Skip to content
View Categories

Emerging role of epigenetic mechanisms in alcohol addiction

< 1 min read

Alcohol use disorder (AUD) is a complex brain disorder with a number of persistent behavioral and neurochemical manifestations. Both genetic and environmental factors are known to contribute to the development of AUD, and recent studies of alcohol exposure and subsequent changes in gene expression suggest the importance of epigenetic mechanisms.

In particular, histone modifications and DNA methylation have emerged as important regulators of gene expression and associated phenotypes of AUD.

Given the therapeutic potential of epigenetic targets, this review aims to summarize the role of epigenetic regulation in our current understanding of AUD by evaluating known epigenetic signatures of brain regions critical for addictive behavior in animal and human studies at different stages of AUD. More specifically, the effects of acute and chronic alcohol exposure, tolerance, and post-exposure withdrawal on epigenetically induced changes in gene expression and synaptic plasticity in key brain regions and associated behavioral phenotypes were discussed.

Understanding the contribution of epigenetic regulation to crucial signaling pathways may prove critical for the future development of novel biomarkers and treatment agents to alleviate or prevent AUD.


Alcohol Clin Exp Res.: Emerging role of epigenetic mechanisms in alcohol addiction

Found at Alkohol adé (german)

Powered by BetterDocs

Close Popup

Even Bye Bye Booze needs a few cookies,.

However, we try only to activate as few as possible technically necessary cookies so that your visit to this site cannot be tracked as far as possible by third parties. We do not share any information about your visit with anyone.

But even we we do need a few - e.g. to display this legal notice or to care for that you do not have to log in again for each page or see this popup again for each page.

As soon as you click on an external link or video, cookies may be set by the operators of these sites, which we cannot influence. Learn more on our privacy page.


Close Popup