Morphological abnormalities in myelinated nerve fibres caused by Leiurus, Centruroides and Phoneutria venoms and their prevention by tetrodotoxin.

S Love, M A Cruz-Höfling, L W Duchen
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引用次数: 23

Abstract

Morphological changes in peripheral nerve caused by the venoms of the scorpions Leiurus quinquestriatus and Centruroides sculpturatus were compared with those caused by Phoneutria nigriventer spider venom. Both scorpion venoms are known to delay the inactivation of sodium currents, Centruroides venom also altering the voltage dependence of sodium gating. Venom was injected by means of a glass micropipette into the sciatic nerves of anaesthetized mice. After survival times ranging from 15 min to 24 h the nerves were examined by light and electron microscopy. The two scorpion venoms caused alterations virtually identical to those produced by Phoneutria venom, which included swelling of the nodal axoplasm and accumulation of fluid in the periaxonal space of myelinated fibres. These alterations were most marked after 1 to 2 h and had largely disappeared by 24 h. Pre-treatment of the nerves with tetrodotoxin, which specifically blocks sodium channels, completely prevented both the nodal axoplasmic swelling and the periaxonal oedema. It seems likely that these effects result from an action common to the three venoms and that this is probably a delay in the inactivation of sodium current at the node of Ranvier.

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河豚毒素引起的有髓神经纤维形态异常及河豚毒素的预防。
本文比较了五角蝎(Leiurus quinquestriatus)和石纹蝎(Centruroides sculpturatus)与黑音蛛(Phoneutria nigriventer)蜘蛛毒液引起的周围神经形态学变化。已知这两种蝎子的毒液都能延缓钠电流的失活,森特罗氏毒液还能改变钠门控的电压依赖性。用玻璃微管将毒液注入麻醉小鼠坐骨神经。存活15分钟至24小时后,用光镜和电镜检查神经。这两种蝎子毒液引起的变化与声母蛇毒几乎相同,包括结节轴质肿胀和髓鞘纤维轴周间隙液体积聚。这些变化在1 - 2小时后最为明显,24小时后基本消失。用河豚毒素预处理神经,其特异性阻断钠通道,完全阻止了淋巴结轴浆肿胀和轴周水肿。这些影响似乎可能是由三种毒液共同的作用引起的,这可能是兰维耶结钠电流失活的延迟。
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The school of Bernard Katz. London, 5 April 1989. Proceedings. Extracellular magnesium regulates acetylcholine-evoked amylase secretion and calcium mobilization in rat pancreatic acinar cells. Structure and function of the carotid body in New Zealand genetically hypertensive rats. Intracellular signalling and regulation of gastric acid secretion. Metabolism and inactivation of gastrin releasing peptide by endopeptidase-24.11 in the dog.
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