Adaptor protein complex 2 in the orbitofrontal cortex predicts alcohol use disorder

• Published in: Molecular psychiatry Vol. 28; no. 11; pp. 4766 - 4776
• Main Authors: Mulholland, Patrick J., Berto, Stefano, Wilmarth, Phillip A., McMahan, Christopher, Ball, Lauren E., Woodward, John J.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.11.2023; Nature Publishing Group
• Subjects: 38/39; 631/337; 631/378; 64/60; 82/58; Adaptor Protein Complex 2 - metabolism; Alcohol Drinking - genetics; Alcohol use; Alcoholism - metabolism; Alleles; Animals; Behavioral Sciences; Bioinformatics; Biological Psychology; Cognitive ability; Decision making; Drinking behavior; Ethanol - metabolism; Extracellular matrix; Female; Humans; Inbreeding; Learning algorithms; Machine learning; Male; Medicine; Medicine & Public Health; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Neurosciences; Pharmacotherapy; Prefrontal Cortex - metabolism; Proteins; Proteome - metabolism; Proteomes; Proteomics; Psychiatry; Social behavior; Social discrimination learning; Social interactions
• ISSN: 1359-4184; 1476-5578; 1476-5578
• DOI: 10.1038/s41380-023-02236-3

Alcohol use disorder (AUD) is a life-threatening disease characterized by compulsive drinking, cognitive deficits, and social impairment that continue despite negative consequences. The inability of individuals with AUD to regulate drinking may involve functional deficits in cortical areas that normally balance actions that have aspects of both reward and risk. Among these, the orbitofrontal cortex (OFC) is critically involved in goal-directed behavior and is thought to maintain a representation of reward value that guides decision making. In the present study, we analyzed post-mortem OFC brain samples collected from age- and sex-matched control subjects and those with AUD using proteomics, bioinformatics, machine learning, and reverse genetics approaches. Of the 4,500+ total unique proteins identified in the proteomics screen, there were 47 proteins that differed significantly by sex that were enriched in processes regulating extracellular matrix and axonal structure. Gene ontology enrichment analysis revealed that proteins differentially expressed in AUD cases were involved in synaptic and mitochondrial function, as well as transmembrane transporter activity. Alcohol-sensitive OFC proteins also mapped to abnormal social behaviors and social interactions. Machine learning analysis of the post-mortem OFC proteome revealed dysregulation of presynaptic (e.g., AP2A1) and mitochondrial proteins that predicted the occurrence and severity of AUD. Using a reverse genetics approach to validate a target protein, we found that prefrontal Ap2a1 expression significantly correlated with voluntary alcohol drinking in male and female genetically diverse mouse strains. Moreover, recombinant inbred strains that inherited the C57BL/6J allele at the Ap2a1 interval consumed higher amounts of alcohol than those that inherited the DBA/2J allele. Together, these findings highlight the impact of excessive alcohol consumption on the human OFC proteome and identify important cross-species cortical mechanisms and proteins that control drinking in individuals with AUD.