Petry N M, Heyman G M
Harvard University, USA.
J Exp Anal Behav. 1995 Nov;64(3):331-59. doi: 10.1901/jeab.1995.64-331.
These experiments examined the own-price and cross-price elasticities of a drug (ethanol mixed with 10% sucrose) and a nondrug (10% sucrose) reinforcer. Rats were presented with ethanol-sucrose and sucrose, both available on concurrent independent variable-ratio (VR) 8 schedules of reinforcement. In Experiment 1, the variable ratio for the ethanol mix was systematically raised to 10, 12, 14, 16, 20, and 30, while the variable ratio for sucrose remained at 8. Five of the 6 rats increased ethanol-reinforced responding at some of the increments and defended baseline levels of ethanol intake. However, the rats eventually ceased ethanol-reinforced responding at the highest variable ratios. Sucrose-reinforced responding was not systematically affected by the changes in variable ratio for ethanol mix. In Experiment 2, the variable ratio for sucrose was systematically increased while the ethanol-sucrose response requirement remained constant. The rats decreased sucrose-reinforced responding and increased ethanol-sucrose-reinforced responding, resulting in a two- to 10-fold increase in ethanol intake. Experiment 3 examined the substitutability of qualitatively identical reinforcers: 10% sucrose versus 10% sucrose. Increases in variable-ratio requirements at the preferred lever resulted in a switch in lever preference. Experiment 4 examined whether 10% ethanol mix substituted for 5% ethanol mix, with increasing variable-ratio requirements of the 5% ethanol. All rats eventually responded predominantly for the 10% ethanol mix, but total amount of ethanol consumed per session did not systematically change. In Experiment 5, the variable-ratio requirements for both ethanol and sucrose were simultaneously raised to VR 120; 7 of 8 rats increased ethanol-reinforced responding while decreasing sucrose-reinforced responding. These data suggest that, within this ethanol-induction procedure and within certain parameters, demand for ethanol-sucrose was relatively inelastic, and sucrose consumption was independent of ethanol-sucrose consumption. Demand for sucrose, on the other hand, was relatively elastic, and ethanol-sucrose readily substituted for it. The results are discussed in terms of applying a behavioral economic approach to relationships between drug and nondrug reinforcers.
这些实验研究了一种药物(乙醇与10%蔗糖混合)和一种非药物(10%蔗糖)强化物的自价格弹性和交叉价格弹性。给大鼠提供乙醇 - 蔗糖和蔗糖,二者均按照并发独立可变比率(VR)8强化程序可得。在实验1中,乙醇混合物的可变比率被系统地提高到10、12、14、16、20和30,而蔗糖的可变比率保持在8。6只大鼠中有5只在某些增量下增加了乙醇强化反应,并维持乙醇摄入量的基线水平。然而,在最高可变比率时,大鼠最终停止了乙醇强化反应。蔗糖强化反应并未因乙醇混合物可变比率的变化而受到系统性影响。在实验2中,蔗糖的可变比率被系统地提高,而乙醇 - 蔗糖的反应要求保持不变。大鼠减少了蔗糖强化反应,增加了乙醇 - 蔗糖强化反应,导致乙醇摄入量增加了2至10倍。实验3研究了质量相同的强化物之间的可替代性:10%蔗糖与10%蔗糖。在偏好杠杆处可变比率要求的增加导致杠杆偏好的转变。实验4研究了10%乙醇混合物是否能替代5%乙醇混合物,随着5%乙醇可变比率要求的增加。所有大鼠最终主要对10%乙醇混合物做出反应,但每次实验中乙醇的总消耗量没有系统性变化。在实验5中,乙醇和蔗糖的可变比率要求同时提高到VR 120;8只大鼠中有7只增加了乙醇强化反应,同时减少了蔗糖强化反应。这些数据表明,在这种乙醇诱导程序内且在某些参数范围内,对乙醇 - 蔗糖的需求相对缺乏弹性,蔗糖消耗与乙醇 - 蔗糖消耗无关。另一方面,对蔗糖的需求相对有弹性,乙醇 - 蔗糖很容易替代它。将从应用行为经济学方法研究药物与非药物强化物之间关系的角度来讨论这些结果。