Nakanishi E, Sato H, Nakajima A
J Biomed Mater Res. 1987 Feb;21(2):187-200. doi: 10.1002/jbm.820210204.
The inhibitory effect of heparin and antithrombin III (AT) on the interaction of fibrinogen and thrombin was investigated in preference to studies on heparinizing devices. The turbidity was measured kinetically as a measure of the concentration of fibrin polymer formed in the system. It was found that AT did not act on fibrinogen but, rather, on thrombin, and the main role of heparin is to accelerate the AT-thrombin reaction. On the other hand, dextran sulfate (DSc) did not accelerate the AT-thrombin reaction. When heparin and AT were incubated with thrombin, inhibition did not depend on the mixing order but on the incubation time. Thus, a ternary complex of heparin, AT, and thrombin was supposed to form for the inhibition. The reaction of heparin with fibrinogen and thrombin in the presence of AT was well-explained by assuming a Freundlich-type adsorption of heparin analogous with the reaction of heparin with fibrinogen.
相较于对肝素化装置的研究,我们更倾向于研究肝素和抗凝血酶III(AT)对纤维蛋白原与凝血酶相互作用的抑制作用。通过动力学方法测量浊度,以此作为系统中形成的纤维蛋白聚合物浓度的指标。结果发现,AT并非作用于纤维蛋白原,而是作用于凝血酶,并且肝素的主要作用是加速AT - 凝血酶反应。另一方面,硫酸葡聚糖(DSc)并未加速AT - 凝血酶反应。当肝素和AT与凝血酶一起孵育时,抑制作用并不取决于混合顺序,而是取决于孵育时间。因此,推测形成了肝素、AT和凝血酶的三元复合物以实现抑制作用。通过假定肝素的弗罗因德利希型吸附类似于肝素与纤维蛋白原的反应,很好地解释了在AT存在下肝素与纤维蛋白原和凝血酶的反应。