Stachyose modulates gut microbiota and alleviates dextran sulfate sodium-induced acute colitis in mice

Saudi J Gastroenterol. 2020 May-Jun;26(3):153-159. doi: 10.4103/sjg.SJG_580_19.

Abstract

Background/aim: Ulcerative colitis (UC) has been implicated to imbalanced enteric flora and reduced microbial diversity. Stachyose is a kind of natural prebiotic which favorably modulate the composition of the gut microbiota. The present study aims to investigate the effects of stachyose on inflammatory levels and gut microbiota of acute colitis mice.

Materials and methods: In this study, the mice were randomly divided into four groups: (1) control group; (2) stachyose group; (3) dextran sulfate sodium (DSS) group; (4) stachyose + DSS group. Hemotoxylin and Eosin (H and E) staining was performed for the distal colon to examine the inflammation and tissue damage. The inflammatory cytokines including IL-6, IL-10, IL-17a, and TNF-α in serum were determined by ELISA assay. The differences in the gut microbiota were analyzed by 16S rDNA gene sequencing.

Results: Histological assay showed that the stachyose treatment significantly reduced the lesions of the colon in DSS-induced colitis. And the upregulated inflammatory cytokines induced by DSS were significantly inhibited by stachyose treatment. Additionally, the sequencing analysis showed that the stachyose changed the gut microbiota composition with a higher level of Akkermansia, as well as selectively increasing some probiotics, including Lactobacillus.

Conclusions: Our results suggested that stachyose increased beneficial microbiota and bacterial diversity to alleviate acute colitis in mice, which might be a new promising option to UC patients.

Keywords: Dextran sulfate sodium; gut microbiota; probiotics; stachyose; ulcerative colitis.

MeSH terms

  • Animals
  • Colitis* / chemically induced
  • Colitis* / drug therapy
  • Colitis* / microbiology
  • Colitis, Ulcerative* / chemically induced
  • Colitis, Ulcerative* / drug therapy
  • Cytokines / metabolism
  • Dextran Sulfate
  • Disease Models, Animal
  • Gastrointestinal Microbiome* / drug effects
  • Inflammation
  • Mice
  • Oligosaccharides* / pharmacology
  • Probiotics

Substances

  • Cytokines
  • Oligosaccharides
  • stachyose
  • Dextran Sulfate