Mechanism connects early binge drinking to adult behaviors

University of Illinois Chicago researchers report that intermittent exposure to high levels of alcohol in adolescent animals leads to increased levels of microRNA-137 — a molecule that regulates gene expression in cells — in the brains of adults.

Their findings, which are published in the journal eNEURO, also show that blocking microRNA-137 in adulthood helps to reverse or reduce the lasting effects of youth drinking in animal models, such as increased alcohol use and anxiety.

“MicroRNA-137 is an important part of normal brain development, but when young brains are exposed to high amounts of alcohol intermittently, as happens with binge drinking behavior, the molecule’s regular function is altered,” said Subhash Pandey, professor of psychiatry and director of the UIC Center for Alcohol Research in Epigenetics. “By altering microRNA-137 levels, binge drinking actually rewires the brain.”

Pandey calls this alteration an epigenetic change, referring to changes in genes that are a result of environmental and social factors or exposures, not defects in the DNA’s code.

In his study, Pandey and his colleagues mimicked adolescent binge drinking in young rodents by exposing them to alcohol in cycles: two days of alcohol exposure followed by two days without alcohol exposure. They repeated the cycle eight times. After the rodents grew into adulthood, their behavior and brains were analyzed. They were more likely than non-exposed rodents to choose alcohol over water when presented with options and they were more likely to exhibit signs of anxiety.

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