Béguin S, Lindhout T, Hemker H C
Department of Biochemistry, University of Limburg, Maastricht, The Netherlands.
Thromb Haemost. 1988 Dec 22;60(3):457-62.
The influence of heparin on prothrombin conversion in plasma was estimated by measuring prothrombin disappearance with the aid of staphylocoagulase or by calculation from the thrombin generation curve, compensating for simultaneous thrombin inactivation by plasma protease inhibitors. In thromboplastin-activated plasma the effect of heparin on prothrombinase (factor Xa-factor Va-phospholipid) is negligible compared to that on thrombin probably because both the extrinsic factor X activating complex and phospholipid bound factor Xa are insensitive to AT III-heparin action. In contact-activated plasma prothrombinase generation is inhibited by heparin, because heparin lowers the ambient concentrations of thrombin so that the feedback activation of factor VIII by thrombin is diminished. Consequently, the delayed factor Xa generation causes a lag phase in prothrombinase generation. We conclude that heparin in plasma acts by its thrombin scavenging properties. No direct action on prothrombinase or on the factor X activating enzyme needs to be assumed if one takes into account the effect of thrombin depletion on thrombin-mediated feedback reactions.
通过使用葡萄球菌凝固酶测量凝血酶原消失情况,或根据凝血酶生成曲线进行计算,并补偿血浆蛋白酶抑制剂同时导致的凝血酶失活,来评估肝素对血浆中凝血酶原转化的影响。在组织凝血活酶激活的血浆中,与肝素对凝血酶的作用相比,其对凝血酶原酶(因子Xa - 因子Va - 磷脂)的影响可忽略不计,这可能是因为外源性因子X激活复合物和磷脂结合的因子Xa均对抗凝血酶III - 肝素作用不敏感。在接触激活的血浆中,凝血酶原酶的生成受到肝素抑制,因为肝素降低了凝血酶的周围浓度,从而使凝血酶对因子VIII的反馈激活减弱。因此,因子Xa生成延迟导致凝血酶原酶生成出现滞后阶段。我们得出结论,血浆中的肝素通过其清除凝血酶的特性发挥作用。如果考虑到凝血酶消耗对凝血酶介导的反馈反应的影响,则无需假定肝素对凝血酶原酶或因子X激活酶有直接作用。