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Analyzing Beneficial Effects of Nutritional Supplements on Intestinal Epithelial Barrier Functions During Experimental Colitis
Published on: January 5, 2017
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Mannose ameliorates experimental colitis by protecting intestinal barrier integrity.
Lijun Dong1,2,3, Jingwen Xie2,3, Youyi Wang2,3
1The Fifth Affiliated Hospital, Southern Medical University, Guangzhou, Guangdong, 510900, China.
Nature Communications
|August 16, 2022
Summary
Mannose supplementation shows promise for treating inflammatory bowel disease (IBD). This study found elevated mannose levels in IBD patients and demonstrated mannose
Area of Science:
- Gastroenterology and Immunology
- Metabolomics
- Molecular Biology
Background:
- Metabolite alterations are implicated in inflammatory bowel disease (IBD) pathogenesis.
- Mannose, a monosaccharide, possesses anti-inflammatory and anti-oxidative properties.
- Elevated circulating mannose levels are observed in IBD patients and experimental colitis models.
Purpose of the Study:
- To investigate the therapeutic potential of mannose in colitis models.
- To elucidate the mechanisms underlying mannose's protective effects on the intestinal barrier.
Main Methods:
- Assessment of circulating mannose levels in IBD patients and colitis mouse models.
- Administration of mannose in dextran sodium sulfate (DSS)-induced and IL-10-deficient spontaneous colitis models.
- Analysis of lysosomal integrity, cathepsin B release, mitochondrial function, and tight junction integrity.
- Evaluation of synergistic effects with mesalamine.
Main Results:
- Mannose treatment attenuated intestinal barrier damage in both colitis models.
- Mannose enhanced lysosomal integrity, limited cathepsin B release, and prevented mitochondrial dysfunction.
- Mannose inhibited myosin light chain kinase (MLCK)-induced tight junction disruption.
- Mannose demonstrated a synergistic therapeutic effect with mesalamine.
Conclusions:
- Mannose supplementation may offer a therapeutic strategy for colitis and related conditions.
- Mannose protects the intestinal barrier by preserving lysosomal and mitochondrial integrity.
- Mannose's mechanisms involve mitigating MLCK-induced tight junction disruption.

