首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Anticoagulant synergism of heparin and activated protein C in vitro. Role of a novel anticoagulant mechanism of heparin enhancement of inactivation of factor V by activated protein C.
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Anticoagulant synergism of heparin and activated protein C in vitro. Role of a novel anticoagulant mechanism of heparin enhancement of inactivation of factor V by activated protein C.

机译:肝素和活化蛋白C在体外的抗凝协同作用。肝素的新型抗凝机制的作用增强活化蛋白C对因子V的灭活作用。

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摘要

Interactions between standard heparin and the physiological anticoagulant plasma protein, activated protein C (APC) were studied. The ability of heparin to prolong the activated partial thromboplastin time and the factor Xa- one-stage clotting time of normal plasma was markedly enhanced by addition of purified APC to the assays. Experiments using purified clotting factors showed that heparin enhanced by fourfold the phospholipid-dependent inactivation of factor V by APC. In contrast to factor V, there was no effect of heparin on inactivation of thrombin-activated factor Va by APC. Based on SDS-PAGE analysis, heparin enhanced the rate of proteolysis of factor V but not factor Va by APC. Coagulation assays using immunodepleted plasmas showed that the enhancement of heparin action by APC was independent of antithrombin III, heparin cofactor II, and protein S. Experiments using purified proteins showed that heparin did not inhibit factor V activation by thrombin. In summary, heparin and APC showed significant anticoagulant synergy in plasma due to three mechanisms that simultaneously decreased thrombin generation by the prothrombinase complex. These mechanisms include: first, heparin enhancement of antithrombin III-dependent inhibition of factor V activation by thrombin; second, the inactivation of membrane-bound FVa by APC; and third, the proteolytic inactivation of membrane-bound factor V by APC, which is enhanced by heparin.
机译:研究了标准肝素与生理抗凝血浆蛋白,活化蛋白C(APC)之间的相互作用。通过向测定中添加纯化的APC,肝素延长正常血浆部分凝血活酶时间和Xa因子一阶段凝血时间的能力显着增强。使用纯化的凝血因子的实验表明,肝素通过APC使因子V的磷脂依赖失活增加了四倍。与因子V相反,肝素对APC对凝血酶激活因子Va的灭活没有作用。基于SDS-PAGE分析,肝素通过APC增强了因子V而不是因子Va的蛋白水解速率。使用免疫耗竭血浆进行的凝集测定表明,APC对肝素作用的增强独立于抗凝血酶III,肝素辅因子II和蛋白S。使用纯化蛋白进行的实验表明,肝素不抑制凝血酶对V因子的激活。总之,由于三种机制同时降低了凝血酶原酶复合物的凝血酶生成,肝素和APC在血浆中显示出显着的抗凝协同作用。这些机制包括:首先,肝素增强抗凝血酶III依赖性凝血酶对因子V激活的抑制作用;第二,APC使膜结合的FVa失活。第三,肝素增强了APC对膜结合因子V的蛋白水解失活。

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