Weiss Stanley J, Kearns David N, Cohn Scott I, Schindler Charles W, Panlilio Leigh V
Department of Psychology, American University, Washington, DC 20016, USA.
J Exp Anal Behav. 2003 Jan;79(1):111-35. doi: 10.1901/jeab.2003.79-111.
Environmental stimuli that set the occasion wherein drugs are acquired can "trigger" drug-related behavior. Investigating the stimulus control of drug self-administration in laboratory animals should help us better understand this aspect of human drug abuse. Stimulus control of cocaine self-administration was generated here for the first time using multiple and chained schedules with short, frequently-alternating components--like those typically used to study food-maintained responding. The procedures and results are presented along with case histories to illustrate the strategies used to produce this stimulus control. All these multicomponent schedules contained variable-interval (VI) components as well as differential-reinforcement-of-other-behavior (DRO) or extinction components. Schedule parameters and unit dose were adjusted for each rat to produce stable, moderate rates in VI components, with minimal postreinforcement (infusion) pausing, and response cessation in extinction and DRO components. Whole-body drug levels on terminal baselines calculated retrospectively revealed that all rats maintained fairly stable drug levels (mean, 2.3 to 3.4 mg/kg) and molar rates of intake (approximately 6.0 mg/kg/hr). Within this range, no relation between local VI response rates and drug level was found. The stimulus control revealed in cumulative records was indistinguishable from that achieved with food under these schedules, suggesting that common mechanisms may underlie the control of cocaine- and food-maintained behavior.
促使获取毒品的环境刺激能够“触发”与毒品相关的行为。在实验动物中研究药物自我给药的刺激控制,应有助于我们更好地理解人类药物滥用的这一方面。本文首次使用具有短且频繁交替成分的多重和连锁时间表来产生可卡因自我给药的刺激控制,这些成分类似于通常用于研究食物维持反应的成分。现将程序和结果以及案例历史呈现出来,以说明用于产生这种刺激控制的策略。所有这些多成分时间表都包含可变间隔(VI)成分以及对其他行为的差别强化(DRO)或消退成分。针对每只大鼠调整时间表参数和单位剂量,以在VI成分中产生稳定、适度的反应率,使强化后(注射)停顿最小化,并在消退和DRO成分中使反应停止。回顾性计算的终末基线时的全身药物水平显示,所有大鼠的药物水平相当稳定(平均为2.3至3.4毫克/千克),摄入摩尔率(约6.0毫克/千克/小时)。在此范围内,未发现局部VI反应率与药物水平之间存在关联。累积记录中显示的刺激控制与在这些时间表下对食物所实现的刺激控制无法区分,这表明可卡因维持行为和食物维持行为的控制可能存在共同机制。