Kharkevich D A, Fisenko V P
Arch Int Pharmacodyn Ther. 1981 Jun;251(2):255-69.
The comparative sensitivity of acetylcholine receptors of different skeletal muscles--m. masseter, m. gastrocnemius, m. triceps brachii, mm. obliquus et transversus abdominis, mm. intercostales, m. phrenicus to neuromuscular blocking agents was investigated. Experiments were performed on cats anesthetized with urethane (600 mg/kg, i.v.) and chloralose (70 mg/kg, i.v.). Muscle action potentials evoked by electrical stimulation of motor nerves were recorded. Derivatives of alpha-truxillic acid--anatruxonium and cyclobutonium, steroidal neuromuscular blocking agents--pancuronium and pipecurium, decamethonium and succinylcholine and their N-adamantyl analogues--decadonium and diadonium respectively, as well as tubocurarine chloride were tested. It was shown that the succession of relaxation of different skeletal muscles induced by the neuromuscular blocking agents of different chemical structure is variable.
研究了不同骨骼肌(咬肌、腓肠肌、肱三头肌、腹外斜肌和腹横肌、肋间肌、膈神经)的乙酰胆碱受体对神经肌肉阻滞剂的相对敏感性。实验在使用氨基甲酸乙酯(600mg/kg,静脉注射)和氯醛糖(70mg/kg,静脉注射)麻醉的猫身上进行。记录电刺激运动神经诱发的肌肉动作电位。测试了α-特鲁昔酸衍生物(阿那曲铵和环丁铵)、甾体类神经肌肉阻滞剂(泮库溴铵和哌库溴铵)、十烃季铵和琥珀酰胆碱及其N-金刚烷基类似物(分别为癸铵和二铵)以及氯化筒箭毒碱。结果表明,不同化学结构的神经肌肉阻滞剂引起的不同骨骼肌松弛顺序是可变的。