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Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver

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 disord...

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Autores principales: Ashton, Madeline K., Rueda, André V. L., Ho, Ada M.‐C., Noor Aizin, Noradibah Arina Binte M., Sharma, Hansa, Dodd, Peter R., Stadlin, Alfreda, Camarini, Rosana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744570/
https://www.ncbi.nlm.nih.gov/pubmed/35301805
http://dx.doi.org/10.1111/gbb.12785
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author Ashton, Madeline K.
Rueda, André V. L.
Ho, Ada M.‐C.
Noor Aizin, Noradibah Arina Binte M.
Sharma, Hansa
Dodd, Peter R.
Stadlin, Alfreda
Camarini, Rosana
author_facet Ashton, Madeline K.
Rueda, André V. L.
Ho, Ada M.‐C.
Noor Aizin, Noradibah Arina Binte M.
Sharma, Hansa
Dodd, Peter R.
Stadlin, Alfreda
Camarini, Rosana
author_sort Ashton, Madeline K.
collection PubMed
description 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.
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spelling pubmed-97445702023-02-08 Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver Ashton, Madeline K. Rueda, André V. L. Ho, Ada M.‐C. Noor Aizin, Noradibah Arina Binte M. Sharma, Hansa Dodd, Peter R. Stadlin, Alfreda Camarini, Rosana Genes Brain Behav Original Articles 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. Blackwell Publishing Ltd 2022-03-18 /pmc/articles/PMC9744570/ /pubmed/35301805 http://dx.doi.org/10.1111/gbb.12785 Text en © 2022 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Ashton, Madeline K.
Rueda, André V. L.
Ho, Ada M.‐C.
Noor Aizin, Noradibah Arina Binte M.
Sharma, Hansa
Dodd, Peter R.
Stadlin, Alfreda
Camarini, Rosana
Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver
title Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver
title_full Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver
title_fullStr Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver
title_full_unstemmed Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver
title_short Sex differences in GABA(A) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver
title_sort sex differences in gaba(a) receptor subunit transcript expression are mediated by genotype in subjects with alcohol‐related cirrhosis of the liver
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744570/
https://www.ncbi.nlm.nih.gov/pubmed/35301805
http://dx.doi.org/10.1111/gbb.12785
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