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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Inhibition of the generation of thrombin and factor Xa by a fucoidan from the brown seaweed Ecklonia kurome.
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Inhibition of the generation of thrombin and factor Xa by a fucoidan from the brown seaweed Ecklonia kurome.

机译:褐藻海藻Ecklonia kurome中的岩藻依聚糖对凝血酶和Xa因子的抑制作用。

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摘要

The effects of a fucoidan (C-II), which was purified from the brown seaweed Ecklonia kurome, on the generation of thrombin and factor Xa have been investigated by measuring the amidolytic activities by using the respective specific chromogenic substrates in both plasma and purified systems. C-II inhibited significantly the generation of thrombin in both the intrinsic and the extrinsic pathways, although the intrinsic inhibitory effect by C-II was more remarkable than the extrinsic one. On the other hand, C-II was a good inhibitor of the factor Xa generation in the intrinsic pathway, while it was a poor one in the extrinsic pathway. In the purified systems C-II also inhibited the formation of prothrombin-activating complex (i.e., prothrombinase), but not its activity. The concentration of C-II required for 50% inhibition of thrombin generation was about one-tenth to one-seventh of that of the activity of the generated thrombin in plasma. These results indicate that C-II has an inhibitory effect on the generation of thrombin by blocking the formation of prothrombinase and by preventing the generation of intrinsic factor Xa in addition to its antithrombin activity, and also that the generation-inhibitory effect is more remarkable than C-II's enhancement effect on the antithrombin activity by heparin cofactor II in plasma.
机译:通过在血浆和纯化系统中使用各自的特定生色底物测量酰胺分解活性,研究了从褐藻海藻Ecklonia kurome纯化的岩藻依聚糖(C-II)对凝血酶和Xa因子产生的影响。 。尽管C-II的内在抑制作用比外源性途径更显着,但C-II在内在和外在途径中均显着抑制了凝血酶的产生。另一方面,C-II是内源途径中Xa因子生成的良好抑制剂,而在外源途径中则较弱。在纯化的系统中,C-Ⅱ也抑制凝血酶原活化复合物(即凝血酶原酶)的形成,但不抑制其活性。抑制凝血酶产生所需的C-II浓度约为血浆中所产生凝血酶活性的十分之一至七分之一。这些结果表明,C-II除了具有抗凝血酶活性外,还可以通过阻止凝血酶原酶的形成和阻止内在因子Xa的产生来抑制凝血酶的产生,并且其抑制作用比C-II对血浆中肝素辅因子II抗凝血酶活性的增强作用。

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