蛇毒诱发独特肺血栓形成效应的小鼠实验模型

Alexandra Rucavado, Erika Camacho, Teresa Escalante, Bruno Lomonte, Julian Fernandez, Daniela Solano, Isabel Quiros-Gutierrez, Gabriel Ramirez-Vargas, Karol Vargas, Ivette Arguello, Alejandro Navarro, Carlos Abarca, Alvaro Segura, Jonathan Florentin, Hatem Kallel, Dabor Resiere, Remi Neviere, Jose Maria Gutierrez
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引用次数: 0

摘要

背景小安的列斯群岛马提尼克岛特有的一种蝰蛇--Bothrops lanceolatus的毒液可诱发一种独特的临床表现,即血栓形成。以往的临床观察表明,血栓形成在被幼蛇咬伤的患者中更为常见。方法/主要研究结果通过(a)描述其蛋白质组,(b)评估其在小鼠模型中诱导血栓形成的能力,以及(c)评估其体外促凝血活性和体内止血变化,对幼年和成年长尾蝰标本的毒液进行了比较。幼体和成体标本的毒液蛋白质组非常相似。通过腹腔注射途径,幼体标本的毒液会在肺血管中形成大量血栓,而成体标本的毒液则很少出现这种情况。金属蛋白酶抑制剂 Batimastat 不能抑制血栓形成。两种毒液对柠檬酸化小鼠血浆和牛纤维蛋白原都有微弱的体外促凝作用。静脉注射毒液不会影响传统的凝血测试(凝血酶原时间和活化部分凝血活酶时间),但会导致部分纤维蛋白原浓度下降。幼体标本的毒液在静脉注射后会引起一些旋转血栓弹性测定参数的部分改变。在静脉注射毒液时未观察到凝血试验的改变,但幼体和成体毒液会引起明显的血小板减少。尽管观察到幼体和成体毒液蛋白质组相似,但幼体标本毒液的这种效应更为明显。成体和幼体毒液不会诱发其他两栖类毒液特有的消耗性凝血病。两种毒液都会诱发明显的血小板减少症。该实验模型再现了这些毒液中毒的主要临床表现,有助于了解这种血栓作用的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A murine experimental model of the unique pulmonary thrombotic effect induced by the venom of the snake Bothrops lanceolatus
Background The venom of Bothrops lanceolatus, a viperid species endemic to the Lesser Antillean Island of Martinique, induces a unique clinical manifestation, i.e., thrombosis. Previous clinical observations indicate that thromboses are more common in patients bitten by juvenile specimens. There is a need to develop an experimental model of this effect in order to study the mechanisms involved. Methodology/principal findings The venoms of juvenile and adult specimens of B. lanceolatus were compared by (a) describing their proteome, (b) assessing their ability to induced thrombosis in a mouse model, and (c) evaluating their in vitro procoagulant activity and in vivo hemostasis alterations. Venom proteomes of juvenile and adult specimens were highly similar. When injected by the intraperitoneal (i.p.) route, the venom of juvenile specimens induced the formation of abundant thrombi in the pulmonary vasculature, whereas this effect was less frequent in the case of adult venom. Thrombosis was not abrogated by the metalloproteinase inhibitor Batimastat. Both venoms showed a weak in vitro procoagulant effect on citrated mouse plasma and bovine fibrinogen. When administered intravenously (i.v.) venoms did not affect classical clotting tests (prothrombin time and activated partial thromboplastin time) but caused a partial drop in fibrinogen concentration. The venom of juvenile specimens induced partial alterations in some rotational thromboelastometry parameters after i.v. injection. No alterations in coagulation tests were observed when venoms were administered i.p., but juvenile and adult venoms induced a marked thrombocytopenia. Conclusions/significance An experimental model of the thrombotic effect induced by B. lanceolatus venom was developed. This effect is more pronounced in the case of venom of juvenile specimens, despite the observation that juvenile and adult venom proteomes are similar. Adult and juvenile venoms do not induce a consumption coagulopathy characteristic of other Bothrops sp venoms. Both venoms induce a conspicuous thrombocytopenia. This experimental model reproduces the main clinical findings described in these envenomings and should be useful to understand the mechanisms of this thrombotic effect.
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