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Alcohol Metabolism and Epigenetics Changes

Metabolites, including those generated during ethanol metabolism, can impact disease states by binding to transcription factors and/or modifying chromatin structure, thereby altering gene expression patterns. For example, the activities of enzymes involved in epigenetic modifications such as DNA and...

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Autor principal: Zakhari, Samir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute on Alcohol Abuse and Alcoholism 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860421/
https://www.ncbi.nlm.nih.gov/pubmed/24313160
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author Zakhari, Samir
author_facet Zakhari, Samir
author_sort Zakhari, Samir
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description Metabolites, including those generated during ethanol metabolism, can impact disease states by binding to transcription factors and/or modifying chromatin structure, thereby altering gene expression patterns. For example, the activities of enzymes involved in epigenetic modifications such as DNA and histone methylation and histone acetylation, are influenced by the levels of metabolites such as nicotinamide adenine dinucleotide (NAD), adenosine triphosphate (ATP), and S-adenosylmethionine (SAM). Chronic alcohol consumption leads to significant reductions in SAM levels, thereby contributing to DNA hypomethylation. Similarly, ethanol metabolism alters the ratio of NAD(+) to reduced NAD (NADH) and promotes the formation of reactive oxygen species and acetate, all of which impact epigenetic regulatory mechanisms. In addition to altered carbohydrate metabolism, induction of cell death, and changes in mitochondrial permeability transition, these metabolism-related changes can lead to modulation of epigenetic regulation of gene expression. Understanding the nature of these epigenetic changes will help researchers design novel medications to treat or at least ameliorate alcohol-induced organ damage.
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spelling pubmed-38604212014-01-13 Alcohol Metabolism and Epigenetics Changes Zakhari, Samir Alcohol Res Articles Metabolites, including those generated during ethanol metabolism, can impact disease states by binding to transcription factors and/or modifying chromatin structure, thereby altering gene expression patterns. For example, the activities of enzymes involved in epigenetic modifications such as DNA and histone methylation and histone acetylation, are influenced by the levels of metabolites such as nicotinamide adenine dinucleotide (NAD), adenosine triphosphate (ATP), and S-adenosylmethionine (SAM). Chronic alcohol consumption leads to significant reductions in SAM levels, thereby contributing to DNA hypomethylation. Similarly, ethanol metabolism alters the ratio of NAD(+) to reduced NAD (NADH) and promotes the formation of reactive oxygen species and acetate, all of which impact epigenetic regulatory mechanisms. In addition to altered carbohydrate metabolism, induction of cell death, and changes in mitochondrial permeability transition, these metabolism-related changes can lead to modulation of epigenetic regulation of gene expression. Understanding the nature of these epigenetic changes will help researchers design novel medications to treat or at least ameliorate alcohol-induced organ damage. National Institute on Alcohol Abuse and Alcoholism 2013 /pmc/articles/PMC3860421/ /pubmed/24313160 Text en http://creativecommons.org/publicdomain/mark/1.0/ Unless otherwise noted in the text, all material appearing in this journal is in the public domain and may be reproduced without permission. Citation of the source is appreciated.
spellingShingle Articles
Zakhari, Samir
Alcohol Metabolism and Epigenetics Changes
title Alcohol Metabolism and Epigenetics Changes
title_full Alcohol Metabolism and Epigenetics Changes
title_fullStr Alcohol Metabolism and Epigenetics Changes
title_full_unstemmed Alcohol Metabolism and Epigenetics Changes
title_short Alcohol Metabolism and Epigenetics Changes
title_sort alcohol metabolism and epigenetics changes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860421/
https://www.ncbi.nlm.nih.gov/pubmed/24313160
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