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Does increasing stress change the behavioral action of mescaline from disruption to facilitation?

David A. Gorelick, Wagner H. Bridger

Psychopharmacology January 1, 1975 DOI: 10.1007/bf00428913 via OpenAlex

Summary

AI-generated from the abstract

Rats trained to a high, stable rate of shuttlebox avoidance were given saline, saline plus a stressor, mescaline, or mescaline plus a stressor. Saline treatments had no effect on avoidance rate. Mescaline significantly decreased avoidance rate, and the decrease was greater when the stressor was also present. The stressor alone did not alter behavior. These results suggest that exposure to a stressor is not the crucial factor causing hallucinogens to have facilitatory effects on animal behavior, contrary to the hypothesis that hallucinogens facilitate behavior under stress and disrupt it otherwise.

Study at a glance

Characteristics Experiment Peer reviewed
Population Male Long-Evans rats
Interventions saline mescaline hydrochloride
Dose 36.6 mg/kg i.p. and 39.6 mg/kg i.p.
Duration Sessions began 20 min after injection; 100 trials per session; treatments at 6-day intervals
Topics Mescaline
Keywords Facilitation Psychology Saline Stressor
Citations 5
Key finding Mescaline decreased avoidance rate, and the decrease was greater when combined with a stressor, suggesting stressor exposure is not the crucial factor for facilitatory effects of hallucinogens.

Abstract

This experiment is related to the hypothesis of Bridger and of Wray that hallucinogens have facilitatory effects on animal behavior when stress is part of the experiment and have disruptive effects otherwise. Male Long-Evans rats were trained to high (above 89%), stable base line rates of shuttlebox avoidance, then given each of four treatments at 6-day intervals after returning to base line avoidance rates: 1. saline (1 ml i.p.), 2. saline+stressor, 3. mescaline hydrochloride (36.6 mg/kg i.p.), 4. mescaline (39.6 mg/kg i.p.)+stressor. Stress treatment was 1.0 mA footshock (1 sec duration) every 20-30 sec for 15 min between injection and session. Sessions (100 trials) began 20 min after injection. Treatments 1 and 2 had no effect on avoidance rate. Treatments 3 and 4 significantly decreased avoidance rate, with the latter causing significantly more decrease than the former. None of the treatments affected presession (5 min adaptation period) or intertrial crossings of the shuttlebox or latency on escape trials. These results suggest that exposure to a stressor, per se, is not the crucial factor causing hallucinogens to have facilitatory effects on animal behavior.

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