Poon M C, Hurst R E, Rives M S
Thromb Haemost. 1982 Apr 30;47(2):162-5.
The role of heparin structure in neutralization by the neutralizing substances (NS) platelet factor 4 (PF4) and protamine sulfate (PS) was investigated using a thrombin clotting assay and a series of more homogeneous heparin fractions varying systematically in charge density (Z). For a given heparin, plotting inverse clotting times measured without NS, and in the presence of PF4 or PS, vs heparin concentration yielded approximately parallel straight lines displaced horizontally according to the amount of NS. Potencies of heparin fractions in the absence of NS, or in the presence of PF4 of PS, depended almost identically upon Z2. Small but significant quantitative differences in potency among equivalent fractions from different heparins showed both PF4 and PS had a slight preference for the least active subfraction of decolorized heparins, but for the most active subfraction of undecolorized heparins. Neutralization of heparin by PF4 and PS probably proceeds by similar mechanisms, but the details of structure outside the antithrombin III-binding oligosaccharide of heparin may enter in differently.
利用凝血酶凝血试验以及一系列电荷密度(Z)呈系统性变化的更均匀的肝素级分,研究了肝素结构在被中和物质(NS)、血小板因子4(PF4)和硫酸鱼精蛋白(PS)中和过程中的作用。对于给定的肝素,绘制在无NS、存在PF4或PS的情况下测得的凝血时间倒数与肝素浓度的关系图,得到大致平行的直线,这些直线根据NS的量在水平方向上发生位移。在无NS或存在PF4或PS的情况下,肝素级分的效力几乎同样取决于Z²。来自不同肝素的等效级分在效力上存在微小但显著的定量差异,这表明PF4和PS都略微倾向于脱色肝素中活性最低的亚级分,但倾向于未脱色肝素中活性最高的亚级分。PF4和PS对肝素的中和作用可能通过相似的机制进行,但肝素抗凝血酶III结合寡糖之外的结构细节可能以不同方式参与其中。