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促凝血活性磷脂含量是兔体内凝血酶原复合物(因子IX)浓缩物体内血栓形成性的主要决定因素。

The coagulant-active phospholipid content is a major determinant of in vivo thrombogenicity of prothrombin complex (Factor IX) concentrates in rabbits.

作者信息

Giles A R, Nesheim M E, Hoogendoorn H, Tracy P B, Mann K G

出版信息

Blood. 1982 Feb;59(2):401-7.

PMID:7034817
Abstract

In vitro evaluation of prothrombin complex concentrates in a thrombin generation assay, using DAPA and purified components of the prothrombinase complex, demonstrated significant levels of coagulant-active "phospholipid replacing" activity. Quantification of this activity showed a significant correlation (r = 0.8747, p less than 0.01) with thrombogenicity measured in vivo in a stasis model in rabbits. Extracted lipid material retained full phospholipid replacing activity in the vitro assay. Thin-layer chromatographic characterization confirmed the presence of phospholipids with known coagulant activity in vitro. In vivo, the extracted material was nonthrombogenic but augmented the thrombogenicity of purified factor Xa. Substitution of a synthetic coagulant-active phospholipid (phosphatidylcholine-phosphatidylserine lipid vesicles) for the extracted phospholipid produced a similar augmentation of a factor-Xa-induced thrombogenicity in vivo. It is concluded that the coagulant-active phospholipid content of prothrombin complex concentrates is a major determinant of thrombogenicity but requires the presence of activated clotting factors for its expression in vivo.

摘要

在凝血酶生成试验中,使用达比加群酯(DAPA)和凝血酶原酶复合物的纯化成分对凝血酶原复合物浓缩物进行体外评估,结果显示出显著水平的具有凝血活性的“磷脂替代”活性。对该活性的定量分析表明,其与在兔淤滞模型中体内测量的血栓形成性具有显著相关性(r = 0.8747,p < 0.01)。提取的脂质材料在体外试验中保留了完全的磷脂替代活性。薄层色谱表征证实了体外存在具有已知凝血活性的磷脂。在体内,提取的材料不具有血栓形成性,但增强了纯化的因子Xa的血栓形成性。用合成的具有凝血活性的磷脂(磷脂酰胆碱 - 磷脂酰丝氨酸脂质体)替代提取的磷脂,在体内产生了类似的因子Xa诱导的血栓形成性增强。得出的结论是,凝血酶原复合物浓缩物中具有凝血活性的磷脂含量是血栓形成性的主要决定因素,但在体内表达时需要有活化的凝血因子存在。

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