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一种藻类硫酸化半乳聚糖对静脉血栓形成具有不同寻常的双重作用,这是由于它激活了因子XII并抑制了凝血蛋白酶。

An algal sulfated galactan has an unusual dual effect on venous thrombosis due to activation of factor XII and inhibition of the coagulation proteases.

作者信息

Melo Fábio R, Mourão Paulo A S

机构信息

Laboratório de Tecido Conjuntivo, Hospital Universitário Clementino Fraga Filho and Programa de Glicobiologia, Instituto de Bioquímica Médica, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Thromb Haemost. 2008 Mar;99(3):531-8. doi: 10.1160/TH07-10-0649.

DOI:10.1160/TH07-10-0649
PMID:18327401
Abstract

Sulfated galactan from the red alga Botryocladia occidentalis has a potent anticoagulant activity, due to its ability to enhance thrombin and factor Xa inhibition by antithrombin and/or heparin cofactor II. It is less active than unfractionated heparin in arterial thrombosis, but in a venous thrombosis presents a dual effect, inhibiting thrombosis in low but not in high doses. This dual effect on venous thrombosis is a consequence of two actions, one that inhibits thrombin and factor Xa and one that induces factor XII activation. In order to dissociate these effects, we prepared derivatives of the sulfated galactan with low molecular weights. Two fractions that were similar in size to unfractionated heparin and low-molecular-weight heparin were obtained. As the molecular weight decreased, the ability to activate factor XII and to promote inhibition of coagulation proteases in the presence of antithrombin and heparin cofactor II diminished. At approximately 5 kDa, the sulfated galactan fragment had no effect on factor XII activation, and showed the same effect as unfractionated heparin in a venous thrombosis model. The approximately 5-kDa fragment is an antithrombotic with several advantages: i) It is as active as unfractionated heparin in venous thrombosis, but it has little activity in arterial thrombosis; ii) It inhibits venous thrombosis with very little anticoagulant effect; iii) It does not cause bleeding; and iv) It is not obtained from mammals.

摘要

来自红藻西方软骨藻的硫酸化半乳聚糖具有强大的抗凝血活性,这归因于其能够增强抗凝血酶和/或肝素辅因子II对凝血酶和Xa因子的抑制作用。在动脉血栓形成中,它的活性低于未分级肝素,但在静脉血栓形成中呈现出双重作用,低剂量时抑制血栓形成,高剂量时则不然。这种对静脉血栓形成的双重作用是两种作用的结果,一种作用是抑制凝血酶和Xa因子,另一种作用是诱导XII因子激活。为了分离这些作用,我们制备了低分子量的硫酸化半乳聚糖衍生物。获得了两个大小与未分级肝素和低分子量肝素相似的级分。随着分子量降低,在抗凝血酶和肝素辅因子II存在下激活XII因子以及促进凝血蛋白酶抑制的能力减弱。在大约5 kDa时,硫酸化半乳聚糖片段对XII因子激活没有影响,并且在静脉血栓形成模型中显示出与未分级肝素相同的作用。大约5 kDa的片段是一种具有多种优势的抗血栓药物:i)在静脉血栓形成中它与未分级肝素活性相当,但在动脉血栓形成中活性很小;ii)它以非常小的抗凝血作用抑制静脉血栓形成;iii)它不会导致出血;iv)它不是从哺乳动物中获得的。

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