黑微蛇蛇毒致神经肌肉阻滞及微毒性的电生理及超微结构分析。

F C Goularte, M A da Cruz-Höfling, A P Corrado, L Rodrigues-Simioni
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引用次数: 0

摘要

Micrurus nigrocinctus是中美洲数量最多的珊瑚蛇。在37℃下孵育的离体小鼠膈神经隔膜制剂中,该物种的毒液诱导了浓度依赖性(10-20微克/毫升)的去极化。d-Tubocurarine(10微克/毫升)和(α - β - ungarotoxin(3-5微克/毫升)能够部分抵抗该毒液(10微克/毫升)诱导的去极化,提示突触下胆碱能受体的参与。该毒液(10微克/毫升)也增加了微型终板电位(mepps)的频率和振幅在孵育的前10-20分钟。随后,mepps逐渐减少,并在60 min后消失。这些反应伴随着涉及神经末梢、突触下连接褶皱和肌肉线粒体的超微结构变化。突触沟很浅,经常出现“萎缩”的终末,有ω形的腋膜凹陷,突触囊泡数量减少。一个常见的发现是在终末和雪旺细胞或突触后肌膜之间存在大量的指状、膜包围的小体。与特异性抗蛇毒血清一起预孵育或在室温(24-26℃)下孵育,可减少超微结构改变的数量和强度。最后一项发现表明,毒液中存在一种酶促过程,可能是磷脂酶A2。有良好的相关性引起的电生理和超微结构的影响的毒液使我们得出这样的结论:m . nigrocinctus毒液有突触前动作中毒的初始阶段是由子任务和突触后的效果,最后被神经肌肉阻滞的最重要原因。毒液对肌纤维的直接作用也可能导致不可逆的阻滞。
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Electrophysiological and ultrastructural analysis of the neuromuscular blockade and miotoxicity induced by the Micrurus nigrocinctus snake venom.

Micrurus nigrocinctus is the most abundant coral snake in Central America. The venom of this specie induced a concentration-dependent (10-20 micrograms/ml) depolarization in the isolated mouse phrenic nerve-diaphragm preparations incubated at 37 degrees C. d-Tubocurarine (10 micrograms/ml) and (alpha beta ungarotoxin (3-5 micrograms/ml) were able to partially protect against the depolarization induced by the venom (10 micrograms/ml), suggesting the involvement of subsynaptic cholinergic receptors. This venom (10 micrograms/ml) also increased the frequency and amplitude of miniature end-plate potentials (mepps) during the first 10-20 min of incubation. Subsequently, the mepps progressively decreased and disappeared after 60 min. These responses were accompanied by ultrastructural changes involving the nerve terminals, the subsynaptic junctional folds and the muscle mitochondria. The synaptic gutter was shallow and, very often, "shrunken" terminals with omega-shaped axolemmal indentations and a decreased number of synaptic vesicles were present. A common finding was the presence of numerous finger-like, membrane-bounded bodies interposed between the terminal and the Schwann cells or postsynaptic sarcolemma. The preincubation of the venom with specific antivenom or the incubation of the preparations at room temperature (24-26 degrees C) reduced the number and intensity of the ultrastructural alterations. The last finding suggests the involvement of a enzymatic process, probably a phospholipase A2, present in the venom. There was a good correlation between the electrophysiological and ultrastructural effects induced by the venom which allow us to conclude that M. nigrocinctus venom has a presynaptic action in the initial stages of intoxication followed by sub- and postsynaptic effects, the last being the most important cause of neuromuscular blockade. A direct action of the venom on muscle fibers may also contributes to the irreversible blockade.

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