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巨蜥毒液通过破坏性切割破坏人纤维蛋白原的凝血能力。

Varanid Lizard Venoms Disrupt the Clotting Ability of Human Fibrinogen through Destructive Cleavage.

机构信息

Venom Evolution Lab, School of Biological Sciences, University of Queensland, St Lucia, QLD 4072, Australia.

Alphabiotoxine Laboratory sprl, Barberie 15, 7911 Montroeul-au-bois, Belgium.

出版信息

Toxins (Basel). 2019 May 7;11(5):255. doi: 10.3390/toxins11050255.

Abstract

The functional activities of Anguimorpha lizard venoms have received less attention compared to serpent lineages. Bite victims of varanid lizards often report persistent bleeding exceeding that expected for the mechanical damage of the bite. Research to date has identified the blockage of platelet aggregation as one bleeding-inducing activity, and destructive cleavage of fibrinogen as another. However, the ability of the venoms to prevent clot formation has not been directly investigated. Using a thromboelastograph (TEG5000), clot strength was measured after incubating human fibrinogen with and lizard venoms. Clot strengths were found to be highly variable, with the most potent effects produced by incubation with venoms from the and clades. The most fibrinogenolytically active venoms belonged to arboreal species and therefore prey escape potential is likely a strong evolutionary selection pressure. The results are also consistent with reports of profusive bleeding from bites from other notably fibrinogenolytic species, such as . Our results provide evidence in favour of the predatory role of venom in varanid lizards, thus shedding light on the evolution of venom in reptiles and revealing potential new sources of bioactive molecules useful as lead compounds in drug design and development.

摘要

与蛇类谱系相比,蚓蜥目蜥蜴毒液的功能活性受到的关注较少。巨蜥科蜥蜴的咬伤受害者经常报告持续出血,超过咬伤造成的机械损伤所预期的出血量。迄今为止的研究已经确定了血小板聚集的阻断是一种引起出血的活性,纤维蛋白原的破坏裂解是另一种。然而,毒液防止血栓形成的能力尚未被直接研究。使用血栓弹性图(TEG5000),在孵育人纤维蛋白原与 和 蜥蜴毒液后测量血凝块强度。发现血凝块强度高度可变,与来自 和 进化枝的 毒液孵育产生的最强效。最具纤维蛋白原裂解活性的毒液属于树栖物种,因此捕食逃避潜力可能是强烈的进化选择压力。这些结果也与来自其他明显纤维蛋白原裂解物种(如)咬伤导致大量出血的报告一致。我们的结果为毒液在巨蜥科蜥蜴中的捕食作用提供了证据,从而揭示了毒液在爬行动物中的进化,并揭示了作为药物设计和开发中先导化合物有用的潜在新生物活性分子来源。

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