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CY216和CY222在血浆中的作用模式。

The mode of action of CY216 and CY222 in plasma.

作者信息

Béguin S, Wielders S, Lormeau J C, Hemker H C

机构信息

Department of Biochemistry, University of Limburg, Maastricht, The Netherlands.

出版信息

Thromb Haemost. 1992 Jan 23;67(1):33-41.

PMID:1319616
Abstract

Three fractions of the low molecular weight heparin CY216 (fraxiparin, mean molecular weight [MMW] 5,090), with MMWs of respectively, 3,090, 4,400 and 7,910 were prepared by gel permeation chromatography. From CY222 (MMW 3,770) as well as from CY216 and its three fractions the material with high affinity to antithrombin III (AT III) was obtained by chromatography on immobilised AT III. The molecular weight distribution of each of the ten preparations thus obtained was determined by high performance liquid chromatography, while the content of AT III binding material was determined by stoichiometric titration of AT III, monitored by intrinsic fluorescence enhancement. We measured the effect of all heparins on the decay of endogenous thrombin in plasma and on the overall generation of thrombin in plasma, triggered via the extrinsic or via the intrinsic pathway. From these data we calculated the time course of prothrombin conversion, i.e. the course of factor Xa activity as expressed by prothrombinase activity. It was found that in platelet-poor plasma the anticoagulant properties of the heparins are largely dependent on their antithrombin action, which is determined by their content of high affinity material with a MW of 5,400 or higher. The specific antithrombin activity of all heparins, when expressed in terms of material with high affinity to antithrombin III (HAM) with a MW greater than 5,400 is 13.0 min-1/(microgram/ml) (range 10.5-15.9).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过凝胶渗透色谱法制备了低分子量肝素CY216(速避凝,平均分子量[MMW]5090)的三个级分,其分子量分别为3090、4400和7910。从CY222(MMW 3770)以及CY216及其三个级分中,通过固定化抗凝血酶III柱色谱法获得了与抗凝血酶III(AT III)具有高亲和力的物质。通过高效液相色谱法测定由此获得的十种制剂中每一种的分子量分布,同时通过内在荧光增强监测的AT III化学计量滴定法测定AT III结合物质的含量。我们测量了所有肝素对血浆中内源性凝血酶衰减以及通过外源性或内源性途径触发的血浆中凝血酶总生成的影响。根据这些数据,我们计算了凝血酶原转化的时间进程,即由凝血酶原酶活性表示的因子Xa活性进程。发现在少血小板血浆中,肝素的抗凝特性在很大程度上取决于其抗凝血酶作用,这由其分子量为5400或更高的高亲和力物质的含量决定。当以分子量大于5400的与抗凝血酶III具有高亲和力的物质(HAM)表示时,所有肝素的比抗凝血酶活性为13.0 min-1/(微克/毫升)(范围10.5 - 15.9)。

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