AI Article Synopsis

  • Adolescent binge drinking increases the risk of alcohol use disorders in adulthood, making it crucial to study its effects on brain health and cognitive function.
  • Research on rats exposed to intermittent ethanol revealed significant impairments in nonspatial working memory and behavioral flexibility, with both male and female rats showing deficits in memory and adaptability.
  • The study found a decrease in cholinergic interneurons in a brain region called the nucleus accumbens, suggesting long-term cognitive and behavioral issues linked to adolescent binge drinking.

Article Abstract

Adolescent binge drinking renders young drinkers vulnerable to alcohol use disorders in adulthood; therefore, understanding alcohol-induced brain damage and associated cognitive dysfunctions is of paramount importance. Here we investigated the effects of binge-like adolescent intermittent ethanol (AIE) exposure on nonspatial working memory, behavioral flexibility and cholinergic alterations in the nucleus accumbens (NAc) in male and female rats. On postnatal days P25-57 rats were intubated with water or ethanol (at a dose of 5 g/kg) on a 2-day-on/2-day-off cycle and were then tested in adulthood on social recognition and probabilistic reversal learning tasks. During the social recognition task AIE-treated rats spent similar amounts of time interacting with familiar and novel juveniles, indicating an impaired ability to sustain memory of the familiar juvenile. During probabilistic reversal learning, AIE-treated male and female rats showed behavioral inflexibility as indicated by a higher number of trials needed to complete three reversals within a session, longer response latencies for lever selection, and for males, a higher number of errors as compared to water-treated rats. AIE exposure also reduced the number of cholinergic interneurons in the NAc in males and females. These findings indicate AIE-related pathologies of accumbal cholinergic interneurons and long lasting cognitive-behavioral deficits, which may be associated with cortico-striatal hypofunction.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450752PMC
http://dx.doi.org/10.1016/j.neuroscience.2019.01.062DOI Listing

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