The effect of Lactobacillus rhamnosus B10 on alcoholic liver injury and intestinal microbiota in alcohol-induced mice model

J Food Biochem. 2022 Oct;46(10):e14372. doi: 10.1111/jfbc.14372. Epub 2022 Aug 5.

Abstract

Lactobacillus rhamnosus B10 (L. rhamnosus B10) isolated from the baby feces was given to an alcohol mice model, aiming to investigate the effects of L. rhamnosus B10 on alcoholic liver injury by regulating intestinal microbiota. C57BL/6N mice were fed with liquid diet Lieber-DeCarli with or without 5% (v/v) ethanol for 8 weeks, and treated with L. rhamnosus B10 at the last 2 weeks. The results showed that L. rhamnosus B10 decreased the serum total cholesterol (1.48 mmol/L), triglycerides (0.97 mmol/L), alanine aminotransferase (26.4 U/L), aspartate aminotransferase (14.2 U/L), lipopolysaccharide (0.23 EU/mL), and tumor necrosis factor-α (138 pg/mL). In addition, L. rhamnosus B10 also reduced the liver triglycerides (1.02 mmol/g prot), alanine aminotransferase (17.8 mmol/g prot) and aspartate aminotransferase (12.5 mmol/g prot) in alcohol mice, thereby ameliorating alcohol-induced liver injury. The changes of intestinal microbiota composition on class, family and genus level in cecum were analyzed. The intestinal symbiotic abundance of Firmicutes was elevated while gram-negative bacteria Proteobacteria and Deferribacteres was decreased in alcohol mice treated with L. rhamnosus B10 for 2 weeks. In summary, this study provided evidence for the therapeutic effects of probiotics on alcoholic liver injury by regulating intestinal flora.

Keywords: L. rhamnosus B10; alcoholic liver injury; intestinal microbiota; microbiota metabolic functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase
  • Animals
  • Aspartate Aminotransferases
  • Cholesterol
  • Disease Models, Animal
  • Ethanol
  • Gastrointestinal Microbiome*
  • Lacticaseibacillus rhamnosus* / physiology
  • Lipopolysaccharides
  • Liver Diseases, Alcoholic* / etiology
  • Liver Diseases, Alcoholic* / pathology
  • Liver Diseases, Alcoholic* / therapy
  • Mice
  • Mice, Inbred C57BL
  • Triglycerides
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Lipopolysaccharides
  • Triglycerides
  • Tumor Necrosis Factor-alpha
  • Ethanol
  • Cholesterol
  • Aspartate Aminotransferases
  • Alanine Transaminase