Adolescent Intermittent Ethanol Drives Modest Neuroinflammation but Does Not Escalate Drinking in Male Rats

• Published in: Cells (Basel, Switzerland) Switzerland), 2023-11, Vol.12 (21), p.2572
• Main Authors: Wooden, Jessica I, Peacoe, Lauren E, Anasooya Shaji, Chinchusha, Melbourne, Jennifer K, Chandler, Cassie M, Bardo, Michael T, Nixon, Kimberly
• Format: Article
• Language: English
• Subjects: Abstinence; adolescence; Adolescents; Alcohol; Alcohol Drinking - adverse effects; Alcohol use; Alcohol, Denatured; Alcoholism - metabolism; Animals; astrocytes; Behavior; Brain; Brain - metabolism; Cell death; Child development; Drinking behavior; Drinking of alcoholic beverages; Ethanol; Ethanol - pharmacology; Experiments; Health aspects; Housing conditions; Immune response; Inflammation; Laboratory animals; Male; Males; microglia; Neurodegeneration; Neuroinflammatory Diseases; Psychological aspects; Rats; Social aspects; social isolation; stress; Teenagers; Vimentin; Youth
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells12212572

During adolescence, the brain is highly susceptible to alcohol-induced damage and subsequent neuroimmune responses, effects which may enhance development of an alcohol use disorder (AUD). Neuroimmune reactions are implicated in adolescent alcohol exposure escalating adulthood drinking. Therefore, we investigated whether intermittent alcohol exposure in male, adolescent rats (AIE) escalated adult drinking via two-bottle choice (2BC). We also examined the influence of housing environment across three groups: standard (group-housed with enrichment during 2BC), impoverished (group-housed without enrichment during 2BC), or isolation (single-housed without bedding or enrichment throughout). In the standard group immediately after AIE/saline and after 2BC, we also examined the expression of microglial marker, Iba1, reactive astrocyte marker, vimentin, and neuronal cell death dye, FluoroJade B (FJB). We did not observe an escalation of adulthood drinking following AIE, regardless of housing condition. Further, only a modest neuroimmune response occurred after AIE in the standard group: no significant microglial reactivity or neuronal cell death was apparent using this model, although some astrocyte reactivity was detected in adolescence following AIE that resolved by adulthood. These data suggest that the lack of neuroimmune response in adolescence in this model may underlie the lack of escalation of alcohol drinking, which could not be modified through isolation stress.