Comparing the effects of acute alcohol consumption in germ-free and conventional mice: the role of the gut microbiota

BMC Microbiol. 2014 Sep 16:14:240. doi: 10.1186/s12866-014-0240-4.

Abstract

Background: Increasing evidence suggest that the gut microbiota plays an important role in liver pathology after acute alcohol intake. The aim of our study was to investigate the roles played by commensal bacteria in alcohol-induced liver injury and in the dysbiosis caused by alcohol intake in germ-free mice, as well as the possibility of protection against alcohol-induced injuries in animals fed a high-fiber diet. For these purposes, germ-free and conventional mice were submitted to acute alcohol intake, consisting of administration of ethanol in their drinking water for 7 days, with a higher dose of alcohol administered on day 7.

Results: There was no liver injury after alcohol consumption, and there was less neutrophil infiltration and lower pro-inflammatory cytokine levels (CXCL-1/KC and interleukin (IL)-6) in the liver in germ-free mice compared with alcohol-fed conventional mice. Additionally, conventionalization of germ-free mice with intestinal contents from alcohol-fed conventional mice induced injury and inflammation in both the liver and the intestine, suggesting that alcohol intake successively caused a perturbation of the intestinal microbiota (dysbiosis) and liver injury. Finally, previous treatment with a high-fiber diet decreased liver injury and gut permeability in alcohol-fed conventional mice.

Conclusions: In conclusion, the results of the present study provide evidence that the gut microbiota plays an important role in alcohol-induced liver injury, apparently through dysbiosis of the intestinal microbial ecosystem caused by alcohol intake. Furthermore, treatment with a high-fiber diet can counteract hepatocyte pathology and gut leakage and thus could be a promising therapeutic option.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Drinking / adverse effects*
  • Animals
  • Chemokine CXCL1 / metabolism
  • Diet, High-Fat
  • Ethanol / adverse effects*
  • Female
  • Germ-Free Life / physiology
  • Inflammation / chemically induced
  • Inflammation / metabolism
  • Inflammation / microbiology
  • Interleukin-6 / metabolism
  • Intestinal Mucosa / metabolism
  • Intestines / microbiology*
  • Liver / metabolism
  • Liver / microbiology
  • Liver / pathology*
  • Liver Diseases / metabolism
  • Liver Diseases / microbiology
  • Liver Diseases / pathology*
  • Mice
  • Microbiota / physiology*
  • Permeability

Substances

  • Chemokine CXCL1
  • Interleukin-6
  • Ethanol