超过凝血酶原时间和活化的部分凝血活酶时间:体内凝血-一个说明审查。

IF 1
Neil S Harris, Maximo J Marin, Saulius Butenas
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引用次数: 0

摘要

体内启动凝血的步骤不同于凝血酶原时间(PT)和活化的部分凝血活素时间(aPTT)的组成部分。PT和aPTT的反应通过加入高浓度的组织因子(PT)或二氧化硅(aPTT)来保持分离。在体内,这些反应混合在一起作为起始阶段,然后是传播阶段。起始期产生少量凝血酶,而繁殖期产生大量凝血酶。当产生的凝血酶总量少于4%时,就会形成可见的凝块。虽然接触途径对aPTT反应至关重要,但这组反应在体内正常止血中不起作用,但在病理性血栓形成和炎症中似乎很重要。在体内,止血途径受抗凝血酶系统、组织因子途径抑制剂以及蛋白C和蛋白S复合物的控制。血小板和内皮细胞是止血的重要组成部分。在存在凝血酶和血管壁损伤的情况下,血小板被激活,它们粘附在出血部位并聚集,释放其他介质使血小板进一步聚集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beyond prothrombin time and activated partial thromboplastin time: coagulation in vivo-an illustrated review.

The steps that initiate coagulation in vivo are different from the components of prothrombin time (PT) and activated partial thromboplastin time (aPTT). The reactions of PT and aPTT are kept separate by the addition of high concentrations of tissue factor (for PT) or silica (for aPTT). In vivo, these reactions blend together as an initiation phase followed by a propagation phase. The initiation phase produces small quantities of thrombin, while much larger amounts of thrombin are generated by the propagation phase. Formation of a visible clot occurs when less than 4% of the total thrombin is generated. Although the contact pathway is essential for the aPTT reaction, this set of reactions does not play a role in normal hemostasis in vivo but does appear to be important in pathologic thrombosis and inflammation. The hemostatic pathways are controlled in vivo by the antithrombin system, tissue factor pathway inhibitor, and the protein C and protein S complexes. Platelets and endothelial cells are an essential component of hemostasis. In the presence of thrombin and vessel wall damage, platelets are activated, and they adhere to the bleeding site and aggregate releasing other mediators for further platelet aggregation.

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