Snodgrass S H, Hardin J L, McMillan D E
Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock 72205, USA.
J Exp Anal Behav. 1997 Jul;68(1):117-32. doi: 10.1901/jeab.1997.68-117.
Four rats responded under a simple fixed consecutive number schedule in which eight or more consecutive responses on the run lever, followed by a single response on the reinforcement lever, produced the food reinforcer. Under this simple schedule, dose-response curves were determined for diazepam, morphine, pentobarbital, and phencyclidine. The rats were then trained to respond under a multiple fixed consecutive number schedule in which a discriminative stimulus signaled when the response requirement on the run lever had been completed in one of the two fixed consecutive number component schedules. Under control conditions, the percentage of reinforced runs under the multiple-schedule component with the discriminative stimulus added was much higher than the percentage of reinforced runs under the multiple-schedule component without the discriminative stimulus. All of the drugs decreased the percentage of reinforced runs under each of the fixed consecutive number schedules by increasing the conditional probability of short run lengths. This effect was most consistently produced by morphine. The drugs produced few differences in responding between the multiple fixed consecutive number components. Responding under the simple fixed consecutive number schedule, however, was affected at lower doses of the drugs than was responding under the same fixed consecutive number schedule when it was a component of the multiple schedule. This result may be due to the difference in schedule context or, perhaps, to the order of the experiments.
四只大鼠在简单固定连续数强化程序下做出反应,即奔跑杠杆上连续八次或更多次反应,接着在强化杠杆上单次反应,便可获得食物强化物。在此简单程序下,测定了地西泮、吗啡、戊巴比妥和苯环己哌啶的剂量反应曲线。然后训练大鼠在多重固定连续数强化程序下做出反应,其中当在两个固定连续数子强化程序之一中完成奔跑杠杆上的反应要求时,辨别性刺激会发出信号。在对照条件下,添加辨别性刺激的多重强化程序子程序下的强化奔跑百分比,远高于无辨别性刺激的多重强化程序子程序下的强化奔跑百分比。所有药物通过增加短奔跑长度的条件概率,降低了每个固定连续数强化程序下的强化奔跑百分比。这种效应在吗啡作用下最为一致。这些药物在多重固定连续数子程序之间的反应上几乎没有差异。然而,与在多重强化程序中作为一个子程序的相同固定连续数强化程序相比,在简单固定连续数强化程序下做出反应时,药物在较低剂量时就受到影响。这一结果可能是由于强化程序背景的差异,或者也许是由于实验顺序。