Long-Term Effects of Intermittent Adolescent Alcohol Exposure in Male and Female Rats.

dc.contributor.authorMarco, Eva M
dc.contributor.authorPeñasco, Sara
dc.contributor.authorHernández, María-Donina
dc.contributor.authorGil, Anabel
dc.contributor.authorBorcel, Erika
dc.contributor.authorMoya, Marta
dc.contributor.authorGiné, Elena
dc.contributor.authorLópez-Moreno, José Antonio
dc.contributor.authorGuerri, Consuelo
dc.contributor.authorLópez-Gallardo, Meritxell
dc.contributor.authorRodríguez de Fonseca, Fernando
dc.date.accessioned2025-01-07T16:16:57Z
dc.date.available2025-01-07T16:16:57Z
dc.date.issued2017-11-28
dc.description.abstractAlcohol is a serious public health concern that has a differential impact on individuals depending upon age and sex. Patterns of alcohol consumption have recently changed: heavy episodic drinking-known as binge-drinking-has become most popular among the youth. Herein, we aimed to investigate the consequences of intermittent adolescent alcohol consumption in male and female animals. Thus, Wistar rats were given free access to ethanol (20% in drinking water) or tap water for 2-h sessions during 3 days, and for an additional 4-h session on the 4th day; every week during adolescence, from postnatal day (pnd) 28-52. During this period, animals consumed a moderate amount of alcohol despite blood ethanol concentration (BEC) did not achieve binge-drinking levels. No withdrawal signs were observed: no changes were observed regarding anxiety-like responses in the elevated plus-maze or plasma corticosterone levels (pnd 53-54). In the novel object recognition (NOR) test (pnd 63), a significant deficit in recognition memory was observed in both male and female rats. Western Blot analyses resulted in an increase in the expression of synaptophysin in the frontal cortex (FC) of male and female animals, together with a decrease in the expression of the CB2R in the same brain region. In addition, adolescent alcohol induced, exclusively among females, a decrease in several markers of dopaminergic and serotonergic neurotransmission, in which epigenetic mechanisms, i.e., histone acetylation, might be involved. Taken together, further research is still needed to specifically correlate sex-specific brain and behavioral consequences of adolescent alcohol exposure.
dc.identifier.doi10.3389/fnbeh.2017.00233
dc.identifier.issn1662-5153
dc.identifier.pmcPMC5712378
dc.identifier.pmid29234279
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC5712378/pdf
dc.identifier.unpaywallURLhttps://www.frontiersin.org/articles/10.3389/fnbeh.2017.00233/pdf
dc.identifier.urihttps://hdl.handle.net/10668/27728
dc.journal.titleFrontiers in behavioral neuroscience
dc.journal.titleabbreviationFront Behav Neurosci
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Málaga - Plataforma Bionand (IBIMA)
dc.organizationSAS - Hospital Universitario Regional de Málaga
dc.page.number233
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectadolescence
dc.subjectalcohol
dc.subjectcognitive function
dc.subjectdrinking-in-the-dark
dc.subjectfrontal cortex
dc.subjecthippocampal formation
dc.subjectneural plasticity
dc.subjectsex differences
dc.titleLong-Term Effects of Intermittent Adolescent Alcohol Exposure in Male and Female Rats.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11

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