DISRUPTION OF TEMPORALLY ORGANIZED BEHAVIOR BY MORPHINE

• Published in: Journal of the experimental analysis of behavior 2002-03, Vol.77 (2), p.157-169
• Main Authors: Knealing, Todd W., Schaal, David W.
• Format: Article
• Language: English
• Subjects: Animal behavior; Animals; Appetitive Behavior - drug effects; Birds; Columbidae; Dose-Response Relationship, Drug; Experiments; fixed-interval schedules; key peck; Male; morphine; Morphine - pharmacology; Motivation; peak procedure; pigeons; Reaction Time - drug effects; Reinforcement Schedule; temporal discrimination; Time Perception - drug effects; timing
• ISSN: 0022-5002; 1938-3711
• DOI: 10.1901/jeab.2002.77-157

Four pigeons pecked keys in two different procedures commonly used in the study of timing, or temporal discrimination. Sessions consisted of 40 trials. During half of the trials, two keys were presented for 50 s. Left‐key pecks were reinforced according to a variable‐interval 67.86‐s schedule during the first 25 s of the trial, and right‐key pecks were not reinforced. During the second 25 s of the trial, right‐key pecks were reinforced according to the same schedule, and left‐key pecks were not reinforced. In the other half of the 40‐trial session, the center key was presented. The majority of these trials arranged fixed‐interval 25‐s schedules. Occasionally a probe, or peak‐interval, trial was presented. These trials were 100 s in duration and terminated without reinforcement. These two procedures were used to examine the effects of morphine on indexes of timing and on patterns of responding. Morphine altered behavior in a rate‐dependent manner in both procedures. Low baseline (saline) response rates were increased following morphine administration, and high baseline rates were either unaffected or decreased slightly. Rate‐dependent effects appeared as leftward shifts in the timing index for two‐key trials and decreases in the index of curvature for fixed‐interval trials. Despite large changes in response rates, no consistent shift of the peak time was observed during peak‐interval trials. These results are discussed primarily in terms of rate dependency; that is, rates of responding following drug administration tend to be determined in large part by rates of responding under baseline conditions.