Wilson H I, Nicholson G M, Tyler M I, Howden M E
Department of Health Sciences, University of Technology, Sydney, Broadway NSW, Australia.
Naunyn Schmiedebergs Arch Pharmacol. 1995 Jul;352(1):79-87. doi: 10.1007/BF00169193.
The present study investigated the action of textilotoxin, isolated from the venom of the Australian common brown snake Pseudonaja textilis, on neuromuscular transmission in isolated toad nerve-muscle preparations. Initial muscle twitch tension experiments revealed a triphasic pattern of changes in muscle tension and a irreversible binding action of textilotoxin (10 micrograms/ml) similar to other snake beta-neurotoxins. This was characterised by an initial depression of twitch tension, followed by a period of enhanced tension, eventually leading to a reduction in tension to complete neuromuscular blockade. These actions on muscle tension were investigated further by assessing the action of textilotoxin on end-plate potential amplitude (EPP). This revealed a similar triphasic alteration of the nerve-evoked release of acetylcholine from the motor nerve terminal. These actions on acetylcholine release were confirmed to be of a presynaptic origin since the modal amplitude of miniature end-plate potentials (MEPPs) was not reduced and in twitch tension experiments the muscle still contracted in response to direct muscle stimulation when nerve-evoked release was completely blocked. Interestingly dramatic effects were observed on the spontaneous release of acetylcholine, including an marked increase in MEPP frequency, a skewing of the MEPP amplitude frequency histogram to the right, and a resultant increase in the number of 'giant' MEPPs. These results indicate that textilotoxin causes a presynaptic blockade of neuromuscular transmission involving a disruption of the regulatory mechanism that controls acetylcholine release.
本研究调查了从澳大利亚普通棕蛇(细鳞太攀蛇)毒液中分离出的类凝血酶毒素对离体蟾蜍神经-肌肉标本神经肌肉传递的作用。最初的肌肉抽搐张力实验揭示了肌肉张力变化的三相模式,以及类凝血酶毒素(10微克/毫升)与其他蛇β-神经毒素相似的不可逆结合作用。其特征是抽搐张力最初降低,随后是张力增强期,最终导致张力降低至完全神经肌肉阻滞。通过评估类凝血酶毒素对终板电位幅度(EPP)的作用,进一步研究了其对肌肉张力的这些作用。这揭示了运动神经末梢乙酰胆碱神经诱发释放的类似三相改变。对乙酰胆碱释放的这些作用被证实是突触前起源的,因为微小终板电位(MEPPs)的模态幅度没有降低,并且在抽搐张力实验中,当神经诱发释放完全被阻断时,肌肉仍对直接肌肉刺激产生收缩反应。有趣的是,观察到类凝血酶毒素对乙酰胆碱的自发释放有显著影响,包括MEPP频率显著增加、MEPP幅度频率直方图向右偏移,以及由此导致的“巨型”MEPP数量增加。这些结果表明,类凝血酶毒素导致神经肌肉传递的突触前阻滞,涉及控制乙酰胆碱释放的调节机制的破坏。