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用血栓描记术测定的血浆中可逆转的凝血酶抑制剂对凝血酶生成的矛盾性刺激是由α-巨球蛋白-凝血酶引起的。

The paradoxical stimulation by a reversible thrombin inhibitor of thrombin generation in plasma measured with thrombinography is caused by alpha-macroglobulin-thrombin.

机构信息

Synapse BV, Cardiovascular Research Institute Maastricht, Oxfordlaan, Maastricht, the Netherlands.

出版信息

J Thromb Haemost. 2010 Jun;8(6):1281-9. doi: 10.1111/j.1538-7836.2010.03822.x. Epub 2010 Feb 24.

Abstract

BACKGROUND

Thrombin generation (TG) in plasma can be monitored continuously with a fluorogenic thrombin substrate using calibrated automated thrombinography (CAT). In the presence of low concentrations of a reversible direct thrombin inhibitor (DTI), CAT shows an unexpected effect: the endogenous thrombin potential (ETP) increases at low concentrations of the inhibitor to subsequently decrease concentration dependently at higher concentrations (> approximately 100 nm).

OBJECTIVES

To find an explanation for this phenomenon, we measured the concentrations of free thrombin and alpha(2)-macroglobulin-thrombin complex (alpha(2)MT) with a sub-sampling technique in the presence of AR-H067637, a selective DTI.

RESULTS

At all concentrations of the DTI there was a gradual dose-dependent decrease in the concentration of free, not-inhibited thrombin but a transient increase in free alpha(2)MT due to competition of thrombin and alpha(2)MT for the inhibitor. Because the CAT technique uses an algorithm to subtract alpha(2)MT activity from the total amidolytic activity, this transient increase in alpha(2)MT activity is not subtracted and erroneously attributed to thrombin itself.

CONCLUSIONS

This study explains the spurious increase in ETP observed at low DTI concentrations. The results obtained in plasma were corroborated by observations in a thrombin generating system reconstituted with purified factors. In practise, the effect of DTIs on TG can be reliably evaluated from the area under the curve till time-to-peak.

摘要

背景

使用荧光法凝血酶底物,通过校准自动凝血描记术(CAT)可以连续监测血浆中的凝血酶生成(TG)。在低浓度可逆直接凝血酶抑制剂(DTI)存在的情况下,CAT 显示出一种意想不到的效果:内源性凝血酶潜能(ETP)在低浓度抑制剂下增加,随后在较高浓度(>约 100nm)下浓度依赖性降低。

目的

为了解释这一现象,我们在存在选择性 DTI-AR-H067637 的情况下,使用亚采样技术测量了游离凝血酶和 α2-巨球蛋白-凝血酶复合物(α2MT)的浓度。

结果

在 DTI 的所有浓度下,未受抑制的游离凝血酶的浓度逐渐呈剂量依赖性下降,但由于凝血酶和 α2MT 与抑制剂竞争,游离 α2MT 短暂增加。由于 CAT 技术使用算法从总酰胺酶活性中减去 α2MT 活性,因此这种 α2MT 活性的短暂增加不会被减去,并错误地归因于凝血酶本身。

结论

本研究解释了在低 DTI 浓度下观察到的 ETP 假性增加。在与纯化因子重建的凝血酶生成系统中获得的结果得到了血浆中观察结果的证实。在实践中,可以从曲线下面积到达峰时间可靠地评估 DTI 对 TG 的影响。

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