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Updated: Sep 12, 2025

Analyzing Beneficial Effects of Nutritional Supplements on Intestinal Epithelial Barrier Functions During Experimental Colitis
Published on: January 5, 2017
Tricobalt tetraselenide nanoparticles improve intestinal barrier function by reshaping the gut microbiota and
Yin Chen1, Na Zhao2, Songling Han1
1State Key Laboratory of Trauma and Chemical Poisoning, Institute of Combined Injury of PLA, College of Preventive Medicine, Army Medical University, Chongqing, 400038, China. wangcheng@tmmu.edu.cn.
Abstract:
The disrupted intestinal mechanical barrier contributes to the pathogenesis of inflammatory bowel disease (IBD) and irradiation-induced intestinal injury (IRIII), both of which lack sufficient medical countermeasures currently. Reshaping the gut microbiota to increase the short-chain fatty acid (SCFA) levels is instrumental for fortifying the mechanical barrier and mitigating these diseases. Inspired by the fact that supplementation of essential trace elements selenium (Se) and cobalt (Co) can enrich SCFA-producing bacteria and promote microbial fermentation, respectively, we prepared tricobalt tetraselenide nanoparticles (Co3Se4 NPs) using a facile biomineralization approach in this study. Oral Co3Se4 NP administration increased intestinal microbial diversity and enriched Alloprevotella, which produced SCFAs, particularly butyric acid (BA), in the gut. Further investigation revealed that BA activated the cell-surface G-protein-coupled receptor 43 (GPR43) in enterocytes and induced protein kinase B (AKT) phosphorylation, resulting in increased expression of the tight junction (TJ) proteins occludin and zonula occludens-1. Accordingly, Co3Se4 NPs ameliorated the gut microbiota dysbiosis and TJ disruption caused by dextran sulfate sodium salt (DSS) and total abdominal γ-ray irradiation, producing a fortified mechanical barrier and alleviating DSS-induced colitis and IRIII in mice. This study demonstrated a biocompatible nanomaterial that can reshape the gut microbiota and fortify epithelial TJs, thereby providing an effective strategy for IBD and IRIII therapies.
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