Shuman M A, Levine S P
J Clin Invest. 1980 Feb;65(2):307-13. doi: 10.1172/JCI109673.
We have studied the effects of both impaired prothrombin activation and direct inhibition of thrombin on the platelet release reaction in clotting blood to determine the role of thrombin in this process. In blood from two patients with congenital Factor V deficiency, prothrombin activation during spontaneous in vitro clotting was delayed and decreased. Secretion of platelet Factor 4 was also delayed and was detected only after thrombin formation was initiated. Addition of a small amount of normal plasma to the patients' blood in vitro corrected the abnormalities in both thrombin formation and the platelet release reaction in parallel fashion. A delay in the onset of secretion of platelet Factor 4 was also observed when thrombin generated in normal blood during spontaneous in vitro clotting was inhibited by either purified hirudin or anti-thrombin Fab. These observations suggest that thrombin is the essential stimulus for platelet secretion during in vitro blood clotting. The effect of inhibitors of the platelet release reaction on prothrombin activation during in vitro blood clotting was also studied. When either prostacyclin or the combination of prostaglandin E(1) and N(6)O(2')-dibutyryl cyclic AMP was added, secretion of platelet Factor 4 was inhibited 85-95%. We were unable to detect any inhibition of initiation of prothrombin activation or inhibition of that part of thrombin generation associated with clotting. These results indicate either that the platelet release reaction may not be required for the initiation of prothrombin activation or only a very limited amount of secretion may be necessary for normal generation of thrombin to occur.
我们研究了凝血酶原激活受损和凝血酶直接抑制对凝血血液中血小板释放反应的影响,以确定凝血酶在此过程中的作用。在两名先天性因子V缺乏症患者的血液中,体外自发凝血过程中凝血酶原激活延迟且减少。血小板因子4的分泌也延迟,且仅在凝血酶形成开始后才检测到。在体外向患者血液中添加少量正常血浆,可同时纠正凝血酶形成和血小板释放反应的异常。当体外自发凝血过程中正常血液中产生的凝血酶被纯化的水蛭素或抗凝血酶Fab抑制时,也观察到血小板因子4分泌开始延迟。这些观察结果表明,凝血酶是体外血液凝固过程中血小板分泌的必要刺激因素。我们还研究了血小板释放反应抑制剂对体外血液凝固过程中凝血酶原激活的影响。当添加前列环素或前列腺素E(1)与N(6)O(2')-二丁酰环磷酸腺苷的组合时,血小板因子4的分泌被抑制85-95%。我们未能检测到凝血酶原激活起始的任何抑制或与凝血相关的凝血酶生成部分的抑制。这些结果表明,要么凝血酶原激活起始可能不需要血小板释放反应,要么正常凝血酶生成可能仅需要非常有限量的分泌。