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Long‐Lasting Effects of Chronic Intermittent Alcohol Exposure in Adolescent Mice on Object Recognition and Hippocampal Neuronal Activity
Author(s) -
Beaudet Gregory,
Valable Samuel,
Bourgine Joanna,
LelongBoulouard Véronique,
Lanfumey Laurence,
Freret Thomas,
Boulouard Michel,
Paizanis Eleni
Publication year - 2016
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/acer.13256
Subject(s) - hippocampus , psychology , spontaneous alternation , hippocampal formation , dentate gyrus , recognition memory , neuroscience , context (archaeology) , prefrontal cortex , perirhinal cortex , elevated plus maze , cognition , anxiety , psychiatry , biology , paleontology
Background Binge drinking is popular and highly prevalent in teenagers. However, the long‐term cognitive and neurobiological consequences of such practices are not yet fully understood. In this context, we therefore assessed in mice whether a chronic intermittent alcohol (CIA) exposure in adolescence had long‐term consequences on object discrimination and memory performances, emotional behaviors, brain activity, and morphology. Methods C57 BL /6 JR j mice were treated with either saline or ethanol (EtOH) (2 g/kg/d, i.p., from postnatal days [PND] 30 to PND 44 every other day). The day following the last administration or later in adulthood ( PND 71) mice were tested for different behavioral tests (novel object recognition, spontaneous alternation, light–dark box, elevated plus‐maze, actimeter test), to assess object recognition, working memory performances, anxiety‐like behavior, and locomotor activity. We also investigated neuronal activation of hippocampus, prefrontal and perirhinal cortices, and anatomical changes using immediate‐early gene expression and longitudinal brain magnetic resonance imaging. Results Our results showed that adolescent mice exposed to CIA present a critical and persistent impairment of short‐term object recognition performances. By contrast, spatial working memory was not impaired, nor was anxiety‐like behavior. This altered object discrimination was associated with a biphasic change in neuronal activity in the hippocampus but without morphological changes. Indeed, c‐Fos expression was specifically increased in the dorsal dentate gyrus (DG) of the hippocampus after the binge exposure, but then became significantly lower in adulthood both in the DG and the CA 1 part of the hippocampus compared with adult saline pretreated mice. Conclusions These findings provide evidence for adolescent vulnerability to the effects of intermittent binge EtOH exposure on object discrimination and hippocampal activity with long‐lasting consequences.