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Addiction BiologyVolume 17, Issue 3, May 2012, Pages 588-600

Adolescent pre-exposure to ethanol and 3,4-methylenedioxymethylamphetamine (MDMA) increases conditioned rewarding effects of MDMA and drug-induced reinstatement(Article)

  • Ribeiro Do Couto, B.,
  • Daza-Losada, M.,
  • Rodríguez-Arias, M.,
  • Nadal, R.,
  • Guerri, C.,
  • Summavielle, T.,
  • Miñarro, J.,
  • Aguilar, M.A.
  • View Correspondence (jump link)
  • aDepartamento de Anatomía Humana y Psicobiología, Facultad de Psicología, Universidad de Murcia, Spain
  • bDepartamento de Psicobiologia, Facultad de Psicología, Universidad de Valencia, Avda. Blasco Ibáñez, 21, 46010 Valencia, Spain
  • cUnitat de Psicobiologia, Institut de Neurociencies, Universitat Autonoma de Barcelona, Spain
  • dLaboratorio de Patología Celular, Centro de Investigación Príncipe Felipe, Valencia, Spain
  • eInstituto de Biologia Molecular e Celular (IBMC), Universidade Do Porto, Portugal

Abstract

Many adolescents often take ethanol (EtOH) in combination with 3,4-methylenedioxymethylamphetamine (MDMA). In the present work, we used a mouse model to study the effect of repeated pre-exposure during adolescence to EtOH (2 g/kg), MDMA (10 or 20 mg/kg) or EtOH + MDMA on the rewarding and reinstating effects of MDMA in the conditioned place preference (CPP) paradigm. Pre-exposure to EtOH, MDMA or both increased the rewarding effects of a low dose of MDMA (1.25 mg/kg). These pre-treatments did not affect the acquisition of the CPP induced by 5 mg/kg of MDMA. However, the CPP was more persistent in mice pre-exposed to both doses of MDMA or to EtOH + MDMA20. After extinction of the CPP induced by 5 mg/kg of MDMA, reinstatement was observed in all groups with a priming dose of 2.5 mg/kg of MDMA, in the groups pre-exposed to EtOH or MDMA alone with a priming dose of 1.25 mg/kg, and in the groups pre-treated with MDMA alone with a priming dose of 0.625 mg/kg. Pre-treatment during adolescence with MDMA or EtOH induced long-term changes in the level of biogenic amines [dihydroxyphenyl acetic acid, homovanillic acid, dopamine turnover, serotonin (5-hydroxytryptamine, 5-HT) and 5-hydroxyindole acetic acid (5-HIAA) in the striatum, and 5-HT and 5-HIAA in the cortex] after the first reinstatement test, although these effects depended on the dose used during conditioning. These results suggest that exposure to EtOH and MDMA during adolescence reinforces the addictive properties of MDMA. © 2011 Society for the Study of Addiction.

Author keywords

Adolescenceconditioned place preferenceethanolMDMAmicereinstatement

Indexed keywords

EMTREE drug terms:3,4 methylenedioxymethamphetamine5 hydroxyindoleacetic acidacetic acidalcoholdopaminehomovanillic acidserotonin
EMTREE medical terms:adolescent healthalcohol consumptionanimal experimentarticlecontrolled studycorpus striatumdopamine metabolismlong term exposuremalemousenonhumanoutcome assessmentphysical chemistryplace preferencepriority journalrewardsubstance abuse
MeSH:AnimalsBiogenic AminesCentral Nervous System DepressantsCerebral CortexConditioning (Psychology)Corpus StriatumEthanolExtinction, PsychologicalMaleMiceN-Methyl-3,4-methylenedioxyamphetamineRewardSerotonin Agents

Chemicals and CAS Registry Numbers:

3,4 methylenedioxymethamphetamine, 42542-10-9; 5 hydroxyindoleacetic acid, 1321-73-9, 54-16-0; acetic acid, 127-08-2, 127-09-3, 64-19-7, 71-50-1; alcohol, 64-17-5; dopamine, 51-61-6, 62-31-7; homovanillic acid, 306-08-1; serotonin, 50-67-9;

Biogenic Amines; Central Nervous System Depressants; Ethanol, 64-17-5; N-Methyl-3,4-methylenedioxyamphetamine, 42542-10-9; Serotonin Agents

  • ISSN: 13556215
  • CODEN: ADBIF
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1111/j.1369-1600.2011.00382.x
  • PubMed ID: 21995421
  • Document Type: Article

  Aguilar, M.A.; Departamento de Psicobiologia, Facultad de Psicología, Universidad de Valencia, Avda. Blasco Ibáñez, 21, Spain;
© Copyright 2012 Elsevier B.V., All rights reserved. © MEDLINE® is the source for the MeSH terms of this document.

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