Lee C, Yang E, Katz R L
Anesthesiology. 1978 May;48(5):311-4. doi: 10.1097/00000542-197805000-00002.
Interactions of neuromuscular effects of edrophonium, alpha-bungarotoxin, and beta-bungarotoxin were studied in 12 chickens using the sciatic-gastrocnemius nerve-muscle preparation to elucidate the mechanism of action of each drug. Modification by the toxins of neuromuscular effects of edrophonium depended on the level of block pre-established by the toxins. Edrophonium-induced augmentation of muscle twitch ("facilitation") was decreased by both toxins. As the block reached 50 per cent, the facilitation was nearly abolished. Edrophonium-induced contracture of the muscle was blocked by alpha-bungarotoxin only. At 25 per cent block, it was no longer observable in five of six preparations. Beta-bungarotoxin enhanced the contracture. At complete block, the contracture reached 156 (SE 11, n = 6) per cent of control. The authors conclude that edrophonium facilitates neuromuscular transmission by a prejunctional mechanism and causes contracture of the chicken muscle by a post-junctional activation. The beta-bungarotoxin-blocked nerve-muscle preparation of the chicken is a model of acute denervation potentially useful for the study of drug effects on the postjunctional membrane.
使用坐骨神经-腓肠肌神经肌肉标本,在12只鸡身上研究了依酚氯铵、α-银环蛇毒素和β-银环蛇毒素的神经肌肉效应相互作用,以阐明每种药物的作用机制。毒素对依酚氯铵神经肌肉效应的影响取决于毒素预先建立的阻断水平。两种毒素均降低了依酚氯铵诱导的肌肉抽搐增强(“易化”)。当阻断达到50%时,易化几乎完全消失。依酚氯铵诱导的肌肉挛缩仅被α-银环蛇毒素阻断。在25%的阻断率时,6个标本中有5个不再观察到挛缩。β-银环蛇毒素增强了挛缩。在完全阻断时,挛缩达到对照的156(标准误11,n = 6)%。作者得出结论,依酚氯铵通过节前机制促进神经肌肉传递,并通过节后激活导致鸡肌肉挛缩。鸡的β-银环蛇毒素阻断的神经肌肉标本是急性去神经的模型,可能有助于研究药物对节后膜的作用。