Apel C, Rícný J, Wagner G, Wessler I
Department of Pharmacology, University of Mainz, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 1995 Dec;352(6):646-52. doi: 10.1007/BF00171324.
Endplate preparations of the rat left hemidiaphragm were incubated with [3H]choline to label neuronal transmitter stores. Nerve evoked release of newly-synthesized [3H]acetylcholine was measured in the absence of cholinesterase inhibitors to investigate whether snake venom neurotoxins by blocking presynaptic nicotinic autoreceptors affect evoked transmitter release. Contractions of the indirectly stimulated hemidiaphragm were recorded to characterize the blocking effect of alpha-neurotoxins at the post-synaptic nicotinic receptors. Neither the long chain neurotoxins alpha-cobratoxin (1 microgram ml-1) and alpha-bungarotoxin (5 microgram ml-1) nor the short chain neurotoxin erabutoxin-b (0.1, 1 and 10 micrograms ml-1) affected the nerve-evoked release of [3H]acetylcholine. kappa-Bungarotoxin (1 and 5 micrograms ml-1), a toxin preferentially blocking neuronal nicotinic receptors, did also not affect evoked [3H]acetylcholine release, whereas (+)-tubocurarine (1 microM) under identical conditions reduced the release by about 50%. alpha-Bungarotoxin, alpha-cobratoxin and erabutoxin-b concentration-dependently (0.01-0.6 micrograms ml-1) inhibited nerve-evoked contractions of the hemidiaphragm. All neurotoxins except erabutoxin-b enhanced the basal tritium efflux immediately when applied to the endplate preparation or to a non-innervated muscle strip labelled with [3H]choline. This effect was attributed to an enhanced efflux of [3H]phosphorylcholine, whereas the efflux of [3H]choline and [3H]acetylcholine was not affected. It is concluded that the alpha-neurotoxins and kappa-bungarotoxin do not block presynaptic nicotinic receptors of motor nerves. These nicotinic autoreceptors differ from nicotinic receptors localized at the muscle membrane and at autonomic ganglia.
将大鼠左半膈肌的终板制剂与[3H]胆碱一起孵育,以标记神经元递质储存。在不存在胆碱酯酶抑制剂的情况下,测量神经诱发的新合成[3H]乙酰胆碱的释放,以研究蛇毒神经毒素通过阻断突触前烟碱型自身受体是否影响诱发的递质释放。记录间接刺激的半膈肌的收缩情况,以表征α-神经毒素对突触后烟碱型受体的阻断作用。长链神经毒素α-眼镜蛇毒素(1微克/毫升)和α-银环蛇毒素(5微克/毫升)以及短链神经毒素 erabutoxin-b(0.1、1和10微克/毫升)均未影响神经诱发的[3H]乙酰胆碱释放。κ-银环蛇毒素(1和5微克/毫升)是一种优先阻断神经元烟碱型受体的毒素,也未影响诱发的[3H]乙酰胆碱释放,而在相同条件下,(+)-筒箭毒碱(1微摩尔)使释放减少了约50%。α-银环蛇毒素、α-眼镜蛇毒素和 erabutoxin-b 浓度依赖性地(0.01-0.6微克/毫升)抑制半膈肌的神经诱发收缩。除 erabutoxin-b 外,所有神经毒素在应用于终板制剂或用[3H]胆碱标记的无神经支配肌肉条时,立即增强了基础氚外流。这种效应归因于[3H]磷酰胆碱外流的增强,而[3H]胆碱和[3H]乙酰胆碱的外流未受影响。结论是,α-神经毒素和κ-银环蛇毒素不阻断运动神经的突触前烟碱型受体。这些烟碱型自身受体不同于位于肌膜和自主神经节的烟碱型受体。