Little is known about liver disruption that may occur in
problem drinkers who are not alcohol dependent. To help understand the
development of ALD, this study used a rodent model to examine differences in
liver damage between binge drinkers and heavy drinkers.
Researchers at UCSF compared the metabolic effects in mice of
repeated binge-like alcohol drinking, a single binge-drinking session, and
repeated moderate alcohol drinking. Several markers of early- and later-stage
liver disruption were examined.
Results indicated that even limited binge-like alcohol
drinking disrupts liver function, which could lead to more severe forms of
liver damage. These findings point to several aspects of early liver
dysfunction seen in humans, including fatty liver, induction of the liver
metabolic enzyme CYP2E1, and increased alcohol metabolism.
The study, funded by the NIH/NIAAA, also demonstrates the
great potential value of preclinical studies for understanding human disorders.
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