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Lonomia obliqua venom action on fibrinolytic system.

机译:茶树斜纹毒液对纤溶系统的作用。

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摘要

Accidental skin contact with the Lonomia caterpillar bristles causes a severe hemorrhagic syndrome. While fibrinolytic activation is considered to be the main cause of hemorrhage in Lonomia achelous envenomation, a consumptive coagulopathy was found to be a major component involved in the bleeding complications observed in patients envenomed by contact with Lonomia obliqua. Although we have previously observed that in L. obliqua envenomations, fibrinolysis activation appeared to be secondary to coagulation system activation, there are no reports regarding the ability of L. obliqua venom to activate directly fibrinolytic pathways. We examined the action of L. obliqua crude bristles extract (LOCBE) on several fibrinolytic system components. We demonstrated that LOCBE degraded the A-alpha fibrinogen chain only at high concentrations and after long incubation times. Under these conditions, LOCBE also induced prolongation of the fibrinogen clotting time, but no clot lysis was observed before 24 h. LOCBE didnot contain t-PA- or u-PA-like activities. Gel filtration and SDS-PAGE showed that LOCBE did not induce FXIII digestion. In addition, no FXIII activity inhibition was detected by dansylcadaverin method. FXIII levels remained unchanged when FXIII was measured in fibrinogen-depleted LOCBE-treated rat plasma, suggesting that the observed 50% FXIII reduction in rats was related to consumption. In conclusion, our results clearly demonstrated that LOCBE did not display either FXIII inhibition or degradation nor fibrinolytic activity. Furthermore, although proteolytic activity on Aalpha fibrinogen chain was observed, cross-linked fibrin was not affected by LOCBE.
机译:意外的皮肤接触Lonomia毛毛虫毛导致严重的出血综合征。尽管纤维蛋白溶解激活被认为是Lonomia恶性白癜风中出血的主要原因,但发现消耗性凝血病是与Lonomia obliqua接触的患者中观察到的出血并发症的主要成分。尽管我们以前已经观察到在L. obliqua毒液中,纤维蛋白溶解激活似乎是继凝血系统激活之后,但尚无关于L. obliqua毒液直接激活纤维蛋白溶解途径的能力的报道。我们检查了L. obliqua粗毛刷毛提取物(LOCBE)对几种纤溶系统组分的作用。我们证明LOCBE仅在高浓度下和长时间孵育后才降解A-α纤维蛋白原链。在这些条件下,LOCBE还可延长纤维蛋白原的凝结时间,但在24 h之前未观察到凝块溶解。 LOCBE不包含类似t-PA或u-PA的活动。凝胶过滤和SDS-PAGE表明LOCBE不诱导FXIII消化。另外,通过丹磺酰尸胺法未检测到FXIII活性抑制。当在纤维蛋白原耗尽的LOCBE处理的大鼠血浆中测量FXIII时,FXIII水平保持不变,这表明在大鼠中观察到的FXIII降低50%与消耗有关。总之,我们的结果清楚地表明,LOCBE既不显示FXIII抑制或降解,也不显示纤维蛋白溶解活性。此外,尽管观察到了对Aalpha纤维蛋白原链的蛋白水解活性,但交联的纤维蛋白不受LOCBE影响。

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