Romandini S, Samanin R
Psychopharmacology (Berl). 1984;82(1-2):140-2. doi: 10.1007/BF00426398.
A single subcutaneous injection of 5 mg/kg metergoline or 10 mg/kg methysergide, two serotonin antagonists, or 1 mg/kg naloxone, significantly reduced the effect of a subcutaneous dose of 3 mg/kg morphine in the tail immersion test in rats. The same drugs and doses were administered concurrently with 10 mg/kg morphine twice daily for 3 days and nociceptive responses were measured 96 h later. Tolerance to the effect of 3 mg/kg morphine was comparable in animals which had received vehicle + morphine or serotonin antagonists + morphine, whereas naloxone completely prevented the development of tolerance. The results argue against a role of serotonin in the development of tolerance to the antinociceptive effect of morphine and suggest it may be possible to dissociate morphine analgesia from tolerance development, at least in the conditions used in the present study.
单次皮下注射5毫克/千克的美替拉酮或10毫克/千克的甲基麦角新碱(两种5-羟色胺拮抗剂),或1毫克/千克的纳洛酮,可显著降低皮下注射3毫克/千克吗啡对大鼠尾部浸没法试验的影响。相同的药物和剂量与10毫克/千克吗啡同时每日两次给药,持续3天,并在96小时后测量伤害性反应。接受溶剂+吗啡或5-羟色胺拮抗剂+吗啡的动物对3毫克/千克吗啡作用的耐受性相当,而纳洛酮则完全阻止了耐受性的发展。结果表明5-羟色胺在吗啡抗伤害感受作用耐受性的发展中不起作用,并表明至少在本研究使用的条件下,有可能将吗啡镇痛与耐受性发展分离。