Ts'ao C, Gardner D V, Galluzzo T S, Molteni A
Arch Int Pharmacodyn Ther. 1984 Jan;267(1):169-76.
The effect of captopril, MK-421 and MK-422 on fibrinolysis was investigated in vitro with 3 assay methods. Incorporation of captopril, but not MK-421 and MK-422, into fibrin clots resulted in a reduction of fibrinolysis by purified human plasmin. The concentrations of captopril required to demonstrate this effect far exceeded the therapeutic doses. Pre-mixing plasmin with captopril did not lead to a decreased lysis of fibrin plates. Furthermore, none of these agents affected the lysis of 125I-fibrin plates by a mixture of human serum and streptokinase. Captopril and MK-421, and to a much lesser extent MK-422, inhibited the amidolysis of a fluorogenic synthetic substrate by human plasmin; the inhibition was ameliorated by increasing the substrate concentration. Apparently, the inhibition of fibrinolysis by high doses of captopril, and of amidolysis by captopril and MK-421, appears to lie in their effects on the substrate (fibrin and synthetic substrate) rather than on the enzyme (plasmin).
采用3种检测方法在体外研究了卡托普利、MK-421和MK-422对纤维蛋白溶解的影响。将卡托普利而非MK-421和MK-422掺入纤维蛋白凝块中会导致纯化的人纤溶酶引起的纤维蛋白溶解减少。证明这种作用所需的卡托普利浓度远远超过治疗剂量。将纤溶酶与卡托普利预混合不会导致纤维蛋白平板的溶解减少。此外,这些药物均未影响人血清和链激酶混合物对125I标记的纤维蛋白平板的溶解。卡托普利和MK-421,以及在小得多的程度上MK-422,抑制人纤溶酶对荧光合成底物的酰胺水解;通过增加底物浓度可改善这种抑制作用。显然,高剂量卡托普利对纤维蛋白溶解的抑制作用,以及卡托普利和MK-421对酰胺水解的抑制作用,似乎在于它们对底物(纤维蛋白和合成底物)而非对酶(纤溶酶)的影响。