4.7 Article

Dietary Polysaccharide from Enteromorpha clathrata Attenuates Obesity and Increases the Intestinal Abundance of Butyrate-Producing Bacterium, Eubacterium xylanophilum, in Mice Fed a High-Fat Diet

Journal

POLYMERS
Volume 13, Issue 19, Pages -

Publisher

MDPI
DOI: 10.3390/polym13193286

Keywords

Enteromorpha clathrata; polysaccharide; obesity; Eubacterium xylanophilum; gut microbiota; prebiotic; gut dysbiosis; probiotic

Funding

  1. National Natural Science Foundation of China [81991522]
  2. National Science and Technology Major Project for Significant New Drugs Development [2018ZX09735004]
  3. Shandong Provincial Major Science and Technology Innovation Project [2018SDKJ0404, 2018SDKJ0401]
  4. Taishan Scholar Climbing Project [TSPD20210304]
  5. Qingdao Postdoctoral Application Research Project Funds

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This study demonstrated the anti-obesity effect of Enteromorpha clathrata polysaccharide (ECP) by reducing body weight and levels of triacylglycerol and cholesterol in high-fat diet (HFD)-fed mice. ECP improved intestinal dysbiosis caused by HFD and reshaped the gut microbiota structure, suggesting its potential as a new prebiotic for treating obesity and associated disorders.
Previous studies have suggested that polysaccharide from Enteromorpha clathrata (ECP) could be used as a potential prebiotic to treat dysbiosis-associated diseases. However, whether it has any therapeutic effects on obesity has not been investigated. In the present study, we explored the anti-obesity effect of ECP and illustrated that it can significantly reduce the body weight and decrease the serum levels of triacylglycerol and cholesterol in high-fat diet (HFD)-fed mice. As revealed by 16S rRNA high-throughput sequencing and bioinformatic analysis, HFD remarkably changed the composition of the gut microbiota and promoted the growth of opportunistic pathogens such as Mucispirillum, Desulfobacterota and Alphaproteobacteria in obese mice. Interestingly, ECP improved intestinal dysbiosis caused by HFD and reshaped the structure of the gut microbiota in diseased mice by increasing the abundance of butyrate-producing bacterium, Eubacterium xylanophilum, in the gut. Altogether, we demonstrate for the first time an anti-obesity effect of ECP and shed new light into its therapeutic mechanisms from the perspective of gut microbiota. Our study will pave the way for the development of ECP as new prebiotic for the treatment of obesity and its associated disorders.

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