Behavioral mechanisms of oxycodone's effects in female and male rats: Reinforcement delay and impulsive choice.

μ-Opioid agonists (e.g., morphine) typically increase which has been interpreted as an opioid-induced increase in sensitivity to reinforcement delay.

A method for studying reinforcement factors controlling impulsive choice for use in behavioral neuroscience.

Although procedures originating within the experimental analysis of behavior commonly are used in behavioral neuroscience to produce behavioral endpoints, they are used less often to analyze the behavioral processes involved, particularly at the level of individual organisms (see Soto, 2020). Concurrent-chains procedures have been used extensively to study choice and to quantify relations between various dimensions of reinforcement and preference. Unfortunately, parametric analysis of those relations using traditional steady-state, single-subject experimental designs can be time-consuming, often rendering these procedures impractical for use in behavioral neuroscience.

Effects of chlordiazepoxide on pausing during rich-to-lean transitions.

Extended pausing during discriminable transitions from rich-to-lean conditions can be viewed as escape (i.e., rich-to-lean transitions function aversively).

Assessing functions of stimuli associated with rich-to-lean transitions using a choice procedure.

Under fixed-ratio schedules, transitions from more to less favorable conditions of reinforcement (rich-to-lean transitions) usually generate extended pausing. One possible explanation for this effect is that stimuli associated with rich-to-lean transitions are aversive and, thus, extended pausing functions as escape. The purpose of this study was to characterize further the aversive function of different transitions, and the stimuli associated with them, by allowing pigeons to choose to complete select ratios in the presence of either a mixed-schedule stimulus or a transition-specific multiple-schedule stimulus.