Loring R H, Chiappinelli V A, Zigmond R E, Cohen J B
Neuroscience. 1984 Apr;11(4):989-99. doi: 10.1016/0306-4522(84)90209-4.
Bungarus multicinctus venom was fractionated by ion exchange chromatography and the various fractions were assayed for their ability to block synaptic transmission through the chick ciliary ganglion. alpha-Bungarotoxin purified from this venom failed to block transmission at 50 micrograms/ml. A second neurotoxin, which we designate Toxin F, blocked transmission at 1-3 micrograms/ml and also blocked ganglionic depolarizations induced by carbachol. Toxin F was clearly distinguishable from alpha-bungarotoxin on the basis of molecular weight (estimated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis) and isoelectric point. Binding assays revealed that 125I-labeled toxin F bound to two sites in the ciliary ganglion: one site that was shared by alpha-bungarotoxin and toxin F and another site that was recognized solely by toxin F. Carbachol and d-tubocurarine displaced only that [125I]toxin F bound to the shared site and had no effect on [125I]toxin F bound to the site recognized by toxin F alone. The results suggest that toxin F blocks synaptic transmission in the chick ciliary ganglion by a postsynaptic mechanism. Further study is required to determine whether this effect of toxin F is mediated through a direct interaction with ganglionic nicotinic receptors.
用离子交换色谱法分离银环蛇毒,并检测各组分阻断鸡睫状神经节突触传递的能力。从这种毒液中纯化得到的α-银环蛇毒素在50微克/毫升时未能阻断传递。另一种神经毒素,我们命名为毒素F,在1-3微克/毫升时可阻断传递,并且还能阻断卡巴胆碱诱导的神经节去极化。根据分子量(通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳估算)和等电点,毒素F与α-银环蛇毒素明显不同。结合试验表明,125I标记的毒素F与睫状神经节中的两个位点结合:一个位点是α-银环蛇毒素和毒素F共有的,另一个位点是毒素F单独识别的。卡巴胆碱和d-筒箭毒碱只能置换与共有位点结合的[125I]毒素F,而对与毒素F单独识别的位点结合的[125I]毒素F没有影响。结果表明,毒素F通过突触后机制阻断鸡睫状神经节的突触传递。需要进一步研究以确定毒素F的这种作用是否通过与神经节烟碱受体的直接相互作用介导。