肝素可以被活化的血小板完全中和(300,000微升/l),而低分子量肝素则不能。因此,富血小板血浆中未分离的肝素仅作用于凝血酶产生的滞后期,而不作用于凝血酶产生的量。低分子量肝素显著延长了血小板富集血浆中凝血酶的滞后时间并抑制了凝血酶峰值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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