Martelle Jennifer L, Nader Michael A
Department of Physiology and Pharmacology, Wake Forest University School of Medicine, 546 NRC, Medical Center Boulevard, Winston-Salem, NC 27157-1083, USA.
Psychopharmacology (Berl). 2009 Apr;203(2):343-53. doi: 10.1007/s00213-008-1322-5. Epub 2008 Sep 21.
Drug discrimination (DD) and drug self-administration (SA) are frequently used preclinical assays. All preclinical studies with cocaine have examined the discriminative stimulus (S(D)) and reinforcing (S(R)) effects in separate groups of subjects.
The objective of the study is to train drug-naïve rhesus macaques to discriminate self-administered cocaine from saline and to assess S(D) and S(R) effects using a within-subjects design.
Adult male rhesus monkeys (n = 4) were trained to self-administer cocaine (0.1 mg/kg per injection) under a progressive-ratio (PR) reinforcement schedule. Next, they were trained to discriminate self-administered cocaine (0.45 or 0.56 mg/kg) or saline under a fixed-ratio (FR) 50 schedule of food presentation. The final schedule combined DD and SA into a multiple [chained FR 50 SA (cocaine or saline), food-reinforced DD] and PR SA schedule.
Each subject acquired SA under a PR schedule with significant differences in breakpoint between saline and cocaine evident by session 5. Self-administered cocaine was established as an S(D), such that 80% of responding before delivery of the first reinforcer and 90% of all responding occurred on the injection-appropriate lever. In all monkeys, there was at least one cocaine dose that did not engender cocaine-appropriate responding during DD (i.e., <20% cocaine-appropriate responding) yet functioned as a reinforcer during PR SA, suggesting that cocaine-like S(D) effects are not necessary for cocaine reinforcement.
This within-subject model may provide new information related to the behavioral mechanisms of action leading to the high abuse potential of cocaine; such information may lead to novel pharmacological treatment strategies for addiction.
药物辨别(DD)和药物自我给药(SA)是常用的临床前试验。所有关于可卡因的临床前研究都在不同组的受试者中分别研究了辨别刺激(S(D))和强化(S(R))作用。
本研究的目的是训练未接触过药物的恒河猴将自我给药的可卡因与生理盐水区分开来,并使用受试者内设计评估S(D)和S(R)作用。
成年雄性恒河猴(n = 4)在累进比率(PR)强化程序下接受训练,自我给药可卡因(每次注射0.1 mg/kg)。接下来,它们在固定比率(FR)50的食物呈现程序下接受训练,以辨别自我给药的可卡因(0.45或0.56 mg/kg)或生理盐水。最终程序将DD和SA组合成一个多重[连锁FR 50 SA(可卡因或生理盐水),食物强化DD]和PR SA程序。
每只受试者在PR程序下获得了SA,到第5次试验时,生理盐水和可卡因之间的断点有显著差异。自我给药的可卡因被确立为一种S(D),使得在第一次强化物发放前80%的反应以及所有反应的90%发生在与注射相应的杠杆上。在所有猴子中,至少有一个可卡因剂量在DD期间没有引起与可卡因相应的反应(即<20%与可卡因相应的反应),但在PR SA期间起到了强化作用,这表明可卡因样的S(D)作用对于可卡因强化不是必需的。
这种受试者内模型可能提供与导致可卡因高滥用潜力的行为作用机制相关的新信息;此类信息可能会带来新的成瘾药物治疗策略。