Gorio A, Rubin L L, Mauro A
J Neurocytol. 1978 Apr;7(2):193-202. doi: 10.1007/BF01217918.
Black widow spider venom (BWSV) contains a toxin, alpha-latrotoxin, which is capable of stimulating vesicle release, resulting eventually in depletion of vesicles and block of neuromuscular transmission at the frog neuromuscular junction. Since it has been shown that alpha-latrotoxin very markedly increases the cation conductance of artificial lipid bilayers, it was postulated that BWSV stimulates release by opening channels permeable to Ca2+ and, in the case of Ca2+-free Ringer's, to Na+ which would release Ca2+ from intracellular stores. To test this hypothesis we chose as a sodium substitute, glucosamine, which is impermeable to the venom-induced channels in the lipid bilayers and to the postsynaptic membrane of the frog neuromuscular junction. Electron microscopical analysis showed that up to 75 min perfusion in Na+ and Ca2+-free medium did not alter the ultrastructure of the nerve terminals. However when BWSV was applied in this medium a significant depletion was noticeable within 15 min and after 60 min the terminals were depleted of vesicles whereas the mitochondria were unchanged in number and structure. If BWSV is applied for 60 min in glucosamine Ringer's containing 1.8 mM Ca2+, most of the nerve terminals still have synaptic vesicles scattered in the cytoplasm or clustered around amorphous structures and the mitochondria are swollen. Application of large doses of BWSV in low Ca2+ Ringer's leads to damage of the mitochondria and to very pronounced swelling of the nerve endings, whereas this is not observed if the dose of venom is applied in Na+-free and Ca2+-free Ringer's. Electrophysiological recording showed that neuromuscular transmission is already blocked after 15 min treatment with BWSV in glucosamine-Ringer's. From these results we conclude that BWSV increases the conductance of the nerve terminal membrane to cations such as Na+ and Ca2+ and stimulates release by a mechanism which may not involve its ionophore property.
黑寡妇蜘蛛毒液(BWSV)含有一种毒素,α- latrotoxin,它能够刺激囊泡释放,最终导致囊泡耗尽并阻断青蛙神经肌肉接头处的神经肌肉传递。由于已经表明α- latrotoxin非常显著地增加了人工脂质双层的阳离子电导,因此推测BWSV通过打开对Ca2+ 通透的通道来刺激释放,并且在无Ca2+ 的林格氏液中,对Na+ 通透,而Na+ 会从细胞内储存中释放Ca2+ 。为了验证这一假设,我们选择了葡糖胺作为钠替代物,它对脂质双层中由毒液诱导的通道以及青蛙神经肌肉接头的突触后膜是不通透的。电子显微镜分析表明,在无Na+ 和Ca2+ 的培养基中灌注长达75分钟并没有改变神经末梢的超微结构。然而,当在这种培养基中应用BWSV时,在15分钟内就明显观察到显著的耗尽,60分钟后末梢的囊泡耗尽,而线粒体的数量和结构没有变化。如果在含有1.8 mM Ca2+ 的葡糖胺林格氏液中应用BWSV 60分钟,大多数神经末梢仍然有突触囊泡分散在细胞质中或聚集在无定形结构周围,并且线粒体肿胀。在低Ca2+ 的林格氏液中应用大剂量的BWSV会导致线粒体损伤和神经末梢非常明显的肿胀,而如果在无Na+ 和无Ca2+ 的林格氏液中应用毒液剂量则不会观察到这种情况。电生理记录表明,在用葡糖胺 - 林格氏液中的BWSV处理15分钟后神经肌肉传递就已经被阻断。从这些结果我们得出结论,BWSV增加了神经末梢膜对Na+ 和Ca2+ 等阳离子的电导,并通过一种可能不涉及其离子载体特性的机制刺激释放。