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通过FDP片段分析鉴别纤维蛋白溶解和纤维蛋白原溶解

[Differentiation of fibrinolysis and fibrinogenolysis by analysis of FDP fragments].

作者信息

Okumura N, Furuwatari C, Ishikawa S, Furihata K, Katsuyama T, Kanai M, Nakahata T, Saitoh H

机构信息

Central Clinical Laboratories, Shinshu University Hospital, Matsumoto.

出版信息

Rinsho Byori. 1992 Jul;40(7):789-94.

PMID:1507499
Abstract

We previously analysed the fragments of fibrin/fibrinogen degradation products (FDP) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) combined with immunoblotting. In this report, we studied the semi-quantitative analysis of fibrinolysis (degradation of cross-linked fibrin) and fibrinogenolysis (degradation of fibrinogen and/or unstable fibrin) of patients' samples by our method. In vitro study of FDP made it clear that an appearance of D fragment confirmed fibrinogenolysis and an appearance of DD fragment and/or high molecular weight fragments which have higher molecular weight than DY or X fragment confirmed fibrinolysis. In addition, a study with mixtures of various concentrations of fibrin degradation products (FbDP) and fibrinogen degradation products (FgDP) demonstrated a dose dependent intensity of band by immunoblot method. These results show that our method is favorable for the semi-quantitative analysis of fibrinolysis and fibrinogenolysis. We applied the method to 6 samples from patients with disseminated intravascular coagulation (DIC). Consequently, fibrinogenolysis was observed in all of 6 samples, in which fibrinogenolysis was more enhanced than fibrinolysis in one sample, and an equivalent degree of fibrinolysis and fibrinogenolysis were observed in 3 of 6 samples. Although our method was probably devoid of the ability to distinguish FgDP from degradation products of unstable fibrin, these findings indicate that fibrinogenolysis is, at any rate, enhanced in the majority of patients with DIC, besides fibrinolysis.

摘要

我们之前通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)结合免疫印迹法分析了纤维蛋白/纤维蛋白原降解产物(FDP)的片段。在本报告中,我们用我们的方法研究了患者样本中纤维蛋白溶解(交联纤维蛋白的降解)和纤维蛋白原溶解(纤维蛋白原和/或不稳定纤维蛋白的降解)的半定量分析。对FDP的体外研究表明,D片段的出现证实了纤维蛋白原溶解,而DD片段和/或分子量高于DY或X片段的高分子量片段的出现证实了纤维蛋白溶解。此外,对不同浓度的纤维蛋白降解产物(FbDP)和纤维蛋白原降解产物(FgDP)混合物的研究通过免疫印迹法显示了条带强度的剂量依赖性。这些结果表明,我们的方法有利于纤维蛋白溶解和纤维蛋白原溶解的半定量分析。我们将该方法应用于6例弥散性血管内凝血(DIC)患者的样本。结果,在所有6个样本中均观察到纤维蛋白原溶解,其中1个样本中纤维蛋白原溶解比纤维蛋白溶解更增强,在6个样本中的3个样本中观察到纤维蛋白溶解和纤维蛋白原溶解程度相当。尽管我们的方法可能缺乏区分FgDP与不稳定纤维蛋白降解产物的能力,但这些发现表明,除纤维蛋白溶解外,大多数DIC患者的纤维蛋白原溶解无论如何都会增强。

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