Just Getting “Buzzed” Primes Brain for Alcohol Use Disorder

A new rodent study out of the University of Illinois Chicago (UIC) suggests even small quantities of alcohol can trigger epigenomic and transcriptomic changes in an area of the brain that plays a crucial role in addiction.

The study also found that the pathways involved in priming the brain for addiction are the same ones that are associated with the highs of drinking, like euphoria and anxiolysis, the clinical term for a level of sedation in which a person is relaxed but awake.  “This suggests that when the brain experiences the anti-anxiety effects of alcohol and the mood lift—the relaxation and the buzz—it is also being primed for alcohol use disorder,” said the study’s senior author Subhash Pandey, the Joseph A. Flaherty endowed professor of psychiatry and director of the Center for Alcohol Research in Epigenetics in the UIC College of Medicine. 

While Pandey says the study does not suggest one drink leads to addiction in humans, it does provide some clues as to why some people are more vulnerable to alcohol use disorder.   “We’re seeing that dependent behaviors may not always be from long-term, high-quantity habits but a result of rapid epigenetic changes in the brain, which we show in this study may start happening even at low doses,” said Pandey, who is also a senior research career scientist at the Jesse Brown Veterans Affairs Medical Center.

The study, published recently in Molecular Psychiatry, exposed rodents to low concentrations of alcohol and observed their behaviors as they explored a maze. Then the researchers analyzed brain tissue samples, collected after euthanasia, with RNA sequencing and looked for gene expression patterns.  They found that a gene called hypoxia inducible factor 3 alpha subunit (Hif3a) was associated with changes in the brain after alcohol exposure and behaviors, like how long rats stayed in areas 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 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 also showed why this happened. Hif3a’s chromatin, which are bundles of DNA and RNA, is loosely bundled, meaning the genes are easily accessible for transcription changes.

The study does not point to what level of alcohol exposure was safe for rodents. Instead, Pandey said, it’s important to consider that low doses primed the brain for addiction. For people, he thinks the takeaway is that social drinking is not 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.