Even low doses of alcohol cause changes in brain circuitry

Brain Connections Technology
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The study found that even low doses of alcohol primed the brain for addiction.

How many drinks are too many?

According to a recent rodent study, even small amounts of alcohol can cause epigenomic and transcriptomic changes in brain circuitry in a region that is essential for the development of addiction.

Pathways involved in preparing the brain for addiction, according to researchers at the University of Illinois at Chicago, are also linked to the highs that accompany drinking, such as euphoria and anxiolysis, a relaxed but awake sedated state.

Subhash Pandey

Subhash Pandey, director of the UIC Alcohol Epigenetics Research Center. Credit: Joshua Clark/University of Illinois Chicago

“This suggests that when the brain experiences the anti-anxiety effects of alcohol and mood enhancement, relaxation and buzz, it is also preparing for alcohol use disorder,” said study lead author Subhash Pandey, Joseph A. Flaherty. Professor of psychiatry and director of the Center for Alcohol Research in Epigenetics of the UIC Faculty of Medicine.

Pandey says that while the research doesn’t imply, for example, that a drink causes addiction in people, it does provide some insight into why certain people are more susceptible to alcohol use disorder.

“We’re seeing that dependent behaviors may not always be from high-volume, long-term habits, but rather the result of rapid epigenetic changes in the brain, which we show in this study can start to occur even at low doses,” Pandey said. who is also a senior career research scientist at the Jesse Brown Veterans Affairs Medical Center.

An article published in the magazine Molecular Psychiatry details Pandey’s experiments, which studied rats under control and alcohol exposure conditions.

In the experiments, the rodents were exposed to low concentrations of alcohol and the researchers watched as they navigated a maze. After that, the researchers used[{” attribute=””>RNA sequencing to examine brain tissue samples they had obtained after euthanasia and searched for patterns in gene expression.

When the samples were analyzed, the researchers discovered that a gene known as hypoxia inducible factor 3 alpha subunit, or Hif3a for short, was connected to behaviors such as how long rats remained in parts of the maze with enclosed (high anxiety) or open arms (low anxiety).

Alcohol increased Hif3a expression, even after low doses of exposure, and reduced anxiety. And, while many effects of alcohol are different among males and females, there was no difference between the two in this study.

“We saw that low doses, what we consider ‘social drinking,’ changes the gene expression in the amygdala, a brain region that regulates anxiety. In other words, it creates an epigenetic pathway for addiction,” Pandey said.

Pandey and his colleagues also set up additional experiments in which they blocked the gene in the amygdala of rats with or without alcohol exposure to validate its role in mediating anxiety. When Hif3a was blocked, anxiety was increased in control rats, mimicking withdrawal from chronic alcohol exposure. On the other hand, this also prevented the anti-anxiety effects of alcohol.

The researchers showed why, too. Hif3a’s chromatin — bundles of DNA and RNA — are loosely bundled, meaning the genes are easily accessible for transcription changes.

One thing the study does not suggest, however, is what level of alcohol exposure was safe for rodents. Instead, Pandey said, it’s important to know that low doses created priming for addiction. For people, he thinks the takeaway is simple — don’t assume social drinking or even “pandemic drinking” is without risk.

“Alcohol use disorder is complex and challenging to overcome. The information we learned from this study helps us to understand better what is happening in the brain and, one day, may be leveraged to develop better treatments and pharmaceuticals,” Pandey said.

Reference: “Unraveling the epigenomic and transcriptomic interplay during alcohol-induced anxiolysis” by Harish R. Krishnan, Huaibo Zhang, Ying Chen, John Peyton Bohnsack, Annie W. Shieh, Handojo Kusumo, Jenny Drnevich, Chunyu Liu, Dennis R. Grayson, Mark Maienschein-Cline and Subhash C. Pandey, 12 September 2022, Molecular Psychiatry.
DOI: 10.1038/s41380-022-01732-2

The study was funded by the National Institute on Alcohol Abuse and Alcoholism and the U.S. Department of Veterans Affairs.

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