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低分子量肝素对实验性血栓形成和止血的影响——生产方法的影响

The effect of low molecular weight heparin on experimental thrombosis and haemostasis--the influence of production method.

作者信息

Ostergaard P B, Nilsson B, Bergqvist D, Hedner U, Pedersen P C

出版信息

Thromb Res. 1987 Mar 15;45(6):739-49. doi: 10.1016/0049-3848(87)90084-3.

Abstract

Three low molecular weight heparins prepared by enzymatic depolymerization, chemical degradation, and fractionation, respectively were studied in experimental thrombosis and haemostasis models in vivo and in biological assays in vitro. The three low molecular weight heparins, which had comparable molecular weight distributions, showed very similar activities both in vitro and in vivo. All three showed dose dependent thromboprophylactic effect. The antithrombotic effects of the low molecular weight heparins and conventional heparin administered in the same dose (30 XaI u/kg b.w.) did not differ. Neither LMW heparin nor conventional heparin (60 or 90 XaI u/kg b.w.) showed significant effects on the haemostatic plug formation time in the rabbit mesenteric microcirculation. These experiments confirm that low molecular weight heparins are potential antithrombotic drugs, which by intravenous administration have effects similar to those of standard heparin. The method of preparation seems to be of no or minor importance, at least if the molecular weight distributions of the products are similar.

摘要

分别通过酶解聚、化学降解和分级分离制备的三种低分子量肝素,在体内实验性血栓形成和止血模型以及体外生物学测定中进行了研究。这三种低分子量肝素具有相当的分子量分布,在体外和体内均表现出非常相似的活性。所有三种都显示出剂量依赖性的血栓预防作用。相同剂量(30 XaI单位/千克体重)的低分子量肝素和传统肝素的抗血栓作用没有差异。低分子量肝素和传统肝素(60或90 XaI单位/千克体重)对兔肠系膜微循环中止血栓形成时间均无显著影响。这些实验证实,低分子量肝素是潜在的抗血栓药物,静脉给药时其作用与标准肝素相似。制备方法似乎无关紧要或重要性较小,至少如果产品的分子量分布相似的话。

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