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18-Methoxycoronaridine blocks acquisition but enhances reinstatement of a cocaine place preference.

Sarah E McCallum, Stanley D Glick

Neuroscience Letters April 11, 2009 DOI: 10.1016/j.neulet.2009.04.019 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational study Peer reviewed
Population Male Sprague-Dawley rats
Interventions 18-methoxycoronaridine (18-MC) Cocaine
Topics Ibogaine
Keywords Animals Rats, sprague-dawley Cocaine Dopamine uptake inhibitors Self administration Analysis of variance Behavior, animal Behavior, addictive Conditioning, operant Time factors Male Extinction, psychological Reinforcement, psychology
Key findings 18-MC attenuated acquisition of a cocaine conditioned place preference but did not affect its expression and enhanced reinstatement after extinction. The authors argue that acquisition, expression, and reinstatement of a CPP likely involve separate mechanisms.

Abstract

The iboga alkaloid congener, 18-methoxycoronaridine (18-MC), decreases self-administration of multiple drugs of abuse. Here, in a biased procedure, we investigated whether 18-MC would have a similar effect on the acquisition, expression and reinstatement of a cocaine conditioned place preference (CPP) in male Sprague-Dawley rats. While 18-MC attenuated acquisition of a cocaine CPP, it had no effect on CPP expression, and enhanced the reinstatement of cocaine CPP following extinction. Our results are consistent with those obtained using ibogaine, but reinforce the notion that acquisition, expression and reinstatement of a CPP likely involve separate mechanisms.

Comparable studies

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

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