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

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 pr...

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Veröffentlicht in:Advances in Drug and Alcohol Research 2024, Vol.4, p.12528
Hauptverfasser: Hitzemann, Robert, Gao, Lina, Fei, Suzanne S, Ray, Karina, Vigh-Conrad, Katinka A, Phillips, Tamara J, Searles, Robert, Cervera-Juanes, Rita P, Khadka, Rupak, Carlson, Timothy L, Gonzales, Steven W, Newman, Natali, Grant, Kathleen A
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Sprache:eng
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Zusammenfassung: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.
ISSN:2674-0001
2674-0001
DOI:10.3389/adar.2024.12528