Iorio L C, Deacon M A, Ryan E A
J Pharmacol Exp Ther. 1975 Jan;192(1):58-63.
A dose regimen for administration of morphine, test drugs with potential to cause physical dependence and naloxone was determined to allow within one experimental day acquisition of morphine-dependent mice and evaluation of the narcotic drugs for their ability to prevent naloxone-precipitated jumping. This test procedure can be used to assess capacity of unknown drugs to suppress morphine withdrawal symptoms; the mechanism of suppression can be subsequently determined in secondary tests. However, for known morphine-like analgesics, the test procedure appears to reliably assess physical dependence properties. The results obtained on subcutaneous administration of five selected narcotic drugs and apomorphine show that their order of potency was methadone greater than meperidine equal apomorphine greater than d-propoxyphene greater than pentazocine. Codeine, also tested subcutaneously, did not substitute at sublethal doses. Except for apomorphine, which might have masked naloxone-precipitated jumping by inducing behavioral aggression, the order of potency compares favorably with the degree of physical dependence reported in humans. Thus, the described procedure might be employed to evaluate morphine substitution and hence potential physical dependence liability of unknown narcotic-like analgesics.
确定了吗啡、具有导致身体依赖潜力的受试药物和纳洛酮的给药方案,以便在一个实验日内获得吗啡依赖小鼠,并评估麻醉药物预防纳洛酮诱发跳跃的能力。该测试程序可用于评估未知药物抑制吗啡戒断症状的能力;随后可在二次试验中确定抑制机制。然而,对于已知的吗啡样镇痛药,该测试程序似乎能可靠地评估身体依赖特性。对五种选定麻醉药物和阿扑吗啡皮下给药的结果表明,它们的效力顺序为美沙酮大于哌替啶等于阿扑吗啡大于右旋丙氧芬大于喷他佐辛。皮下给药测试的可待因在亚致死剂量下不能替代。除了阿扑吗啡可能通过诱发行为攻击掩盖了纳洛酮诱发的跳跃外,效力顺序与人类报告的身体依赖程度相符。因此,所描述的程序可用于评估吗啡替代情况,从而评估未知麻醉样镇痛药潜在的身体依赖倾向。