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低分子量肝素在兔体内的出血与抗血栓形成特性之间的关系。

The relationship between the hemorrhagic and antithrombotic properties of low molecular weight heparin in rabbits.

作者信息

Carter C J, Kelton J G, Hirsh J, Cerskus A, Santos A V, Gent M

出版信息

Blood. 1982 Jun;59(6):1239-45.

PMID:7082826
Abstract

We have compared the hemorrhagic and antithrombotic effects of a low molecular weight (LMW) heparin fraction and standard heparin in rabbits. Similar LMW heparin fractions have antithrombotic effects when tested in animals, but their hemorrhagic effects relative to standard heparin have not been established. Standard porcine mucosal heparin (mol wt 15,000 daltons) was depolymerized by nitrous acid to a low molecular weight fraction (mol wt 4600 daltons). Using equal USP units, the standard and Dep LMW heparin were compared in vitro, ex vivo, and in vivo. In vitro, when diluted in rabbit plasma, the Dep LMW heparin at equivalent anti-Xa activity showed less prolongation of thrombin clotting times or activated partial thromboplastin times. Ex vivo, platelets from rabbits treated with the Dep LMW heparin showed less inhibition of collagen-induced aggregation. The relative hemorrhagic properties of the two heparins were compared in vivo in rabbits using a sensitive blood loss assay, and the antithrombotic properties were compared in a thrombin-induced venous stasis model. By using an optimal threshold heparin dose in each test system, it was possible to demonstrate that equal USP units of Dep LMW heparin caused less blood loss but showed greater antithrombotic activity than standard heparin.

摘要

我们比较了低分子量(LMW)肝素组分和标准肝素对家兔的出血及抗血栓形成作用。类似的低分子量肝素组分在动物实验中具有抗血栓形成作用,但其相对于标准肝素的出血作用尚未明确。标准猪黏膜肝素(分子量15,000道尔顿)经亚硝酸解聚成低分子量组分(分子量4600道尔顿)。使用相等的美国药典单位,对标准肝素和去聚低分子量肝素进行了体外、离体及体内比较。在体外,当在兔血浆中稀释时,具有等效抗Xa活性的去聚低分子量肝素对凝血酶凝结时间或活化部分凝血活酶时间的延长作用较小。在离体实验中,用去聚低分子量肝素处理的家兔血小板对胶原诱导的聚集抑制作用较小。使用敏感的失血测定法在体内比较了两种肝素的相对出血特性,并在凝血酶诱导的静脉淤滞模型中比较了它们的抗血栓形成特性。通过在每个测试系统中使用最佳阈值肝素剂量,得以证明相等美国药典单位的去聚低分子量肝素导致的失血量较少,但比标准肝素具有更强的抗血栓形成活性。

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