Stief Thomas W
Department of Clinical Chemistry-Central Laboratory, University Hospital, Marburg, Germany.
Clin Appl Thromb Hemost. 2007 Apr;13(2):146-53. doi: 10.1177/1076029606298987.
The inhibition of plasmatic thrombin is of clinical importance in a broad range of diseases. To obtain reliable data the assay system should be as similar to physiology as possible. Using a newly developed physiologic assay system for fibrinogen/thrombin interaction (the FIFTA), the inhibition of plasmatic thrombin by heparin or by arginine was studied. The standard fibrinogen functional turbidimetric assay (FIFTA) was performed, varying heparin or arginine concentrations and varying the time point the inhibitor was added to the FIFTA. Plasmatic heparin concentrations equal to or greater than 0.63 IU/mL completely inhibit thrombin in the assay system described. The IC(50) is 0.1 IU/mL heparin. Heparin can only inhibit fibrin generation within the first 2 minutes at room temperature (RT=23 degrees C). The 50% inhibitory time point, that is, the time point that a 10 IU/mL final concentration of heparin results in 50% inhibition of FIFTA, is 30 seconds at RT. A final arginine concentration of at least 125 mM in the first 100 seconds of the FIFTA reaction at RT completely inhibits turbidity increase. Half-maximal turbidity increase occurs at 63 mM arginine. Final arginine concentrations of at least 250 mM completely inhibit turbidity increase, when arginine acts in the first 4 minutes (RT) of the thrombin/ fibrinogen interaction. A final arginine concentration of 477 mM added at the 12-minute or 30-minute thrombin/ fibrinogen reaction time point decreases the resulting turbidity by 50% after an additional 30 minutes at RT. Pathologic disseminated intravascular coagulation occurs in a multitude of diseases; in common is always the generation of thrombin either by the contact phase or by the tissue factor phase of coagulation. Such pathologically elevated thrombin activity in blood or blood products must be prevented or inhibited. This study demonstrates the efficiency of two physiologic thrombin inhibitors: heparin and arginine.
血浆凝血酶的抑制作用在多种疾病中具有临床重要性。为了获得可靠的数据,检测系统应尽可能与生理状态相似。使用新开发的用于纤维蛋白原/凝血酶相互作用的生理检测系统(FIFTA),研究了肝素或精氨酸对血浆凝血酶的抑制作用。进行了标准纤维蛋白原功能比浊法检测(FIFTA),改变肝素或精氨酸的浓度,并改变抑制剂添加到FIFTA中的时间点。在所描述的检测系统中,血浆肝素浓度等于或大于0.63 IU/mL可完全抑制凝血酶。IC(50)为0.1 IU/mL肝素。肝素仅在室温(RT = 23摄氏度)下的前2分钟内抑制纤维蛋白生成。50%抑制时间点,即最终浓度为10 IU/mL的肝素导致FIFTA抑制50%的时间点,在室温下为30秒。在室温下FIFTA反应的前100秒内,最终精氨酸浓度至少为125 mM可完全抑制浊度增加。半最大浊度增加发生在63 mM精氨酸时。当精氨酸在凝血酶/纤维蛋白原相互作用的前4分钟(室温)起作用时,最终精氨酸浓度至少为250 mM可完全抑制浊度增加。在凝血酶/纤维蛋白原反应时间点为12分钟或30分钟时添加最终浓度为477 mM的精氨酸,在室温下再过30分钟后可使产生的浊度降低50%。病理性弥散性血管内凝血发生在多种疾病中;共同之处总是通过凝血的接触相或组织因子相产生凝血酶。必须预防或抑制血液或血液制品中这种病理性升高的凝血酶活性。本研究证明了两种生理性凝血酶抑制剂:肝素和精氨酸的有效性。