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The partial reinforcement extinction effect after treatment with chlordiazepoxide
Psychopharmacology
|January 1, 1981
Summary
Chlordiazepoxide (CDP) reduces the partial reinforcement extinction effect in rats, similar to sodium amylobarbitone. Its effects align with the conditioned-frustration hypothesis, suggesting it attenuates responses to conditioned frustrative stimuli.
Area of Science:
- Neuroscience
- Pharmacology
- Behavioral Psychology
Background:
- Anti-anxiety drugs, such as chlordiazepoxide (CDP), are known to affect learning and behavior.
- The partial reinforcement extinction effect (PREE) is a phenomenon where behaviors learned under partial reinforcement are more resistant to extinction than those learned under continuous reinforcement.
Purpose of the Study:
- To investigate the effects of chlordiazepoxide (CDP) on the partial reinforcement extinction effect (PREE) in rats.
- To determine if CDP's effects can be predicted by those of sodium amylobarbitone (SA).
- To assess if CDP's effects are consistent with the conditioned-frustration hypothesis.
Main Methods:
- Rats were trained in a straight alley for food reward under continuous or partial reinforcement schedules.
- Chlordiazepoxide (CDP) was administered to rats during acquisition, extinction, or both phases.
- Resistance to extinction was measured by the number of trials before the rats ceased responding.
Main Results:
- CDP administered during both acquisition and extinction reduced the PREE.
- CDP administered only during extinction increased resistance to extinction in both continuous and partial reinforcement groups.
- The effects of CDP were similar to those of sodium amylobarbitone (SA).
Conclusions:
- The findings support the prediction of CDP's effects based on SA's known effects.
- CDP's influence on the PREE is consistent with the conditioned-frustration hypothesis.
- CDP appears to attenuate responses to conditioned frustrative stimuli, impacting extinction resistance.