Mishra Y, Ramzan I
Pharmacy Department, University of Sydney, New South Wales, Australia.
Anesth Analg. 1993 Oct;77(4):780-3. doi: 10.1213/00000539-199310000-00022.
The effect of histamine 2-antagonist famotidine on neuromuscular paralysis induced with either nondepolarizing or depolarizing neuromuscular blocking drugs was examined in anesthetized and mechanically ventilated rats. Neuromuscular paralysis, as judged by tibialis anterior muscle twitch tension in response to sciatic nerve stimulation, was maintained at about 50% with intravenous bolus and infusion regimens of either atracurium, gallamine, succinylcholine, or decamethonium. Famotidine, 0.1, 1, and 4 mg/kg, intravenously, were then administered at 5-min intervals as the infusion of the neuromuscular blocker was continued. Famotidine at any of these three doses failed to alter the steady state neuromuscular paralysis produced with either atracurium (prefamotidine versus final postfamotidine paralysis (mean +/- SE depression of twitch tension, n = 6, 49.8 +/- 2.8 vs 51.5 +/- 2.6%), gallamine (47.8 +/- 1.6 vs 47.6 +/- 3.0%), succinylcholine (49.2 +/- 1.8 vs 49.4 +/- 2.0%), or decamethonium (50.3 +/- 2.1 vs 51.5 +/- 2.0%). Intravenous famotidine at human therapeutic doses, fails to alter neuromuscular function in vivo in rats.
在麻醉并机械通气的大鼠中,研究了组胺2拮抗剂法莫替丁对非去极化或去极化神经肌肉阻滞剂所致神经肌肉麻痹的影响。通过对坐骨神经刺激时胫前肌抽搐张力判断神经肌肉麻痹,使用阿曲库铵、加拉明、琥珀酰胆碱或十烃季铵的静脉推注和输注方案将其维持在约50%。然后在继续输注神经肌肉阻滞剂的同时,每隔5分钟静脉注射0.1、1和4mg/kg的法莫替丁。这三种剂量的法莫替丁均未能改变由阿曲库铵(法莫替丁给药前与给药后最终神经肌肉麻痹情况(抽搐张力降低的平均值±标准误,n = 6,49.8±2.8% 对 51.5±2.6%))、加拉明(47.8±1.6% 对 47.6±3.0%)、琥珀酰胆碱(49.2±1.8% 对 49.4±2.0%)或十烃季铵(50.3±2.1% 对 51.5±2.0%)所产生的稳态神经肌肉麻痹。人治疗剂量的静脉注射法莫替丁不会改变大鼠体内的神经肌肉功能。