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 |
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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. |
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ISSN: | 2674-0001 2674-0001 |
DOI: | 10.3389/adar.2024.12528 |