Pharmacology Department, Reckitt & Colman Limited, Dansom Lane, Hull.
Br J Clin Pharmacol. 1974 Jun;1(3):217-22. doi: 10.1111/j.1365-2125.1974.tb00239.x.
1 The effect of RX 72601, neostigmine plus atropine, or saline on neuromuscular blockade with (+)-tubocurarine was studied in a double blind trial in four healthy male volunteers. 2 The methods used to assess neuromuscular function were voluntary grip strength and indirectly evoked muscle twitches. The muscarinic action was assessed by measuring intestinal motility with a pressure sensitive radio pill, and auscultation of the abdomen. Blood pressure and pulse rate were also recorded. The degree of acetylcholinesterase inhibition achieved in whole blood was determined before and at intervals after the administration of the anticholinesterases. 3 Both RX 72601 (0.66-0.83 mg) and neostigmine (2.5 mg) completely reversed the neuromuscular blockade produced by tubocurarine, but the time course of reversal differed. RX 72601 (0.66-0.83 mg) produced similar inhibition of acetylcholinesterase in whole blood to neostigmine (2.5 mg). The doses of RX 72601 used caused minimal stimulation at muscarinic sites as evidenced by the limited effect on pulse rate and intestinal activity. 4 It was concluded that RX 72601 could be safely used to reverse the effects of neuromuscular blockade without the need for premedication with atropine.
1 在四项健康男性志愿者的双盲试验中,研究了 RX 72601、新斯的明加阿托品或生理盐水对(+)-筒箭毒碱引起的神经肌肉阻滞的影响。2 用于评估神经肌肉功能的方法是自愿握力和间接诱发的肌肉抽搐。通过使用压力敏感无线电丸测量肠道蠕动和听诊腹部来评估毒蕈碱作用。还记录了血压和脉搏率。在给予抗胆碱酯酶前后的不同时间点测定全血中乙酰胆碱酯酶的抑制程度。3 RX 72601(0.66-0.83mg)和新斯的明(2.5mg)均完全逆转了筒箭毒碱引起的神经肌肉阻滞,但逆转的时间过程不同。RX 72601(0.66-0.83mg)在全血中产生与新斯的明(2.5mg)相似的乙酰胆碱酯酶抑制作用。所使用的 RX 72601 剂量引起毒蕈碱部位的最小刺激,这从对脉搏率和肠道活动的有限影响中可以看出。4 结论是,RX 72601 可安全用于逆转神经肌肉阻滞的作用,而无需预先使用阿托品。