Related Experiment Videos
Diazepam self-administration and resistance to extinction
1Department of Psychiatry, Pritzker School of Medicine, University of Chicago, IL 60637.
Pharmacology, Biochemistry, and Behavior
|September 1, 1987
Summary
Monkeys self-administered diazepam (a sedative-hypnotic drug), but continued responding for saline even after drug access ceased. This suggests diazepam influences behavior beyond its direct pharmacological effects, complicating assessments of its reinforcing properties.
Area of Science:
- Pharmacology
- Behavioral Neuroscience
Background:
- Understanding the reinforcing properties of drugs is crucial for addiction research.
- Diazepam, a benzodiazepine, is known for its anxiolytic and sedative effects.
- Assessing drug reinforcement often involves self-administration paradigms.
Purpose of the Study:
- To investigate the self-administration behavior of diazepam in non-human primates.
- To determine the dose-response relationship of diazepam self-administration.
- To examine the influence of prior diazepam exposure on responding during extinction.
Main Methods:
- Monkeys were trained to respond on a lever for diazepam or saline using successive approximation.
- A dose-response function for diazepam was established.
- Saline was substituted for diazepam to assess responding under extinction conditions.
- Prior cocaine self-administration was also studied.
Main Results:
- Diazepam self-administration was maintained at doses of 0.01-0.03 mg/kg/infusion.
- Responding for saline remained high during extinction, even after extended sessions.
- The level of responding during extinction correlated with previous diazepam intake.
- Cocaine self-administration followed by saline substitution led to a decline in responding.
Conclusions:
- Diazepam self-administration can lead to persistent responding for a non-drug reinforcer (saline) during extinction.
- This effect complicates the interpretation of diazepam's primary reinforcing properties.
- Prior drug exposure significantly influences subsequent drug-seeking behavior.