TAVERNER D
Br J Pharmacol Chemother. 1960 Mar;15(1):201-6. doi: 10.1111/j.1476-5381.1960.tb01231.x.
The effects of intravenously injected lignocaine, procaine and amethocaine on the monosynaptic and polysynaptic reflexes and the cord dorsum potentials elicited by selective electrical stimulation of appropriate afferent fibres have been investigated in decerebrate cats before and after strychnine. The three drugs depress the amplitude of the reflex responses in the basal preparation for 40 to 50 min. Smaller doses eliminate the reflex augmentation produced by strychnine for comparable periods. Very small doses selectively abolish the augmentation of the P component of the cord dorsum response induced by strychnine. The drugs have no effect on post-tetanic potentiation of the monosynaptic reflex response evoked from the gastrocnemius muscle in the cat. Their activity on the spinal cord is roughly proportional to their local anaesthetic potency. The ratios of the doses which produce the same central activity are amethocaine 3: lignocaine 10: procaine 20.
在士的宁处理前后的去大脑猫中,研究了静脉注射利多卡因、普鲁卡因和丁卡因对单突触和多突触反射以及通过选择性电刺激适当传入纤维所引发的脊髓背根电位的影响。在基础准备状态下,这三种药物可使反射反应的幅度降低40至50分钟。较小剂量可在相当长的时间内消除士的宁引起的反射增强。极小剂量可选择性地消除士的宁诱导的脊髓背根反应P成分的增强。这些药物对猫腓肠肌诱发的单突触反射反应的强直后增强没有影响。它们对脊髓的作用大致与其局部麻醉效力成正比。产生相同中枢作用的剂量比为丁卡因3:利多卡因10:普鲁卡因20。