Foundry120 atlas

Guar Gum β-Manno-Oligosaccharides Alleviate Ulcerative Colitis in Mice Models <i>via</i> Gut Microflora Modulation

Download from source ↗

Dataset overview

Participants None
Samples None
Reuse readiness 3.6/10 evidence-backed score

Guar Gum β-Manno-Oligosaccharides Alleviate Ulcerative Colitis in Mice Models &lt;i&gt;via&lt;/i&gt; Gut Microflora Modulation.

Abstract

Gut dysbiosis is a key feature in ulcerative colitis, a globally prevalent subtype of inflammatory bowel disease. Microbiota-directed dietary supplements can restore the dysbiotic gut and alleviate ulcerative colitis. We aimed to delineate whether prebiotic guar gum β-manno-oligosaccharides [GG-β-MOS(i) 500 mg/kg, (ii) 1000 mg/kg] favors gut microflora and microflora associated characteristics (MACs) and can prevent dextran sodium sulfate (DSS) induced ulcerative colitis in mice model. DSS challenged adult male C57BL/6 mice were used as model for colon inflammation evaluation. Food and water consumption, disease activity index (DAI), histopathological changes, cytokines in sera and colonic tissues, microflora associated characteristics (MACs; post-fermentation metabolites, short-chain fatty acids, etc.) and gut microflora profiles were studied. We found that GG-β-MOS successfully attenuated colonic inflammation, reduced inflammatory proteins, improved the ratio of Firmicutes to Bacteroidetes and promoted the colonization of probiotics like <i>Lactobacillus</i> and <i>Bifidobacteria</i>. Furthermore, GG-β-MOS enriched beneficial bacteria <i>viz.</i>, <i>Lactobacillus</i>, <i>Bifidobacteria</i>, <i>Bacillus</i> and <i>Enterococcus</i> showed positive correlation with anti-inflammatory metabolites like D-mannose, coprostanol, pentadecane, alpha-linolenic acid, dihomo-γ-linolenic acid, D-ribose, L-fucose, D-arabinose, N-acetyl-D-glucosamine, acetate and butyrate and negative correlation with oxalate, palmitic acid, arachidonic acid and erythritol. Overall, GG-β-MOS supplementation restored altered gut microflora and metabolome leading to improved mucosal repair and reduced intestinal inflammation in DSS induced ulcerative colitis mice model.

Study facts

Organism
—
Platform
—
Age group
adult
Disease groups
—
Anatomical sites
—

Data availability

Specific data assets have not been resolved from the source yet — see the source repository below for the full file listing.

Strengths & limitations for reuse

Limitations

  • Not documented: raw reads are advertised
  • Not documented: feature/otu tables are advertised
  • Not documented: taxonomic tables are advertised
  • Not documented: participant counts are documented
Extraction evidence & provenance

Each extracted field is shown with the source excerpt and location used to resolve it.

Cohort

FieldValueEvidence
cohort.age_group adult
DSS challenged adult male C57BL/6 mice were used as model for colon inflammation evaluation.

Section descriptions[0].description, offset 720

cohort.disease_activity_metadata_available True
disease activity index (DAI), histopathological changes, cytokines in sera and colonic tissues

Section descriptions[0].description, offset 850

Data_Assets

FieldValueEvidence
data_assets.open_access True
Creative Commons Attribution 4.0 International

Section rightsList[0], offset —

Specimens

FieldValueEvidence
specimens.body_site colon inferred
cytokines in sera and colonic tissues, microflora associated characteristics (MACs) ... and gut microflora profiles were studied

Section descriptions[0].description, offset 900

specimens.inflamed_status_available True
were used as model for colon inflammation evaluation

Section descriptions[0].description, offset 740