Alcohol and Drug Abuse Research Center, McLean Hospital and Harvard Medical School, Belmont, MA 02478, USA.
J Exp Anal Behav. 2013 Mar;99(2):211-33. doi: 10.1002/jeab.15. Epub 2013 Jan 14.
We have adapted a nonhuman primate model of cocaine versus food choice to the rat species. To evaluate the procedure, we tested cocaine versus food choice under a variety of environmental manipulations as well as pharmacological pretreatments. Complete cocaine-choice dose-effect curves (0-1.0 mg/kg/infusion) were obtained for each condition under concurrent fixed ratio schedules of reinforcement. Percentage of responding emitted on the cocaine-reinforced lever was not affected significantly by removal of cocaine-associated visual or auditory cues, but it was decreased after removal of response-contingent or response-independent cocaine infusions. Cocaine choice was sensitive to the magnitude and fixed ratio requirement of both the cocaine and food reinforcers. We also tested the effects of acute (0.32, 0.56, 1.0, 1.8 mg/kg) and chronic (0.1, 0.32 mg/kg/hr) d-amphetamine treatment on cocaine choice. Acute and chronic d-amphetamine had opposite effects, with acute increasing and chronic decreasing cocaine choice, similar to observations in humans and in nonhuman primates. The results suggest feasibility and utility of the choice procedure in rats and support its comparability to similar procedures used in humans and monkeys.
我们已经将可卡因与食物选择的非人灵长类动物模型适应于大鼠物种。为了评估该程序,我们在各种环境操作以及药理学预处理下测试了可卡因与食物选择。在同时进行的固定比率强化计划下,对于每种条件,都获得了完整的可卡因选择剂量效应曲线(0-1.0mg/kg/输注)。可卡因强化杆上的反应频率不受去除可卡因相关的视觉或听觉线索的显著影响,但在去除与反应相关或无关的可卡因输注后,反应频率会降低。可卡因选择对可卡因和食物强化剂的大小和固定比率要求均敏感。我们还测试了急性(0.32、0.56、1.0、1.8mg/kg)和慢性(0.1、0.32mg/kg/hr)安非他命治疗对可卡因选择的影响。急性和慢性安非他命具有相反的作用,急性增加而慢性降低可卡因选择,这与人类和非人类灵长类动物的观察结果相似。结果表明该选择程序在大鼠中的可行性和实用性,并支持其与人类和猴子中使用的类似程序的可比性。