4.7 Article

Marine Chitooligosaccharide Alters Intestinal Flora Structure and Regulates Hepatic Inflammatory Response to Influence Nonalcoholic Fatty Liver Disease

Journal

MARINE DRUGS
Volume 20, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/md20060383

Keywords

marine chitooligosaccharide; nonalcoholic fatty liver disease; intestinal flora; LPS/TLR4/NF-kappa B inflammatory pathway; short-chain fatty acid

Funding

  1. Science and Technology Program of Guangzhou, China [202103000089]
  2. Guangdong Demonstration Base for Joint Cultivation of Postgraduates (2019)
  3. Science Foundation for Distinguished Young Scholars of Guangdong [2020B1515020026]
  4. National Natural Science Foundation of China [21804025]

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In this study, oral administration of marine chitooligosaccharide COSM significantly improved the imbalance of intestinal flora and inflammatory response in a mouse model of hepatic steatosis induced by a high-fat, high-sugar diet, thereby alleviating intrahepatic lipid accumulation.
In this study, C57BL/6 mice were given an HFHSD diet for 8 weeks to induce hepatic steatosis and then given COSM solution orally for 12 weeks. The study found that the HFHSD diet resulted in steatosis and insulin resistance in mice. The formation of NAFLD induced by HFHSD diet was related to the imbalance of intestinal flora. However, after COSM intervention, the abundance of beneficial bacteria increased significantly, while the abundance of harmful bacteria decreased significantly. The HFHSD diet also induced changes in intestinal bacterial metabolites, and the content of short-chain fatty acids in cecal contents after COSM intervention was significantly higher than that in the model group. In addition, COSM not only improved LPS levels and barrier dysfunction in the ileum and colon but upregulated protein levels of ZO-1, occludin, and claudin in the colon and downregulated the liver LPS/TLR4/NF-kappa B inflammatory pathway. We concluded that the treatment of marine chitooligosaccharide COSM could improve the intestinal microflora structure of the fatty liver and activate an inflammatory signaling pathway, thus alleviating the intrahepatic lipid accumulation induced by HFHSD.

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