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McClung J, Fantegrossi W, Howell LL: Reinstatement of extinguished amphetamine self-administration by 3,4-methylenedioxymethamphetamine (MDMA) and its enantiomers in rhesus monkeys. Psychopharmacology. 2010 Mar 23. RATIONALE: The effectiveness of MDMA and its enantiomers to reinstate responding previously maintained by drug self-administration has not been thoroughly investigated. OBJECTIVES: The present study was designed to compare the reinstatement effects of amphetamine, the piperazine-analog BZP, SR (+/-)-MDMA, S (+)-MDMA, R (-)-MDMA, and fenfluramine on behavior maintained under a second-order schedule of intravenous amphetamine self-administration in rhesus monkeys (n=4). METHODS: Following saline substitution and extinction, a range of doses of amphetamine, BZP, SR (+/-)-MDMA, S (+)-MDMA, R (-)-MDMA, and fenfluramine were administered i.v. as non-contingent priming injections in order to characterize their effectiveness to reinstate responding previously maintained by amphetamine self-administration. RESULTS: Priming injections of amphetamine, BZP, SR (+/-)-MDMA, and S (+)-MDMA induced significant reinstatement effects. In contrast, neither R (-)-MDMA nor fenfluramine effectively reinstated behavior. Pretreatment with the selective serotonin transporter inhibitor, fluoxetine, attenuated the reinstatement effects of SR (+/-)-MDMA, S (+)-MDMA, and BZP but had no significant effect on amphetamine-primed reinstatement. CONCLUSIONS: Given the profile of neurochemical effects published previously, these findings suggest that the reinstatement effects of MDMA are mediated primarily by dopamine release; however, the attenuation of MDMA-induced reinstatement by fluoxetine supports previous research demonstrating the complex behavioral pharmacology of MDMA-like drugs and that the reinstatement effects of MDMA are at least partially mediated by serotonergic mechanisms. |
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