目的探讨七氟醚增强非去极化肌松药肌松作用的机制。
Aim To investigate the mechanism of sevoflurane enhancement of muscle relaxation.
另外，非去极化肌松药还可以改变烟碱样受体的类脂膜，改变其离子通道。
In addition, non depolarizing neuromuscular blocking drugs may alter the lipid membrane around the nicotinic cholinergic receptors, changing the properties of the ion channel.
除了利多卡因以外，几乎所有的局麻药都对非去极化型肌松药产生这样的作用。
In addition to lidocaine, nearly all the local anesthetics have been shown to have this effect on neuromuscular blockade.
目的研究肌电图型强直后单爆发刺激（PTB）在监测深度非去极化阻滞中的作用。
Objective To study the feasibility of monitoring intense neuromuscular blockade (NMB) with post tetanic burst (PTB).
结论盐酸戊乙奎醚作为术前用药更适合仅使用非去极化肌肉松弛剂作为肌肉松弛诱导的全麻患者。
Conclusion Penehyclidine hydrochloride is a better premedicant choice for patients under general anesthesia induced by nondepolarizing muscle relaxant Atracurium.
在给琥珀胆碱前，先给一点次肌松剂量的非去极化神经肌肉阻滞剂，也可以防止琥珀酰胆碱所致的眼内压增加。
The prior administration of subparalyzing doses of nondepolarizing neuromuscular blocking drugs may also prevent succinylcholine-induced increases in intraocular pressure.
可以用非去极化的神经肌肉阻滞剂(如维可罗宁、卡肌宁或潘可罗宁)代替琥珀胆堿，但麻醉的出现将延迟60秒钟。
A non - depolarizing neuromuscular blocking drug (e. g., vecuronium, atracurium, or pancuronium) can be substituted for succinylcholine, but the onset of paralysis is delayed by about 60 seconds.
可以用非去极化的神经肌肉阻滞剂(如维可罗宁、卡肌宁或潘可罗宁)代替琥珀胆堿，但麻醉的出现将延迟60秒钟。
A non - depolarizing neuromuscular blocking drug (e. g., vecuronium, atracurium, or pancuronium) can be substituted for succinylcholine, but the onset of paralysis is delayed by about 60 seconds.
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