Zetler G
Pharmacology. 1982;25(3):121-9. doi: 10.1159/000137733.
The antinociceptive effect in mice (hot-plate test) of caerulein (0.15 mg/kg s.c.) was many times more resistant to naloxone than that of morphine (2 mg/kg s.c., equipotent with the caerulein dose). The ED50 (mg/kg s.c.) of naloxone (given simultaneously with an agonist) was with morphine 0.01 and with caerulein 0.07. When administered intravenously after the agonist, the ED50 (mg/kg i.v.) against morphine was 0.012 and that against caerulein was 0.62. In either type of experiment the dose-response lines of naloxone against caerulein were very shallow as compared with those against morphine. A caerulein dose of 5 micrograms/kg enhanced the antinociceptive effect of morphine only when given before morphine, but not when given after it. The limited additivity of the effects together with the different susceptibility to naloxone of the antinociceptive actions indirectly suggest that caerulein and morphine do not share the same mechanism of action. Palpebral ptosis occurred only after caerulein and was completely resistant to naloxone 8 mg/kg s.c.
蛙皮素(0.15毫克/千克,皮下注射)对小鼠的镇痛作用(热板试验)比吗啡(2毫克/千克,皮下注射,与蛙皮素剂量等效)对纳洛酮的耐药性强很多倍。纳洛酮(与激动剂同时给药)的半数有效量(毫克/千克,皮下注射),与吗啡合用为0.01,与蛙皮素合用为0.07。在激动剂给药后静脉注射时,纳洛酮对抗吗啡的半数有效量(毫克/千克,静脉注射)为0.012,对抗蛙皮素的为0.62。在任何一种实验类型中,与对抗吗啡相比,纳洛酮对抗蛙皮素的剂量-反应曲线都非常平缓。5微克/千克的蛙皮素剂量仅在吗啡给药前给予时增强吗啡的镇痛作用,而在吗啡给药后给予则无此作用。作用的有限相加性以及镇痛作用对纳洛酮的不同敏感性间接表明,蛙皮素和吗啡的作用机制不同。睑下垂仅在蛙皮素给药后出现,并且对8毫克/千克皮下注射的纳洛酮完全耐受。