Nabeshima T, Yamada S, Yamaguchi K, Matsuno K, Kameyama T, Sakakibara S, Matsumoto S
Nihon Yakurigaku Zasshi. 1983 May;81(5):411-20.
It was investigated whether the analgesic effects of eptazocine were antagonized by treatment with naloxone, one of the opiate antagonists, and whether morphine-induced effects were affected by eptazocine. The analgesic effects of eptazocine, similar to those of morphine, were completely antagonized by treatment with 0.5 mg/kg naloxone, s.c., as determined by the hot plate and pressure methods in mice and by the tail-flick method in rats. In contrast, as tested by the acetic acid-induced writhing method in mice, the analgesic effect of eptazocine, similar to that of pentazocine, was not antagonized by treatment with 1.0 mg/kg naloxone, s.c., while that of morphine was antagonized by 0.5 mg/kg naloxone, s.c. Using the acetic acid-induced writhing method in mice, the pA2 values of naloxone were found to be the following order: eptazocine less than pentazocine less than morphine. In addition, the analgesic effect of morphine was dose-dependently antagonized by the treatment with eptazocine as determined by the pressure method. Furthermore, the stimulating effect of morphine on spontaneous locomotor activity was also antagonized by eptazocine. These results suggest that eptazocine may be classified as one of the opiate agonist-antagonists.
研究了纳洛酮(一种阿片拮抗剂)治疗是否会拮抗依他佐辛的镇痛作用,以及依他佐辛是否会影响吗啡诱导的效应。依他佐辛的镇痛作用与吗啡相似,通过小鼠热板法和压力法以及大鼠甩尾法测定,皮下注射0.5mg/kg纳洛酮可完全拮抗其镇痛作用。相比之下,通过小鼠醋酸诱导扭体法测试,皮下注射1.0mg/kg纳洛酮不会拮抗依他佐辛的镇痛作用(依他佐辛的镇痛作用与喷他佐辛相似),而皮下注射0.5mg/kg纳洛酮可拮抗吗啡的镇痛作用。使用小鼠醋酸诱导扭体法,发现纳洛酮的pA2值顺序如下:依他佐辛<喷他佐辛<吗啡。此外,通过压力法测定,依他佐辛治疗可剂量依赖性地拮抗吗啡的镇痛作用。此外,依他佐辛还可拮抗吗啡对自发运动活动的刺激作用。这些结果表明,依他佐辛可能可归类为阿片类激动剂-拮抗剂之一。