Low molecular weight water-soluble Gastrodia elata polysaccharide GEP-2 alleviates DSS-induced ulcerative colitis by enhancing the intestinal barrier, modulating gut microbiota, and suppressing inflammation

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Authors: Na Li, Xingjian Wen, Xuefeng He, Rui Liang, Jiuyu Fan, Dan Liao, Mengting Li, Yongde Wang, Yanfeng Luo
Cited by: 2
References: 41

Abstract

Gastrodia elata Blume, a traditional Chinese herb, exhibits biological activities linked to its polysaccharides. This study isolated a low-molecular-weight, water-soluble polysaccharide, GEP-2, from Gastrodia elata and investigated its protective effect on dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) in mice, focusing on intestinal barrier function, immune response and microbiota regulation. UC was induced in mice via oral administration of 3% DSS for 7 days. Assessments included disease activity index (DAI), colon length, serum cytokines, tight junction proteins (ZO-1, occludin, claudin-1), NF-κB/STAT3 expression, and gut microbiota analysis via 16S rRNA sequencing. It was found that GEP-2, a branched polysaccharide with α-d-glucose as the main chain with substitutions such as GalA, Gal, Rha, and Ara, exhibited broad molecular weight distribution (Mn = 2.54 kDa, Mw = 9.24 kDa). Compared to the DSS model group, GEP-2 significantly reduced DAI scores, weight loss, colon shortening, and pro-inflammatory cytokines (TNF-α, IL-1β, IL-6), while elevating anti-inflammatory IL-10. It enhanced intestinal barrier function by upregulating tight junction proteins and suppressing the NF-κB p65/STAT3 signaling pathway. Results also showed that GEP-2 affects gut microbiota composition, enriching beneficial taxa like Dubosiella, Clostridia UCG-014, and Alistipes. These findings highlight that GEP-2 has potential as a protective agent for UC via microbiota-gut axis regulation.

Fields of Study & Subjects

Biological and pharmacological studies of plants Traditional Chinese Medicine Analysis Gut microbiota and health

Publication details

Journal / source
International Journal of Biological Macromolecules
Publisher
Elsevier BV
Volume
343
Issue
Pt 2
Pages
150385–150385
Publication date
21 January 2026
Language
EN