Sex differences in GABA A receptor subunit transcript expression are mediated by genotype in subjects with alcohol-related cirrhosis of the liver.
Madeline K AshtonAndré Veloso RuedaAda Man-Choi HoNoradibah Arina Binte M Noor AizinHansa SharmaPeter R DoddAlfreda StadlinRosana CamariniPublished in: Genes, brain, and behavior (2022)
Male and female human subjects show contrasting propensities to misuse drugs of addiction, including alcohol. These differences lead to different psychological and neurological consequences, such as the likelihood of developing dependence. The pattern and extent of brain damage in alcohol-use disorder cases also varies with comorbid disease. To explore mechanisms that might underlie these outcomes, we used autopsy tissue to determine mRNA transcript expression in relation to genotype for two GABA A receptor subunit genes. We used quantitative Real-Time PCR to measure GABRA6 and GABRA2 mRNA concentrations in dorsolateral prefrontal and primary motor cortices of alcohol-use disorder subjects and controls of both sexes with and without liver disease who had been genotyped for these GABA A receptor subunit genes. Cirrhotic alcohol-use disorder cases had significantly higher expression of GABRA6 and GABRA2 transcripts than either controls or non-cirrhotic alcohol-use disorder cases. Differences were observed between sexes, genotypes and brain regions. We show that sex differences in subjects with GABRA6 and GABRA2 variants may contribute to differences in susceptibility to alcohol-use disorder and alcohol-induced cirrhosis.
Keyphrases
- alcohol use disorder
- binding protein
- poor prognosis
- working memory
- endothelial cells
- resting state
- white matter
- alcohol consumption
- genome wide
- real time pcr
- functional connectivity
- rna seq
- oxidative stress
- cerebral ischemia
- chronic pain
- long non coding rna
- drug induced
- gene expression
- high glucose
- metabolic syndrome
- depressive symptoms
- genome wide identification
- physical activity
- insulin resistance
- dna methylation
- adipose tissue
- transcription factor
- single cell
- weight loss