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How do tranquilizing agents selectively inhibit conditioned avoidance responding?
Psychopharmacology
|January 1, 1984
Summary
Tranquilizing drugs selectively inhibit conditioned avoidance responses (CAR) by impairing motor initiation, not associative learning. This effect stems from the differential response strengths between CAR and escape responses (ER).
Area of Science:
- Neuroscience
- Behavioral Pharmacology
- Animal Models
Background:
- Tranquilizing agents often inhibit conditioned avoidance responses (CAR) at doses that do not affect escape responses (ER).
- This selective action has been hypothesized to result from differences in the response strengths of CAR and ER.
Purpose of the Study:
- To investigate the hypothesis that the selective inhibition of CAR by tranquilizing agents is due to differential response strengths.
- To determine if drugs differentially affect CAR and ER based on shock intensity and response probability.
Main Methods:
- Rats were trained to perform CAR and ER in an operant chamber, with shock intensity adjusted to equalize response probability and latency.
- The effects of chlorpromazine, clonidine, diazepam, and morphine on CAR and ER were assessed at varying shock intensities.
Main Results:
- Drugs that reduced CAR by 30%-50% did not significantly affect high-shock ER (ER on CAR trials where no CAR occurred).
- These same drug doses interfered with low-shock ER to the same extent as CAR.
- A small differential effect of chlorpromazine on CAR and low-shock ER across trials suggested potentially different underlying mechanisms.
Conclusions:
- The selective blockade of CAR by tranquilizing drugs in this paradigm is primarily attributed to differential strengths between CAR and ER.
- These findings support the view that tranquilizing drugs impair avoidance behavior by hindering motor response initiation, rather than affecting associative processes or emotional reactions.
- However, subtle differential effects suggest that distinct mechanisms might underlie the suppression of CAR and low-shock ER.