Ockelford P A, Carter C J, Mitchell L, Hirsh J
Thromb Res. 1982 Nov 1;28(3):401-9. doi: 10.1016/0049-3848(82)90121-9.
The relationship between the in vivo antithrombotic effect of heparin and ex vivo anti-Xa activity has been investigated using an animal thrombosis model. Three low molecular weight heparins were compared with the standard heparin from which they were fractionated. All four heparins showed a dose-dependent antithrombotic effect enabling the relative antithrombotic and anti-Xa activities to be compared over a dosage range. A correlation between ex vivo anti-Xa heparin levels and antithrombotic effect was demonstrated for the standard (MW 16,000), intermediate (MW 7,600) and low (MW 4,600) molecular weight heparins but not for the ultra-low molecular weight (MW 3,000) fraction. The lack of relationship between anti-Xa activity and inhibition of thrombosis for the very low molecular weight fraction indicates that a very high anti-Xa activity (measured in vitro or ex vivo) is not always predictive of in vivo antithrombotic efficacy. These findings suggest that other properties of low molecular weight heparins contribute to their antithrombotic effectiveness.
利用动物血栓形成模型研究了肝素的体内抗血栓形成作用与体外抗Xa活性之间的关系。将三种低分子量肝素与从中分离出它们的标准肝素进行了比较。所有四种肝素均显示出剂量依赖性抗血栓形成作用,从而能够在一定剂量范围内比较相对抗血栓形成和抗Xa活性。对于标准(分子量16,000)、中等(分子量7,600)和低(分子量4,600)分子量肝素,证明了体外抗Xa肝素水平与抗血栓形成作用之间存在相关性,但对于超低分子量(分子量3,000)级分则未观察到这种相关性。极低分子量级分的抗Xa活性与血栓形成抑制之间缺乏相关性,这表明非常高的抗Xa活性(体外或体内测量)并不总是能够预测体内抗血栓形成疗效。这些发现表明,低分子量肝素的其他特性有助于其抗血栓形成效果。