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Opioid involvement in the adaptive change of 5-HT1 receptors induced by chronic restraint.

L Cancela, M Volosin, V A Molina

European Journal of Pharmacology February 13, 1990 DOI: 10.1016/0014-2999(90)90025-2 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Rats
Interventions Naloxone Morphine Beta-endorphin
Duration 7-day immobilization period, 24-hour post-stress testing
Topics Serotonin
Citations 31
Key findings Chronic stress selectively increases behavioral reactivity to a 5-HT1 agonist through an opioid-dependent mechanism.

Abstract

Rats immobilized for 2 h daily for 7 days showed an increased behavioral response (forepaw treading and hind-limb abduction) to 5-methoxy-N,N-dimethyltryptamine (5-MeODMT) 24 h after the last stress session. An injection of naloxone before each stress session fully antagonized the increased behavioral reactivity to 5-MeODMT. Treatment with morphine or beta-endorphin associated with each immobilization session for 3 days produced a response to 5-MeODMT higher than that of animals subjected to immobilization only. Chronic immobilization for 7 days did not affect the shaking behavior induced by 5-hydroxytryptophan (5-HTP) 24 h after the last restraint session. These findings suggest that chronic stress may induce a selective adaptive change of the 5-HT1 site and activate an opioid mechanism that is most likely to be involved in the development of this adaptive change.

Comparable studies

Other preclinical and animal studies on serotonin, most cited first.

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