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Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice

BACKGROUND: Heavy 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...

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Autores principales: Vidal-Infer, Antonio, Aguilar, Maria A, Miñarro, Jose, Rodríguez-Arias, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542061/
https://www.ncbi.nlm.nih.gov/pubmed/22716128
http://dx.doi.org/10.1186/1744-9081-8-32
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author Vidal-Infer, Antonio
Aguilar, Maria A
Miñarro, Jose
Rodríguez-Arias, Marta
author_facet Vidal-Infer, Antonio
Aguilar, Maria A
Miñarro, Jose
Rodríguez-Arias, Marta
author_sort Vidal-Infer, Antonio
collection PubMed
description BACKGROUND: Heavy 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. METHODS: Adolescent 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. RESULTS: At 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. CONCLUSIONS: The 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.
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spelling pubmed-35420612013-01-11 Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice Vidal-Infer, Antonio Aguilar, Maria A Miñarro, Jose Rodríguez-Arias, Marta Behav Brain Funct Research BACKGROUND: Heavy 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. METHODS: Adolescent 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. RESULTS: At 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. CONCLUSIONS: The 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. BioMed Central 2012-06-20 /pmc/articles/PMC3542061/ /pubmed/22716128 http://dx.doi.org/10.1186/1744-9081-8-32 Text en Copyright ©2012 Vidal-Infer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Vidal-Infer, Antonio
Aguilar, Maria A
Miñarro, Jose
Rodríguez-Arias, Marta
Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice
title Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice
title_full Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice
title_fullStr Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice
title_full_unstemmed Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice
title_short Effect of intermittent exposure to ethanol and MDMA during adolescence on learning and memory in adult mice
title_sort effect of intermittent exposure to ethanol and mdma during adolescence on learning and memory in adult mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542061/
https://www.ncbi.nlm.nih.gov/pubmed/22716128
http://dx.doi.org/10.1186/1744-9081-8-32
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