Notohamiprodjo M, Andrassy K, Bommer J, Ritz E
Blood Purif. 1986;4(1-3):130-41. doi: 10.1159/000169436.
Artificial membranes used for hemodialysis differ from endogenous membranes, i.e. endothelial cells, by their variable thrombogenicity. The key step in activation of the coagulation system by dialysis membranes is thrombocyte activation which is preceded by formation of a protein layer of critical thickness. Crucial questions concerning the quality of this protein membrane as a determinant of thrombocyte activation are not well understood. Activation of the contact phase of the intrinsic plasmatic coagulation system by dialysis membranes is well documented. Local action of thrombin in the membrane microenvironment is documented by release of fibrinopeptide A and deposition of fibrin on the membrane. Apart from thrombin, other mechanisms, e.g. PMN elastase, plasma-independent activation of blood cells, facilitatory action of erythrocytes etc., may play a contributory role. With respect to the polycarbonate membrane, some authors find less platelet extraction and unchanged platelet release reaction. In our own studies, polycarbonate membranes were not superior to cuprophane membranes with respect to thrombogenicity.
用于血液透析的人工膜与内源性膜(即内皮细胞)的不同之处在于其血栓形成倾向各异。透析膜激活凝血系统的关键步骤是血小板激活,而这之前会形成一层临界厚度的蛋白质层。关于这种蛋白质膜作为血小板激活决定因素的质量的关键问题尚未得到充分理解。透析膜激活内源性血浆凝血系统接触相已得到充分证实。膜微环境中凝血酶的局部作用可通过纤维蛋白肽A的释放和纤维蛋白在膜上的沉积得以证明。除凝血酶外,其他机制,如PMN弹性蛋白酶、血细胞的血浆非依赖性激活、红细胞的促进作用等,可能也起到一定作用。对于聚碳酸酯膜,一些作者发现其血小板提取较少且血小板释放反应不变。在我们自己的研究中,聚碳酸酯膜在血栓形成倾向方面并不优于铜仿膜。