Fischer A M, Merton R E, Marsh N A, Williams S, Gaffney P J, Barrowcliffe T W, Thomas D P
Thromb Haemost. 1982 Apr 30;47(2):109-13.
A comparison has been made between the effects of pentosan polysulphate (SP54) and mucosal heparin following subcutaneous injection in man. Unlike heparin, pentosan polysulphate has relatively little effect in vivo as measured by anti-factor Xa clotting assay and none by an anti-Xa amidolytic assay (S-2222). However, pentosan polysulphate is at least as potent as heparin on a weight basis in producing activation of lipoprotein lipase, shortening of the euglobulin clot lysis time and impairing the generation of factor Xa. Our data indicate that pentosan polysulphate has more marked effects in vivo than in vitro, that the action of the drug on clotting is mediated mainly via an At III-independent pathway, and that its effects are not confined to the coagulation system.
已对戊聚糖多硫酸酯(SP54)和黏膜肝素皮下注射给人后的效果进行了比较。与肝素不同,通过抗Xa凝血测定法测得戊聚糖多硫酸酯在体内的作用相对较小,而通过抗Xa酰胺分解测定法(S - 2222)则未检测到其作用效果。然而,按重量计算,戊聚糖多硫酸酯在激活脂蛋白脂肪酶、缩短优球蛋白凝块溶解时间以及抑制Xa因子生成方面至少与肝素一样有效。我们的数据表明,戊聚糖多硫酸酯在体内的作用比在体外更显著,该药物对凝血的作用主要通过不依赖抗凝血酶III(At III)的途径介导,并且其作用不限于凝血系统。