Koffarnus Mikhail N, Woods James H
Department of Psychology, University of Michigan, 1301 MSRB III, 1150 W Medical Center Dr., Ann Arbor, MI 48109, USA.
J Exp Anal Behav. 2008 Mar;89(2):209-24. doi: 10.1901/jeab.2008.89-209.
The generalized matching law provides precise descriptions of choice, but has not been used to characterize choice between different doses of drugs or different classes of drugs. The current study examined rhesus monkeys' drug self-administration choices between identical drug doses, different doses, different drugs (cocaine, remifentanil, and methohexital), and between drug and drug-paired stimuli. The bias parameter of the generalized matching law was used to quantify preference for one reinforcer over another. Choice between identical drug doses yielded undermatching. Choices between 0.3 microg/kg/injection remifentanil and either 0.1 microg/kg/injection remifentanil or saline plus drug-paired stimuli revealed bias for the 0.3 microg/kg/injection dose. Choice was relatively insensitive to differences in random interval schedule value when one reinforcer was replaced with drug-paired stimulus presentations. Bias for 0.3 microg/kg/injection remifentanil over 10 microg/kg/injection cocaine was seen in one subject, and indifference was generally observed between 0.1 microg/kg/injection remifentanil and 56 microg/kg/injection cocaine and between 30 microg/kg/injection cocaine and 320 microg/kg/injection methohexital. These findings suggest the bias parameter may be useful in quantitatively measuring level of preference, which would be an advantage over concurrent FR procedures that often result in exclusive choice.
广义匹配法则提供了对选择的精确描述,但尚未用于描述在不同剂量的药物或不同类别的药物之间的选择。当前的研究考察了恒河猴在相同药物剂量、不同剂量、不同药物(可卡因、瑞芬太尼和美索比妥)之间以及在药物与药物配对刺激之间的药物自我给药选择。广义匹配法则的偏差参数用于量化对一种强化物相对于另一种强化物的偏好。相同药物剂量之间的选择产生了不匹配。在0.3微克/千克/注射的瑞芬太尼与0.1微克/千克/注射的瑞芬太尼或生理盐水加药物配对刺激之间的选择显示出对0.3微克/千克/注射剂量的偏好。当一种强化物被药物配对刺激呈现所取代时,选择对随机间隔时间表值的差异相对不敏感。在一个受试者中观察到对0.3微克/千克/注射的瑞芬太尼相对于10微克/千克/注射的可卡因的偏好,并且在0.1微克/千克/注射的瑞芬太尼与56微克/千克/注射的可卡因之间以及在30微克/千克/注射的可卡因与320微克/千克/注射的美索比妥之间通常观察到无差异。这些发现表明偏差参数可能有助于定量测量偏好水平,这将是相对于经常导致排他性选择的同时固定比率程序的一个优势。