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Effects of repeated alcohol abstinence on within-subject prefrontal cortical gene expression in rhesus macaques. | LitMetric

AI Article Synopsis

  • A study involving 24 male rhesus monkeys examined the effects of chronic ethanol self-administration and compared gene expression in the prefrontal cortex before and after this process.
  • After 14 months of alcohol exposure, biopsies and necropsies revealed significant changes in gene expression, particularly in genes related to immune response and regulating MAP kinase activity, which were affected by the level of alcohol consumption.
  • The findings highlight the potential of using non-human primate models to understand genomic changes related to alcohol use and may provide new targets for treating severe drinking behaviors following abstinence.

Article Abstract

Male rhesus monkeys ( = 24) had a biopsy of prefrontal cortical area 46 prior to chronic ethanol self-administration ( = 17) or caloric control ( = 7). Fourteen months of daily self-administration (water vs. 4% alcohol, 22 h access/day termed "open-access") was followed by two cycles of prolonged abstinence (5 weeks) each followed by 3 months of open-access alcohol and a final abstinence followed by necropsy. At necropsy, a biopsy of Area 46, contralateral to the original biopsy, was obtained. Gene expression data (RNA-Seq) were collected comparing biopsy/necropsy samples. Monkeys were categorized by drinking status during the final post-abstinent drinking phase as light (LD), binge (BD), heavy (HD) and very heavy (VHD drinkers). Comparing pre-ethanol to post-abstinent biopsies, four animals that converted from HD to VHD status had significant ontology enrichments in downregulated genes (necropsy minus biopsy = 286) that included immune response (FDR < 9 × 10) and plasma membrane changes (FDR < 1 × 10). Genes in the immune response category included and , , , , and , and . Upregulated genes ( = 388) were particularly enriched in genes associated with the negative regulation of MAP kinase activity (FDR < 3 × 10), including , , , and , , , and , , and . Overall, these data illustrate the power of the NHP model and the within-subject design of genomic changes due to alcohol and suggest new targets for treating severe escalated drinking following repeated alcohol abstinence attempts.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11082748PMC
http://dx.doi.org/10.3389/adar.2024.12528DOI Listing

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