Zacharski L R, Rosenstein R
Blood. 1979 Mar;53(3):366-74.
The coagulant of normal human saliva has been identified as tissue factor (thromboplastin, TF) by virtue of its ability to cause rapid coagulation in plasmas deficient in first-stage coagulation factors and to activate factor x in the presence of factor VII and by virtue of the fact that its activity is expressed only in the presence of factor VII and is inhibited by an antibody to TF. The TF is related to cells and cell fragments in saliva. Salivary TF activity has been found to be significantly reduced in patients taking warfarin. The decline in TF activity during induction of warfarin anticoagulation occurs during the warfarin-induced decline in vitamin-K-dependent clotting factor activity, as judged by the prothrombin time. The decrease in TF activity is not related to a reduction in salivary cell count or total protein content or to a direct effect of warfarin on the assay. It is hypothesized that the mechanism by which warfarin inhibits TF activity may be related to the mechanism by which it inhibits expression of the activity of the vitamin-K-dependent clotting factors. Inhibition of the TF activity may be involved in the antithrombotic effect of warfarin.
正常人唾液中的凝血剂已被鉴定为组织因子(凝血活酶,TF),这是由于它能够在缺乏一级凝血因子的血浆中引起快速凝血,并在因子VII存在的情况下激活因子X,还因为其活性仅在因子VII存在时才表现出来,且会被TF抗体抑制。TF与唾液中的细胞及细胞碎片有关。已发现服用华法林的患者唾液TF活性显著降低。根据凝血酶原时间判断,在华法林诱导抗凝过程中,TF活性的下降发生在华法林诱导的维生素K依赖性凝血因子活性下降期间。TF活性的降低与唾液细胞计数或总蛋白含量的减少无关,也与华法林对检测的直接影响无关。据推测,华法林抑制TF活性的机制可能与其抑制维生素K依赖性凝血因子活性表达的机制有关。TF活性的抑制可能参与了华法林的抗血栓形成作用。