Dretchen K L, Morgenroth V H, Standaert F G, Walts L F
Anesthesiology. 1976 Dec;45(6):604-9.
The neuromuscular effects of azathioprine were examined in the in-vivo cat soleus muscle preparation. In concentrations ranging from 10 to 1,000 mug/kg, administered intra-arterially, the agent caused motor axons to fire repetitively and produced a dose-related increase in the force of contraction. The drug reversed neuromuscular blockage produced by d-tubocurarine and potentiated the neuromuscular blockade produced by succinylcholine. The effects of theophylline, a phosphodiesterase inhibitor, on neuromuscular transmission were identical to those produced by azathioprine. Using an in-vitro assay preparation, azathioprine was found to produce 50 per cent inhibition (IC50) of phosphodiesterase at a concentration of 2 X 10(-5) M. In the same preparation, theophylline had an IC50 of 1 X 10(-4) M. Neither agent in concentrations to 10(-2) M affected cholinesterase activity measured in vitro. It is concluded that the effects of azathioprine on neuromuscular transmission are due to inhibition of phosphodiesterase in the motor nerve terminal.
在活体猫比目鱼肌标本中研究了硫唑嘌呤的神经肌肉效应。动脉内给予浓度范围为10至1000微克/千克的该药物,可使运动轴突重复放电,并使收缩力产生剂量相关的增加。该药物可逆转由d - 筒箭毒碱引起的神经肌肉阻滞,并增强由琥珀酰胆碱引起的神经肌肉阻滞。磷酸二酯酶抑制剂茶碱对神经肌肉传递的作用与硫唑嘌呤产生的作用相同。使用体外测定制剂,发现硫唑嘌呤在浓度为2×10⁻⁵ M时可产生50%的磷酸二酯酶抑制作用(IC50)。在同一制剂中,茶碱的IC50为1×10⁻⁴ M。浓度达10⁻² M的两种药物均未影响体外测定的胆碱酯酶活性。得出的结论是,硫唑嘌呤对神经肌肉传递的作用是由于抑制了运动神经末梢中的磷酸二酯酶。