Alcohol consumed during just seven weeks of intermittent binge consumption harms the liver in ways that more moderate daily alcohol use does not, according to researchers at UC San Francisco…


Scott A. Wegner, Katherine A. Pollard, Viktor Kharazia, David Darevsky, Luz Perez, Sanjoy Roychowdhury, Allison Xu, Dorit Ron, Laura E. Nagy, Frederic Woodward Hopf:


Wegner, S. A., Pollard, K. A., Kharazia, V., Darevsky, D., Perez, L., Roychowdhury, S., Xu, A., Ron, D., Nagy, L. E. and Hopf, F. W. (2017), Limited Excessive Voluntary Alcohol Drinking Leads to Liver Dysfunction in Mice. Alcohol Clin Exp Res. doi:10.1111/acer.13303

Alcoholism Clinical and Experimental Research
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Original Article

Limited Excessive Voluntary Alcohol Drinking Leads to Liver Dysfunction in Mice



Liver damage is a serious and sometimes fatal consequence of long-term alcohol intake, which progresses from early-stage fatty liver (steatosis) to later-stage steatohepatitis with inflammation and fibrosis/necrosis. However, very little is known about earlier stages of liver disruption that may occur in problem alcohol users, those who consume excessively but are not dependent on alcohol.


The researchers examined how repeated binge-like alcohol consumption in C57BL/6 mice altered liver function, as compared with a single binge-intake session and with repeated moderate alcohol consumption. The researchers measured a number of markers associated with early- and later-stage liver disruption, including liver steatosis, measures of liver cytochrome P4502E1 (CYP2E1) and alcohol dehydrogenase (ADH), alcohol metabolism, expression of cytokine mRNA, accumulation of 4-hydroxynonenal (4-HNE) as an indicator of oxidative stress, and alanine transaminase/aspartate transaminase as a measure of hepatocyte injury.


Importantly, repeated binge-like alcohol consumption increased triglyceride levels in the liver and plasma, and increased lipid droplets in the liver, indicators of steatosis. In contrast, a single binge-intake session or repeated moderate alcohol consumption did not alter triglyceride levels.

In addition, alcohol exposure can increase rates of alcohol metabolism through CYP2E1 and ADH, which can potentially increase oxidative stress and liver dysfunction. Intermittent, excessive alcohol intake increased liver CYP2E1 mRNA, protein, and activity, as well as ADH mRNA and activity.

Furthermore, repeated, binge-like alcohol consumption, but not a single binge or moderate alcohol use, increased alcohol metabolism.

Finally, repeated, excessive intake transiently elevated mRNA for the proinflammatory cytokine IL-1B and 4-HNE levels, but did not alter markers of later-stage liver hepatocyte injury.


Together, the researchers provide data suggesting that even relatively limited binge-like alcohol use can lead to disruptions in liver function, which might facilitate the transition to more severe forms of liver damage.

Source Website: Alcoholism Clinical and Experimental Research