Czachowski C L, Samson H H, Denning C E
Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157-1083, USA.
Alcohol Clin Exp Res. 1999 Mar;23(3):398-403.
Assessment of drug effects on two different reinforcers at the same time requires that each reinforcer be sampled at approximately the same time. One procedure that effectively produces this result is the use of a multiple schedule of reinforcement in which two different reinforcers are presented in alternating 2-min components. In our study, sucrose and ethanol solutions were made available after appropriate lever-press responding. Subjects were trained to self-administer 10% ethanol using a sucrose-substitution procedure and to discriminate light cues associated with the different reinforcers until stable reinforcer-directed responding was achieved on both the ethanol- and the sucrose-associated lever during the changing 2-min components of the schedule. Subsequently, the reinforcer solution presented on one lever was held constant while the concentration of the alternate reinforcer was manipulated, i.e., ethanol concentrations of 0 to 15% and sucrose concentrations of 0 to 10% were assessed. This multiple schedule procedure resulted in sustained and independent ethanol- and sucrose-reinforced behavior. Manipulation of the characteristics of one reinforcer had no effect on behavior maintained by the alternate reinforcer. Increases in sucrose concentration resulted in increases in sucrose-directed responding with no change in ethanol responding, and increases in ethanol concentration resulted in increases in ethanol intake with no change in sucrose responding. Our methods can be used to examine differential drug effects on ethanol- and sucrose-reinforced behavior in the same animal over a single time course without the confounds or interference from the concurrently available reinforcer.
同时评估药物对两种不同强化物的作用要求在大致相同的时间对每种强化物进行采样。一种有效产生此结果的程序是使用多重强化程序,其中两种不同的强化物在交替的2分钟时间段内呈现。在我们的研究中,在适当的杠杆按压反应后提供蔗糖和乙醇溶液。使用蔗糖替代程序训练受试者自我给药10%的乙醇,并辨别与不同强化物相关的光信号,直到在程序变化的2分钟时间段内,在与乙醇和蔗糖相关的杠杆上都实现稳定的强化物导向反应。随后,保持一个杠杆上呈现的强化物溶液不变,同时操纵另一种强化物的浓度,即评估0%至15%的乙醇浓度和0%至10%的蔗糖浓度。这种多重程序导致持续且独立的乙醇和蔗糖强化行为。一种强化物特征的操纵对由另一种强化物维持的行为没有影响。蔗糖浓度的增加导致蔗糖导向反应增加,而乙醇反应无变化;乙醇浓度的增加导致乙醇摄入量增加,而蔗糖反应无变化。我们的方法可用于在单个时间进程中检查同一动物中药物对乙醇和蔗糖强化行为的不同影响,而不会受到同时存在的强化物的混淆或干扰。