Kurachi M, Aihara H
Jpn J Pharmacol. 1984 Sep;36(1):7-13. doi: 10.1254/jjp.36.7.
The effects of chlorphenesin carbamate (CPC) and mephenesin on spinal neurons were investigated in spinal rats. CPC (50 mg/kg i.v.) inhibited the mono-(MSR) and poly-synaptic reflex (PSR), the latter being more susceptible than the former to CPC depression. Mephenesin also inhibited MSR and PSR, though the effects were short in duration. CPC had no effect on the dorsal root potential evoked by the stimulation of the dorsal root, while mephenesin reduced the dorsal root-dorsal root reflex. The excitability of motoneuron was reduced by the administration of CPC or mephenesin. The excitability of primary afferent terminal was unchanged by CPC, while it was inhibited by mephenesin. Neither CPC nor mephenesin influenced the field potential evoked by the dorsal root stimulation. Both CPC and mephenesin had no effect on the synaptic recovery. These results suggest that both CPC and mephenesin inhibit the firing of motoneurons by stabilizing the neuronal membrane, while mephenesin additionally suppresses the dorsal root reflex and the excitability of the primary afferent terminal. These inhibitory actions of CPC on spinal activities may contribute, at least partly, to its muscle relaxing action.
在脊髓大鼠中研究了氯苯甘醚(CPC)和美芬新对脊髓神经元的作用。CPC(静脉注射50mg/kg)抑制单突触反射(MSR)和多突触反射(PSR),后者比前者对CPC的抑制作用更敏感。美芬新也抑制MSR和PSR,但其作用持续时间较短。CPC对刺激背根诱发的背根电位没有影响,而美芬新降低了背根 - 背根反射。给予CPC或美芬新可降低运动神经元的兴奋性。CPC对初级传入终末的兴奋性没有影响,而美芬新可抑制其兴奋性。CPC和美芬新都不影响背根刺激诱发的场电位。CPC和美芬新对突触恢复均无影响。这些结果表明,CPC和美芬新都通过稳定神经元膜来抑制运动神经元的放电,而美芬新还额外抑制背根反射和初级传入终末的兴奋性。CPC对脊髓活动的这些抑制作用可能至少部分地促成了其肌肉松弛作用。