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硫酸皮肤素和对人血浆中抗凝血酶III具有高亲和力的五糖对因子X和因子V激活的抑制作用。

Inhibition of factor X and factor V activation by dermatan sulfate and a pentasaccharide with high affinity for antithrombin III in human plasma.

作者信息

Ofosu F A, Choay J, Anvari N, Smith L M, Blajchman M A

机构信息

Canadian Red Cross Society, Blood Transfusion Service, Hamilton.

出版信息

Eur J Biochem. 1990 Oct 24;193(2):485-93. doi: 10.1111/j.1432-1033.1990.tb19363.x.

Abstract

There is evidence that by catalyzing thrombin inhibition, several glycosaminoglycans can inhibit the thrombin-mediated amplification reactions of coagulation and thereby delay prothrombin activation. The two amplification reactions can apparently be catalysed by endogenously generated factor Xa and thrombin. This study provides evidence which suggests that on a molar basis, an agent which can only catalyse thrombin inhibition is approximately 10 times more effective than an agent which can only catalyse factor Xa inhibition in their ability to inhibit intrinsic prothrombin activation. We determined the concentrations of each of heparin, dermatan sulfate and a pentasaccharide with high affinity for antithrombin III, to delay intrinsic prothrombin activation for at least 15s. Heparin catalyses both thrombin and factor Xa inhibition; dermatan sulfate catalyses only thrombin inhibition, while the pentasaccharide only catalyses factor Xa inhibition. Efficient prothrombin activation, which coincided with both factor X activation and factor V proteolysis, was first observed 45s after CaC12 was added to contact-activated plasma. Heparin (approximately 0.1 microM) prolonged by at least 30 s the time required for the activation of the three clotting factors to begin. The minimum concentrations of the pentasaccharide and dermatan sulfate to delay the activation of prothrombin, factors X and V were approximately 50 microM and approximately 5 microM, respectively. Thus, each anticoagulant could inhibit intrinsic prothrombin activation only when it inhibited activation of both factors X and V. A combination of approximately 5 microM pentasaccharide and approximately 0.05 microM dermatan sulfate similarly delayed the activation of all three clotting factors. Thus, while catalysis of thrombin inhibition is a more effective pathway than catalysis of factor Xa inhibition for delaying prothrombin activation, the simultaneous catalysis of thrombin and factor Xa inhibition can synergistically improve the ability of a sulfated polysaccharide to delay prothrombin activation.

摘要

有证据表明,几种糖胺聚糖通过催化凝血酶抑制作用,可抑制凝血酶介导的凝血放大反应,从而延迟凝血酶原激活。这两种放大反应显然可由内源性生成的因子Xa和凝血酶催化。本研究提供的证据表明,以摩尔计,一种只能催化凝血酶抑制的试剂在抑制内源性凝血酶原激活的能力方面,比一种只能催化因子Xa抑制的试剂约有效10倍。我们测定了肝素、硫酸皮肤素和对抗凝血酶III具有高亲和力的五糖各自的浓度,以延迟内源性凝血酶原激活至少15秒。肝素催化凝血酶和因子Xa抑制;硫酸皮肤素仅催化凝血酶抑制,而五糖仅催化因子Xa抑制。在向接触激活的血浆中加入CaC12后45秒首次观察到与因子X激活和因子V蛋白水解同时发生的高效凝血酶原激活。肝素(约0.1 microM)将三种凝血因子开始激活所需的时间延长了至少30秒。延迟凝血酶原、因子X和因子V激活的五糖和硫酸皮肤素的最低浓度分别约为50 microM和约5 microM。因此,每种抗凝剂只有在抑制因子X和因子V的激活时才能抑制内源性凝血酶原激活。约5 microM五糖和约0.05 microM硫酸皮肤素的组合同样延迟了所有三种凝血因子的激活。因此,虽然催化凝血酶抑制是比催化因子Xa抑制更有效的延迟凝血酶原激活的途径,但同时催化凝血酶和因子Xa抑制可协同提高硫酸化多糖延迟凝血酶原激活的能力。

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