Smurthwaite S T, Riley A L
Department of Psychology, American University, Washington, DC 20016.
Pharmacol Biochem Behav. 1992 Nov;43(3):839-46. doi: 10.1016/0091-3057(92)90416-d.
Using the conditioned taste aversion baseline of drug discrimination learning, animals were trained to discriminate diprenorphine from distilled water. In subsequent generalization tests, the opiate antagonists naltrexone and naloxone and the mixed opiate agonist/antagonist nalorphine substituted for the diprenorphine stimulus in a dose-dependent manner, while the opiate agonist morphine and the nonopiate pentobarbital failed to substitute even at the highest doses tested. That a range of opiate antagonists substituted for the diprenorphine stimulus (and an opiate agonist and a nonopiate failed to substitute) suggest that diprenorphine's antagonist properties may mediate the discrimination, presumably by blocking endogenous opiate activity. The ability of these drugs to substitute for the diprenorphine stimulus may also be a function of this receptor activity. The differences in the specific generalization patterns reported in the present assessment and those of earlier reports were discussed.
利用药物辨别学习的条件性味觉厌恶基线,训练动物区分二丙诺啡和蒸馏水。在随后的泛化测试中,阿片类拮抗剂纳曲酮和纳洛酮以及混合阿片类激动剂/拮抗剂纳洛芬以剂量依赖的方式替代了二丙诺啡刺激,而阿片类激动剂吗啡和非阿片类的戊巴比妥即使在测试的最高剂量下也未能替代。一系列阿片类拮抗剂替代了二丙诺啡刺激(而一种阿片类激动剂和一种非阿片类未能替代),这表明二丙诺啡的拮抗剂特性可能介导了这种辨别,大概是通过阻断内源性阿片类活性。这些药物替代二丙诺啡刺激的能力也可能是这种受体活性的一种功能。讨论了本评估中报告的特定泛化模式与早期报告中的差异。