Abstract

A prior history of excessive drinking induces a negative affective state in both humans and laboratory rodents, the manifestation of which varies with the age of drinking-onset. In adolescent male mice, negative affect incubates over the course of a 30-day alcohol withdrawal period. In contrast, the negative affect exhibited by adult male mice is robust at 1 day withdrawal, but dissipates with the passage of time. As females tend to consume more alcohol than males, we aimed to explore the affective disturbances exhibited by adolescent and adult C57BL/6J mice of both sexes during more protracted alcohol withdrawal and to relate any behavioral changes observed to plasma corticosterone levels as a biochemical index of stress. Male and female, adolescent and adult, mice were subjected to 14 consecutive days of binge alcohol-drinking using a multi-bottle-choice Drinking-in-the-Dark (DID) procedure (5, 10, 20 and 40% v/v). Age- and sex-matched control mice consumed water only. On either withdrawal day 1 or 70, subgroups of animals were subjected a to 1-day behavioral test battery that included the light–dark box shuttle test, marble-burying test, and Porsolt forced swim test. As expected, adolescent mice consumed more alcohol than adults and females consumed more alcohol than males. However, despite binge-like levels of alcohol consumption, we detected relatively few signs of alcohol withdrawal-induced negative affect and there was no correlation between affective behavior and circulating corticosterone levels. We discuss these findings within the context of our published work, highlighting procedural differences that might account for the relatively weak effect of binge-drinking history upon anxiety and depressive-like behavior observed herein.

Highlights

  • Binge-drinking is the most common form of alcohol abuse amongst adolescents

  • In so far as we have investigated in male mice, the age-related differences in the temporal manifestation of withdrawal-induced negative affect reflect an interaction between the age of binge-drinking onset and time-dependent changes in the expression and function of glutamate receptor-related proteins within extended amygdala structures [10,24,25,26]

  • × Drinking observed for the total total time time spent spent immobile in the Depiction of the results for the adolescent-onset immobile in the Porsolt Forced Swim Test. (A) Depiction of the results for the adolescent-onset mice mice at 1-day withdrawal

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Summary

Introduction

Binge-drinking is the most common form of alcohol abuse amongst adolescents. The NationalInstitute of Alcohol Abuse and Alcoholism (NIAAA) cites that 90% of all underage drinkers within the United States have engaged in binge-drinking behaviors [1], with an estimated 1 million adolescents engaging in frequent binge-drinking episodes [2]. Brain Sci. 2020, 10, 405 is a critical period of brain development that occurs in between the ages of 12–17 in humans and approximately postnatal days (PND) 28–50 in laboratory rodents. During this period, the brain undergoes robust structural and functional changes, including alterations in neuronal connectivity and synaptic plasticity [3]. Coupled with environmental and social influences, these adolescent-related behavioral phenotypes have been theorized to increase drug abuse propensity, including excessive alcohol-drinking [8]. This increased propensity to consume alcohol is augmented by the fact that adolescents tend to be significantly less sensitive to alcohol’s negative reinforcing properties than adults, including “hang-over” and increased negative affect during early alcohol withdrawal [6,9,10]

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