Gene editing may be a
potential treatment for anxiety and alcohol use disorder in adults who were
exposed to binge drinking in their adolescence, according to the results of an
animal study published in the journal Science Advances.
The study is issued by researchers from
the University of Illinois Chicago who have been studying the effects of early
life binge drinking on health later in life.
In prior research, the UIC team found
that binge drinking in adolescence alters brain chemistry at the enhancer
region of the Arc gene — for activity-regulated cytoskeleton-associated protein
immediate-early gene — and decreases Arc expression in the amygdala of both rodents
and humans. This epigenetic reprogramming of the Arc gene in the brain’s
emotion and memory center contributes to a predisposition to anxiety and
alcohol use disorder in adulthood.
In the new study, the researchers show
that this epigenetic reprogramming, which persists throughout life, actually
can be reversed with gene editing.
“Early binge drinking can have
long-lasting and significant effects on the brain and the results of this study
offer evidence that gene editing is a potential antidote to these effects,
offering a kind of factory reset for the brain, if you will,” said study senior
author Subhash Pandey, the Joseph A. Flaherty Endowed Professor of Psychiatry
and director of the Center for Alcohol Research in Epigenetics at UIC.
Pandey and his team used a gene-editing
tool called CRISPR-dCas9 in their experiments to manipulate the histone
acetylation and methylation processes at the Arc gene in models of adult rats.
These processes make genes more or less accessible for activation.
First, the researchers studied adult
rats with intermittent alcohol exposure in their adolescence, corresponding to
about age 10 to 18 in human years. They observed that when dCas9 was used to
promote acetylation, a process that loosens chromatin and allows transcription
factors to bind to the DNA, Arc gene expression normalized. And, indicators of
anxiety and alcohol consumption decreased.
Anxiety was measured through behavioral
testing, such as by documenting the exploratory activity of rats placed in maze
tests, and preference for alcohol was measured by monitoring the amount of
liquid consumed when the rats were presented with a choice of two bottles
consisting of options such as tap water, sugar water and varying concentrations
of alcohol (3%, 7% and 9%).
In a second model, the researchers
studied adult rats without early alcohol exposure. When inhibitory dCas9 was
used to promote methylation, which tightens chromatin and prevents
transcription factors from binding to DNA, Arc expression decreased and indicators
of anxiety and alcohol consumption increased.
“These results demonstrate that
epigenomic editing in the amygdala can ameliorate adult psychopathology after
adolescent alcohol exposure,” the authors report.
“Adolescent binge drinking is a serious public health issue, and this study not only helps us better understand what happens in developing brains when they are exposed to high concentrations of alcohol but more importantly gives us hope that one day we will have effective treatments for the complex and multifaceted diseases of anxiety and alcohol use disorder,” said Pandey, who is also a senior research career scientist at Jesse Brown VA Medical Center. “That this effect was seen bidirectionally validates the significance of the Arc enhancer gene in the amygdala in epigenetic reprogramming from adolescent binge drinking.”
Source: https://today.uic.edu/a-factory-reset-for-the-brain-cures-anxiety-drinking-behavior
Journal article: https://www.science.org/doi/10.1126/sciadv.abn2748
No comments:
Post a Comment