4.7 Article

Impaired Intestinal Akkermansia muciniphila and Aryl Hydrocarbon Receptor Ligands Contribute to Nonalcoholic Fatty Liver Disease in Mice

Journal

MSYSTEMS
Volume 6, Issue 1, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/mSystems.00985-20

Keywords

microbiome; gut-liver axis; Akkermansia muciniphila; AHR ligands

Categories

Funding

  1. National Key Research and Development Project [2018YFE0110800]
  2. Foshan Core Technology Tackling Key Project [1920001000262]
  3. China Postdoctoral Science Foundation [2019M662893]
  4. National Natural Science Foundation of China [21635006]

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The consumption of saccharin/sucralose alters gut microbial community structure, leading to depletion of Akkermansia muciniphila and development of NAFLD in mice. Metformin or fructo-oligosaccharide supplementation can help restore gut microbiota balance and alleviate NAFLD. A new potential nutritional strategy involves using neohesperidin dihydrochalcone as a substitute for artificial sweeteners and free sugars.
Noncaloric artificial sweeteners (NAS) are extensively introduced into commonly consumed drinks and foods worldwide. However, data on the health effects of NAS consumption remain elusive. Saccharin and sucralose have been shown to pass through the human gastrointestinal tract without undergoing absorption and metabolism and directly encounter the gut microbiota community. Here, we aimed to identify a novel mechanism linking intestinal Akkermansia muciniphila and the aryl hydrocarbon receptor (AHR) to saccharin/sucralose-induced nonalcoholic fatty liver disease (NAFLD) in mice. Saccharin/sucralose consumption altered the gut microbial community structure, with significant depletion of A. muciniphila abundance in the cecal contents of mice, resulting in disruption of intestinal permeability and a high level of serum lipopolysaccharide, which likely contributed to systemic inflammation and caused NAFLD in mice. Saccharin/sucralose also markedly decreased microbiota-derived AHR ligands and colonic AHR expression, which are closely associated with many metabolic syndromes. Metformin or fructo-oligosaccharide supplementation significantly restored A. muciniphila and AHR ligands in sucralose-consuming mice, consequently ameliorating NAFLD. IMPORTANCE Our findings indicate that the gut-liver signaling axis contributes to saccharin/sucralose consumption-induced NAFLD. Supplementation with metformin or fructo-oligosaccharide is a potential therapeutic strategy for NAFLD treatment. In addition, we also developed a new nutritional strategy by using a natural sweetener (neohesperidin dihydrochalcone (NHDC)) as a substitute for NAS and free sugars.

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