Foong F W, Satoh M, Takagi H
Arch Int Pharmacodyn Ther. 1982 Apr;256(2):212-8.
Effects of cyclazocine on the evoked-potentials at the trigeminal subnucleus caudalis, nucleus ventralis posteromedialis of the thalamus, somatosensory S1 area of the cerebral cortex and dorsal hippocampus following electrical stimulation of the tooth-pulp were studied using the rabbit. Pentazocine and morphine were used as reference drugs. Cyclazocine in doses of 0.5-1.0 mg/kg, i.v., significantly suppressed the evoked-potential recorded at the dorsal hippocampus but not those at the other sites. The hippocampal evoked-potential was significantly inhibited also by pentazocine (5.0-10 mg/kg, i.v.) and morphine (2.0-4.0 mg/kg, i.v.). The latter but not the former significantly depressed the evoked-potential at the S1 area of the cerebral cortex. The evoked-potential at the trigeminal subnucleus caudalis was not affected by these three drugs in the doses indicated. These results suggest that cyclazocine as well as pentazocine and morphine inhibit the electrically induced painful impulses at the hippocampus and/or the afferent pathways to the hippocampus from the trigeminal subnucleus caudalis such as the tooth-pulp-hypothalamo-hippocampal pathway.
采用家兔研究了环唑辛对牙髓电刺激后三叉神经尾侧亚核、丘脑腹后内侧核、大脑皮质体感S1区和背侧海马诱发电位的影响。喷他佐辛和吗啡用作参比药物。静脉注射剂量为0.5 - 1.0mg/kg的环唑辛可显著抑制背侧海马记录的诱发电位,但对其他部位的诱发电位无影响。静脉注射喷他佐辛(5.0 - 10mg/kg)和吗啡(2.0 - 4.0mg/kg)也可显著抑制海马诱发电位。吗啡而非喷他佐辛可显著降低大脑皮质S1区的诱发电位。三叉神经尾侧亚核的诱发电位不受这三种药物上述剂量的影响。这些结果表明,环唑辛以及喷他佐辛和吗啡可抑制海马处电诱导的疼痛冲动和/或从三叉神经尾侧亚核到海马的传入通路,如牙髓 - 下丘脑 - 海马通路。