Fraser H F, Kay D C, Yeh S Y, Gorodetzky C W, Dewey W L
Drug Alcohol Depend. 1978 Sep;3(5):301-18. doi: 10.1016/0376-8716(78)90001-7.
When an opioid capable of forming active metabolites is administered, the total pharmacology is the result of interactions of the opioid and such metabolites, especially normetabolites. Normetabolites may affect the morphine-like characteristics of certain opioids and thus influence their reinforcement in animals and man. Most opioids, when administered in single doses, are positively reinforcing in addicts. Oral administration, as compared with parenteral, facilitates the formation of normetabolites. When chronically administered, many opioids, including acetylmethadol, meperidine, morphine, codeine, propoxyphene, and levorphanol, show evidence of a longer half-life for their normetabolites. Normetabolites may have aversive characteristics and thus impair positive reinforcement of the parent drug in animals and man. For example, addicts do not like chronic oral morphine or chronic oral codeine. Conversely, methadone, the normetabolites of which are inactive, is well accepted during chronic oral administration. Drugs which inhibit N-demethylation will increase the agonist potency of opioids having inactive normetabolites (e.g., methadone) but will decrease the agonist potency of opioids having more potent normetabolites than the parent (e.g., acetylmethadol). The divergent responses of addicts to single doses of opiates as compared with chronic doses indicate that chronic addiction tests in man are needed befored relative abuse liability can be predicted.
当给予一种能够形成活性代谢产物的阿片类药物时,其总的药理作用是该阿片类药物及其代谢产物(尤其是去甲基代谢产物)相互作用的结果。去甲基代谢产物可能会影响某些阿片类药物的吗啡样特性,从而影响它们在动物和人类中的强化作用。大多数阿片类药物单次给药时,对成瘾者具有正性强化作用。与胃肠外给药相比,口服给药有利于去甲基代谢产物的形成。当长期给药时,许多阿片类药物,包括醋美沙朵、哌替啶、吗啡、可待因、丙氧芬和左啡诺,其去甲基代谢产物的半衰期显示出延长的迹象。去甲基代谢产物可能具有厌恶特性,从而损害母体药物在动物和人类中的正性强化作用。例如,成瘾者不喜欢长期口服吗啡或长期口服可待因。相反,美沙酮的去甲基代谢产物无活性,在长期口服给药期间很容易被接受。抑制N-去甲基化的药物会增加去甲基代谢产物无活性的阿片类药物(如美沙酮)的激动剂效力,但会降低去甲基代谢产物比母体更有效的阿片类药物(如醋美沙朵)的激动剂效力。与长期剂量相比,成瘾者对单次剂量阿片类药物的不同反应表明,在预测相对滥用可能性之前,需要在人体中进行长期成瘾试验。