首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Biochemical characterization of the venom of the coral snake Micrurus tener and comparative biological activities in the mouse and a reptile model
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Biochemical characterization of the venom of the coral snake Micrurus tener and comparative biological activities in the mouse and a reptile model

机译:珊瑚蛇Micrurus tener毒液的生化特征以及在小鼠和爬行动物模型中的比较生物活性

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The objective of this study was to identify the venom components that could play a relevant role during envenomation caused by the coral snake Micrurus tener, through its biochemical characterization as well as the analysis of its effects on a murine model. Furthermore, it aimed to evaluate crude venom, in addition to its components, for possible specificity of action on a natural prey model (Conopsis lineata). The toxicity of the crude venom (delivered subcutaneously) showed a significant difference between the Median Lethal Dose (LD50) in mice (4.4 mu g/g) and in Conopsis lineata (12.1 mu g/g) that was not observed when comparing the Median Paralyzing Dose (PD50) values (mice = 4.7 mu g/g; snakes = 4.1 mu g/g). These results are evidence that the choice of study model strongly influences the apparent effects of crude venom. Moreover, based on the observed physical signs in the animal models, it was concluded that the most important physical effect caused by the venom is flaccid paralysis, which facilitates capture and subduing of prey regardless of whether it is alive; death is a logical consequence of the lack of oxygenation. Venom fractionation using a C-18 reverse phase column yielded 35 fractions from which 16.6% caused paralysis and/or death to both animal models, 21.9% caused paralysis and/or death only to C lineata and 1.6% were murine specific. Surprisingly, the diversity of snake-specific fractions did not reflect a difference between the PD(50)s of the crude venom in mice and snakes, making it impossible to assume some type of specificity for either of the study models. Finally, the great diversity and abundance of fractions with no observable effect in snakes or mice (42.7%) suggested that the observed lethal fractions are not the only relevant toxic fractions within the venom and emphasized the possible relevance of interaction between components to generate the syndrome caused by the venom as a whole. (C) 2013 Elsevier Ltd. All rights reserved.
机译:这项研究的目的是通过对其生化特性及其对鼠模型的影响进行分析,以确定在蛇毒snake虫的caused毒过程中可能起相关作用的毒液成分。此外,其目的在于评估粗毒液及其成分,以评估其对天然猎物模型(Conopsis lineata)的作用。粗毒(皮下递送)的毒性显示小鼠(4.4μg / g)和Conopsis lineata(12.1μg / g)中的致死剂量(LD50)之间存在显着差异,比较中位数时未观察到瘫痪剂量(PD50)值(小鼠= 4.7μg / g;蛇= 4.1μg / g)。这些结果证明,研究模型的选择强烈影响粗毒液的表观效果。此外,根据在动物模型中观察到的身体症状,可以得出结论,由毒液引起的最重要的物理作用是松弛性麻痹,无论其是否活着,它都有助于捕获和制服猎物。死亡是缺乏氧气的合理结果。使用C-18反相柱进行毒液分馏可得到35个馏分,其中16.6%导致两种动物模型瘫痪和/或死亡,21.9%仅导致C谱系麻痹和/或死亡,而1.6%具有鼠特异性。出人意料的是,蛇特异性组分的多样性并未反映出小鼠和蛇中粗毒的PD(50)之间的差异,因此无法对两种研究模型都假设某种类型的特异性。最后,在蛇或小鼠中没有可观察到的效应的组分的多样性和丰富性(42.7%)表明观察到的致死组分不是毒液中唯一相关的毒性组分,并强调了组分之间相互作用以产生综合征的可能相关性由毒液整体引起。 (C)2013 Elsevier Ltd.保留所有权利。

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