Kameyama T, Nabeshima T, Yamaguchi K, Ukai M, Okuyama S, Sakakibara S
Nihon Yakurigaku Zasshi. 1981 Dec;78(6):599-612. doi: 10.1254/fpj.78.599.
The relationship between the analgesic action of eptazocine and brain catecholamine was investigated by pharmacological and neurochemical methods in comparison with pentazocine (PZC) and morphine (MOR). The analgesic action of eptazocine as determined by the pressure method was decreased by pretreatment with 6-hydroxydopamine (6-OHDA) or disulifram. Eptazocine increased the norepinephrine (NE)level in the brain stem, but decreased the dopamine (DA) level in the cortex. Eptazocine decreased the rates of DA turnover in the cortex and the brain stem and NE turnover in the spinal cord. The analgesic action of PZC was decreased by alpha-methyl-rho-tyrosine ( alpha-MT), disulfiram, 6-OHDA, or reserpine. PZC decreased NE levels in the cortex and the brain stem, and DA level in the striatum. The turnover rates of NE in the brain stem and the spinal cord were increased by PZC. The analgesic action of MOR was potentiated by alpha-MT and attenuated by reserpine or 6-OHDA. MOR decreased NE and DA levels in the cortex and NE level in the brain stem, but increased DA level in the brain stem and NE level in the spinal cord. The turnover rates of NE in the cortex and the brain stem were increased at low doses of MOR, but those of DA in the striatum and NE in the spinal cord were decreased at high dose of MOR. These results suggest that the mechanism of eptazocine-induced analgesia is different from those of PZC and MOR in terms of the relationship to catecholamine neurons.
通过药理学和神经化学方法,以喷他佐辛(PZC)和吗啡(MOR)作为对照,研究了依他佐辛的镇痛作用与脑内儿茶酚胺之间的关系。用6-羟基多巴胺(6-OHDA)或双硫仑预处理后,依他佐辛通过压力法测定的镇痛作用降低。依他佐辛可增加脑干中去甲肾上腺素(NE)水平,但降低皮质中多巴胺(DA)水平。依他佐辛降低了皮质和脑干中DA的周转速率以及脊髓中NE的周转速率。PZC的镇痛作用可被α-甲基对酪氨酸(α-MT)、双硫仑、6-OHDA或利血平降低。PZC降低了皮质和脑干中的NE水平以及纹状体中的DA水平。PZC增加了脑干和脊髓中NE的周转速率。MOR的镇痛作用被α-MT增强,被利血平或6-OHDA减弱。MOR降低了皮质中NE和DA水平以及脑干中NE水平,但增加了脑干中DA水平和脊髓中NE水平。低剂量MOR时,皮质和脑干中NE的周转速率增加,但高剂量MOR时,纹状体中DA和脊髓中NE的周转速率降低。这些结果表明,就与儿茶酚胺能神经元的关系而言,依他佐辛诱导镇痛的机制不同于PZC和MOR。