Abstract

BackgroundHeavy binge drinking is increasingly frequent among adolescents, and consumption of 3,4-methylenedioxymethamphetamine (MDMA) is often combined with ethanol (EtOH). The long-lasting effects of intermittent exposure to EtOH and MDMA during adolescence on learning and memory were evaluated in adult mice using the Hebb-Williams maze.MethodsAdolescent OF1 mice were exposed to EtOH (1.25 g/kg) on two consecutive days at 48-h intervals over a 14-day period (from PD 29 to 42). MDMA (10 or 20 mg/kg) was injected twice daily at 4-h intervals over two consecutive days, and this schedule was repeated six days later (PD 33, 34, 41 and 42), resulting in a total of eight injections. Animals were initiated in the Hebb-Williams maze on PND 64. The concentration of brain monoamines in the striatum and hippocampus was then measured.ResultsAt the doses employed, both EtOH and MDMA, administered alone or together, impaired learning in the Hebb-Williams maze, as treated animals required more time to reach the goal than their saline-treated counterparts. The groups treated during adolescence with EtOH, alone or plus MDMA, also presented longer latency scores and needed more trials to reach the acquisition criterion score. MDMA induced a decrease in striatal DA concentration, an effect that was augmented by the co-administration of EtOH. All the treatment groups displayed an imbalance in the interaction DA/serotonin.ConclusionsThe present findings indicate that the developing brain is highly vulnerable to the damaging effects of EtOH and/or MDMA, since mice receiving these drugs in a binge pattern during adolescence exhibit impaired learning and memory in adulthood.

Highlights

  • Heavy binge drinking is increasingly frequent among adolescents, and consumption of 3,4methylenedioxymethamphetamine (MDMA) is often combined with ethanol (EtOH)

  • Monoamine levels were significantly affected by treatment during adolescence, with a significant decrease of striatal DA being observed in the groups treated with 20 mg/kg of MDMA, alone or plus EtOH and in the groups treated with 10 mg/kg of MDMA plus EtOH, confirming that EtOH increases the neurotoxic effect of MDMA in mice

  • We have previously described the deleterious effect of intermittent intensive EtOH ingestion during adolescence on learning and memory in rats [30]

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Summary

Introduction

Heavy binge drinking is increasingly frequent among adolescents, and consumption of 3,4methylenedioxymethamphetamine (MDMA) is often combined with ethanol (EtOH). MDMA (3,4-methylenedioxymethamphetamine) users consume ethanol frequently (EtOH) [1,2]. In a survey of Spanish adolescents, 49.6% of those who had consumed alcohol in the previous month reported getting drunk during binges. Among those who consumed ecstasy, 98% admitted taking. EtOH is an allosteric modulator of many transmembrane receptors [9]. It acts primarily as a CNS depressant, potentiating the action of GABA at the GABAA receptor [10]. MDMA, on the other hand, causes a rapid efflux of dopamine (DA) and serotonin (5-HT) in several brain areas immediately after it is administered, including the striatum and nucleus accumbens (NAc), [11]

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