Goularte F C, da Cruz-Höfling M A, Corrado A P, Rodrigues-Simioni L
Department of Pharmacology, Faculty of Medical Sciences, State University of Campinas (UNICAMP), Brazil.
Acta Physiol Pharmacol Ther Latinoam. 1999;49(4):290-6.
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.
黑带珊瑚蛇是中美洲数量最多的珊瑚蛇。这种蛇的毒液在37摄氏度孵育的离体小鼠膈神经-膈肌标本中可引起浓度依赖性(10 - 20微克/毫升)的去极化。筒箭毒碱(10微克/毫升)和αβ银环蛇毒素(3 - 5微克/毫升)能够部分保护标本免受毒液(10微克/毫升)诱导的去极化,提示突触后胆碱能受体参与其中。这种毒液(10微克/毫升)在孵育的最初10 - 20分钟内还增加了微小终板电位(mepps)的频率和幅度。随后,微小终板电位逐渐降低并在60分钟后消失。这些反应伴随着涉及神经末梢、突触后连接褶和肌肉线粒体的超微结构变化。突触沟变浅,并且经常出现带有ω形轴膜凹陷的“收缩”末梢以及突触小泡数量减少。一个常见的发现是在末梢与施万细胞或突触后肌膜之间存在许多指状、膜包绕的小体。毒液与特异性抗蛇毒血清预孵育或标本在室温(24 - 26摄氏度)孵育可减少超微结构改变的数量和强度。最后这一发现提示毒液中存在的一种酶促过程,可能是磷脂酶A2参与其中。毒液诱导的电生理和超微结构效应之间存在良好的相关性,这使我们能够得出结论,黑带珊瑚蛇毒液在中毒初期具有突触前作用,随后出现突触下和突触后效应,最后一种效应是神经肌肉阻滞的最重要原因。毒液对肌肉纤维的直接作用也可能导致不可逆的阻滞。