Sakaue Akiko, Honda Motoko, Tanabe Mitsuo, Ono Hideki
Laboratory of CNS Pharmacology, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Japan.
J Pharmacol Sci. 2004 Jun;95(2):181-8. doi: 10.1254/jphs.fpj03087x.
The effects of various sodium channel blocking agents on acute thermal and mechanical nociception, as assessed using the plantar and tail pressure tests, respectively, were compared with the effects of morphine. The drugs used were mexiletine, lidocaine, carbamazepine, phenytoin, eperisone, tolperisone, and zonisamide. The sodium channel blocking agents exhibited a rather preferential elevation of the threshold for thermal nociception. By contrast, morphine produced similar analgesic effects on thermal and mechanical nociception. In the sciatic nerve isolated from mice, mexiletine, lidocaine, eperisone, and tolperisone impaired the propagation of low frequency action potentials (evoked at 0.2 Hz). Carbamazepine, phenytoin, and zonisamide generated a more frequency-dependent local anesthetic action with their obvious effects on higher frequency action potentials (evoked at 5 and/or 10 Hz). Our results show that sodium channel blocking agents have a preferential antinociceptive action against thermal stimulation that is likely to be attributed to their local anesthetic action.
分别使用足底和尾部压力测试评估了各种钠通道阻滞剂对急性热痛觉和机械性痛觉的影响,并与吗啡的作用进行了比较。所用药物为美西律、利多卡因、卡马西平、苯妥英、乙哌立松、托哌酮和唑尼沙胺。钠通道阻滞剂对热痛觉阈值有相当程度的优先提高作用。相比之下,吗啡对热痛觉和机械性痛觉产生相似的镇痛作用。在从小鼠分离出的坐骨神经中,美西律、利多卡因、乙哌立松和托哌酮会损害低频动作电位(以0.2 Hz诱发)的传导。卡马西平、苯妥英和唑尼沙胺产生更依赖频率的局部麻醉作用,对更高频率的动作电位(以5和/或10 Hz诱发)有明显影响。我们的结果表明,钠通道阻滞剂对热刺激具有优先的抗伤害感受作用,这可能归因于它们的局部麻醉作用。