Adolescent Ethanol Exposure Alters Cholinergic Function and Apical Dendritic Branching Within the Orbital Frontal Cortex

• Published in: Neuroscience Vol. 473; pp. 52 - 65
• Main Authors: Kipp, B.T., Nunes, P.T., Galaj, E., Hitchcock, B., Nasra, T., Poynor, K.R., Heide, S.K., Reitz, N.L., Savage, L.M.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01-10-2021
• Subjects: acetylcholine; adolescence; Brain; Cholinergic Agents; ethanol; Ethanol - toxicity; Frontal Lobe; orbital frontal cortex; Prefrontal Cortex; CON; MS/DB; orbital frontal cortex; ACh; HDB; PFC; OFC; ethanol; SI; ChAT; NbM; adolescence; acetylcholine; AIE; VAChT
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/j.neuroscience.2021.08.014

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•Adolescent ethanol decreases cholinergic markers in the basal forebrain and cortex.•Adolescent ethanol suppresses of behaviorally-activated acetylcholine efflux.•Cholinergic dysfunction influences impairments seen with adolescence alcohol abuse.
During adolescence, heavy binge-like ethanol consumption can lead to frontocortical structural and functional impairments. These impairments are likely driven by adolescence being a critical time point for maturation of brain regions associated with higher-order cognitive functioning. Rodent models of heavy binge-like ethanol exposure show consistent disruptions to the typical development of the prefrontal cortex (PFC). All deep cortical layers receive cholinergic projections that originate from the Nucleus basalis of Meynert (NbM) complex. These cholinergic projections are highly involved in learning, memory, and attention. Adolescent intermittent ethanol exposure (AIE) induces cholinergic dysfunction as a result of an epigenetic suppression of the genes that drive the cholinergic phenotype. The current study used a model of AIE to assess structural and functional changes to the frontal cortex and NbM following binge-like ethanol exposure in adolescence. Western blot analysis revealed long-term disruptions of the cholinergic circuit following AIE: choline acetyltransferase (ChAT) was suppressed in the NbM and vesicular acetylcholine transporter (VAChT) was suppressed in the orbitofrontal cortex (OFC). In vivo microdialysis for acetylcholine efflux during a spatial memory task determined changes in cholinergic modulation within the PFC following AIE. However, AIE spared performance on the spatial memory task and on an operant reversal task. In a second study, Golgi-Cox staining determined that AIE increased apical dendritic complexity in the OFC, with sex influencing whether the increase in branching occurred near or away from the soma. Spine density or maturity was not affected, likely compensating for a disruption in neurotransmitter function following AIE.