Gallimore M J, Tyler H M, Shaw J T
J Clin Pathol. 1972 Mar;25(3):185-90. doi: 10.1136/jcp.25.3.185.
It has been shown that the incubation of human plasma with urokinase at a concentration sufficient to cause rapid lysis of the clots formed on the addition of thrombin does not give rise to the production of measurable concentrations of non-clottable fibrinogen breakdown products. Also, breakdown products could not be detected in the course of experiments in vivo when urokinase was administered to monkeys and only in very low concentrations when a fibrinolytic state was induced by exercise in three healthy human volunteers. In contrast, high concentrations of breakdown products were found after thrombin infusion into monkeys. It is concluded that circulating fibrinogen is not readily broken down into non-clottable products by the fibrinolytic enzymes, and that normal animals and healthy human subjects do not have substantial deposits of fibrin that are available for breakdown during a fibrinolytic episode. The presence of breakdown products in the circulation is therefore likely to be indicative of the fibrinolytic response to an initial coagulation event.
已经表明,用人血浆与尿激酶在足以导致加入凝血酶后形成的凝块迅速溶解的浓度下孵育,不会产生可测量浓度的不可凝纤维蛋白原降解产物。此外,当给猴子施用尿激酶时,在体内实验过程中未检测到降解产物,而在三名健康人类志愿者中通过运动诱导纤维蛋白溶解状态时,仅以非常低的浓度检测到降解产物。相比之下,向猴子输注凝血酶后发现了高浓度的降解产物。结论是,循环中的纤维蛋白原不容易被纤维蛋白溶解酶分解成不可凝产物,并且正常动物和健康人类受试者在纤维蛋白溶解发作期间没有大量可用于分解的纤维蛋白沉积物。因此,循环中降解产物的存在可能表明对初始凝血事件的纤维蛋白溶解反应。