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DIFFERENTIAL EFFECTS OF COCAINE AND PENTOBARBITAL ON FIXED‐INTERVAL AND RANDOM‐INTERVAL PERFORMANCE
Author(s) -
Howell Leonard L.,
Byrd Larry D.,
Marr M. J.
Publication year - 1988
Publication title -
journal of the experimental analysis of behavior
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.75
H-Index - 61
eISSN - 1938-3711
pISSN - 0022-5002
DOI - 10.1901/jeab.1988.49-411
Subject(s) - pentobarbital , mathematics , interval (graph theory) , stimulus control , statistics , anesthesia , medicine , combinatorics , nicotine
Reports have indicated that the behavioral effects of a drug can be related to the nondrug control rate of behavior in the absence of the drug. To investigate the purported relationship between control rate and drug rate, squirrel monkeys were trained under a fixed‐interval 300‐s schedule of stimulus‐shock termination, a procedure that engendered a wide range of response rates. A light illuminated the experimental chamber during the fixed interval, and the first lever press after 300 s had elapsed terminated the light for 30 s and precluded an electrical stimulus to the tail. Following acute intra‐muscular administration of cocaine (0.03–0.56 mg/kg), overall rate increased and different control rates of responding, during different parts of the fixed interval, converged toward a common rate. Subsequently, the schedule was changed to a multiple fixed‐interval 300‐s random‐interval 300‐s schedule; performance during the random‐interval component was characterized by steady responding at a uniformly high rate. Analysis of fixed‐interval and random‐interval performances following acute cocaine administration revealed convergence of response rates toward a common, uniform rate. Pentobarbital (0.3–10.0 mg/kg) only decreased overall rate, and different control rates of responding during the fixed interval did not converge toward a common rate. The results indicate that this type of analysis can be useful in comparing pharmacological agents from different classes and that the rate at which responding becomes uniform can provide a quantitative behavioral end point for characterizing drug effects on behavior.