Jensen O H, Slot O, Ernst E
Department of Rheumatology, Aalborg Sygehus Nord, Denmark.
Curr Med Res Opin. 1989;11(8):518-22. doi: 10.1185/03007998909110463.
The effect of 20 mg tenoxicam once daily for 7 days on various components of the fibrinolytic system was studied in 10 healthy volunteers. Plasma plasminogen, antithrombin 3, and prekallikrein decreased significantly while plasma plasminogen activator inhibitor increased significantly. The medication did not affect fibrin plate lysis area or the plasma level of plasminogen activator, alpha-2-antiplasmin, alpha-2-macroglobulin, C1 inactivator or Factor XII. It is suggested that these changes may be caused by interference with hepatic enzyme systems. The reduction in plasma prekallikrein may indicate that tenoxicam exerts its anti-inflammatory effect by more than one mechanism.
在10名健康志愿者中研究了每日一次服用20毫克替诺昔康,连续服用7天对纤维蛋白溶解系统各组分的影响。血浆纤溶酶原、抗凝血酶3和前激肽释放酶显著降低,而血浆纤溶酶原激活物抑制剂显著增加。该药物不影响纤维蛋白平板溶解面积或血浆纤溶酶原激活物、α2-抗纤溶酶、α2-巨球蛋白、C1灭活剂或因子XII的水平。提示这些变化可能是由于对肝酶系统的干扰所致。血浆前激肽释放酶的降低可能表明替诺昔康通过多种机制发挥其抗炎作用。