Abstract
A growing body of evidence indicates that the intake of large amounts of alcohol during one session may have structural and functional effects on the still-maturing brains of young people. These effects are particularly pronounced in prefrontal and hippocampal regions, which appear to be especially sensitive to the neurotoxic effects of alcohol. However, to date, few studies have used the event-related potentials (ERPs) technique to analyze the relationship between binge drinking (BD) and associative memory. The objective of this study was to examine brain activity during memory encoding using the Subsequent memory paradigm in subjects who have followed a BD pattern of alcohol consumption for at least 2 years. A total of 50 undergraduate students (mean age = 20.6 years), i.e., 25 controls (12 females) and 25 binge drinkers (BDs; 11 females), with no personal or family history of alcoholism or psychopathological disorders, performed a visual face–name association memory task. The task used enables assessment of the Difference due to memory effect (Dm), a measure of memory encoding based on comparison of the neural activity associated with subsequent successful and unsuccessful retrieval. In ERP studies, study items that are subsequently remembered elicit larger positive amplitudes at midline parieto-frontal sites than those items that are subsequently forgotten. The Dm effect generally appears in the latency range of about 300–800 ms. The results showed a Dm effect in posterior regions in the 350–650 ms latency range in the Control group. However, in the BD group, no significant differences were observed in the electrophysiological brain activity between remembered and forgotten items during the encoding process. No differences between groups were found in behavioral performance. These findings show that young BDs display abnormal pattern of ERP brain activity during the encoding phase of a visual face–name association task, possibly suggesting a different neural signature of successful memory encoding.
Highlights
Binge drinking (BD) is a pattern of alcohol consumption characterized by the intake of five or more drinks on a single occasion within a 2-h interval, reaching blood alcohol concentration to 0.08 g/dL [1] at least once in the last month [2].The most recent report of the World Health Organization [3] has highlighted that the highest rates of binge drinkers (BDs) among young people occur in Europe (31.2%), the USA (18.4%) and the Western Pacific Region (12.5%)
In accordance with animal studies, this period is sensitive to the effects of BD, which causes more brain damage in adolescent than in adult rats, especially in the prefrontal cortex and the hippocampus [6, 7]
event-related potentials (ERPs) were used to examine the effects of alcohol BD on declarative memory encoding among undergraduate students, using a subsequent memory paradigm with a visual face–name association memory task
Summary
Binge drinking (BD) is a pattern of alcohol consumption characterized by the intake of five or more drinks (four or more for females) on a single occasion within a 2-h interval, reaching blood alcohol concentration to 0.08 g/dL [1] at least once in the last month [2].The most recent report of the World Health Organization [3] has highlighted that the highest rates of BD among young people occur in Europe (31.2%), the USA (18.4%) and the Western Pacific Region (12.5%). The rate reaches 41.8% in the 18–25 age range [4]. Memory Encoding in BD concern for public authorities because of its adverse impact on a wide range of personal, social, and health issues and because of the associated economic cost. Adolescence is a critical stage of development in which the brain undergoes processes of neuromaturation and reorganization [5], which extend into the third decade of life. In accordance with animal studies, this period is sensitive to the effects of BD, which causes more brain damage in adolescent than in adult rats, especially in the prefrontal cortex and the hippocampus [6, 7]. It has been shown that these alterations can lead to long-lasting changes in the adult brain [8, 9]
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