MDG-1, an Ophiopogon polysaccharide, regulate gut microbiota in high-fat diet-induced obese C57BL/6 mice

Lin-lin Shi1, Yuan Li1, Yuan Wang1

  • 1Engineering Research Center of Modern Preparation Technology of TCM, Ministry of Education, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, PR China.

Insights

MDG-1, a fructan from Ophiopogon japonicus, aids weight loss by altering gut microbiota. This indigestible compound is fermented by gut bacteria, which then provide beneficial metabolites to the host, promoting health.

Area of Science:

  • Microbiology
  • Nutrition Science
  • Metabolomics

Background:

  • Plant polysaccharides require microbial fermentation for host assimilation.
  • MDG-1, a β-d-fructan from Ophiopogon japonicus, shows anti-obesity and hypoglycemic effects but poor absorption.
  • The mechanism of MDG-1's efficacy via gut microbiota regulation is not fully understood.

Purpose of the Study:

  • To investigate the impact of MDG-1 on gut microbiota structure in obese mice.
  • To determine the metabolic consequences of MDG-1 on specific gut bacteria.
  • To elucidate how MDG-1 exerts its beneficial effects through gut microbiota interaction.

Main Methods:

  • Obese mice fed a high-fat diet were treated with MDG-1 (300mg/kg) or vehicle for 12 weeks.
  • Fecal gut microbiota structure was analyzed using pyrosequencing.
  • Dominant bacteria were cultured with MDG-1 in vitro, and their metabolic profiles were analyzed using metabonomics.

Main Results:

  • MDG-1 treatment decreased the Firmicutes/Bacteroidetes ratio, normalizing gut microbiota.
  • MDG-1 altered the metabolic profiles of gut bacteria.
  • Indigestible MDG-1 was utilized by gut microbiota, producing host-assimilable metabolites.

Conclusions:

  • MDG-1 effectively modulates gut microbiota composition and function in obese mice.
  • Gut microbiota fermentation of MDG-1 contributes to its anti-obesity, metabolic, and immune-boosting effects.
  • MDG-1 represents a promising prebiotic for managing obesity and metabolic dysfunction through gut microbiota manipulation.

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