Shuster L, Webster G W, Yu G
J Pharmacol Exp Ther. 1975 Jan;192(1):64-7.
The running response of B6AF1/J mice to 25 mg/kg of morphine sulfate was increased up to 3-fold when this dose was administered either twice daily for 5 days or once a week for 2 or 3 weeks. The effect of weekly pretreatment was proportional to the dose of morphine and lasted as long as 1 month after pretreatment was stopped. There was no sensitization when the mice were less than 15 days old at the time of pretreatment. Of the parental strains, untreated C57Bl/6J mice showed a good running response to morphine, while A/J mice showed little response. Pretreatment of either of these strains produced only slight sensitization. Pretreatment of the hybrids with levorphanol increased the response to morphine. Dextrorphan and naloxone were ineffective. Sensitization by morphine was blocked by naloxone. Increased morphine running was not associated with analgesic tolerance as measured by the tail-flick assay. Morphine pretreatment produced some increase in the running response to amphetamine and to cocaine. Pretreatment with amphetamine or cocaine did not increase the response to morphine.
当以25毫克/千克的硫酸吗啡剂量,每天给药两次,持续5天,或每周给药一次,持续2或3周时,B6AF1/J小鼠的跑步反应增加了两倍。每周预处理的效果与吗啡剂量成正比,且在停止预处理后长达1个月仍持续存在。预处理时小鼠小于15天大则不会出现敏化现象。在亲本品系中,未处理的C57Bl/6J小鼠对吗啡表现出良好的跑步反应,而A/J小鼠反应很小。对这两个品系中的任何一个进行预处理仅产生轻微的敏化。用左啡诺对杂种小鼠进行预处理可增加对吗啡的反应。右啡烷和纳洛酮无效。吗啡引起的敏化被纳洛酮阻断。通过甩尾试验测量,吗啡引起的跑步增加与镇痛耐受性无关。吗啡预处理使对苯丙胺和可卡因的跑步反应有所增加。用苯丙胺或可卡因预处理不会增加对吗啡的反应。