1. Academic Validation
  2. Structural characterization of a water-soluble α-D-glucan from Crepis lignea roots and its alleviation of DSS-induced ulcerative colitis in Drosophila melanogaster

Structural characterization of a water-soluble α-D-glucan from Crepis lignea roots and its alleviation of DSS-induced ulcerative colitis in Drosophila melanogaster

  • Bioorg Chem. 2026 Jun 15:174:109726. doi: 10.1016/j.bioorg.2026.109726.
Qian Zhang 1 Wenyu Wang 2 Chenhan Wu 3 Qingting Du 3 Weili Yin 3 Jiaheng Chen 4 Jian Ma 2 Chong Li 5 Shaojie Zhang 6
Affiliations

Affiliations

  • 1 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, PR China. Electronic address: [email protected].
  • 2 Department of Urology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, PR China.
  • 3 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, PR China.
  • 4 Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, PR China.
  • 5 College of Life Sciences, Shandong Agricultural University, Tai'an 271018, PR China. Electronic address: [email protected].
  • 6 Guangdong Provincial Key Laboratory of Research and Development of Natural Drugs, School of Pharmacy, Guangdong Medical University, Dongguan 523808, China. Electronic address: [email protected].
Abstract

Ulcerative colitis (UC) is characterized by recurrent inflammation of the gastrointestinal tract, and currently available treatment drugs are limited. Plant-derived Polysaccharides hold promise for UC prevention. A water-soluble α-D-glucan (CLP80-1) with a molecular weight of 8.17 × 105 Da was isolated and characterized from the roots of traditional Chinese medicinal plant Crepis lignea. Structural analysis revealed that its repeating units comprise →6)-α-D-Glcp-(1 → and →3,6)-α-D-Glcp-(1 → residues as the backbone, with α-D-Glcp-(1 → as side chains substituted at C-3. The protective effects of CLP80-1 on dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) in Drosophila melanogaster were investigated. Our results demonstrated that treatment with 1% CLP80-1 significantly improved survival rates, attenuated gut atrophy, reduced intestinal permeability, enhanced intestinal barrier function, suppressed excessive proliferation of intestinal stem cells (ISCs) and enteroblasts (EBs), and inhibited the death of intestinal epithelial cells (IECs). Metabolomic and transcriptomic analyses revealed that CLP80-1 mainly affected amino acid metabolism, TCA cycle, Oxidative Phosphorylation and JAK/STAT signaling pathway. Furthermore, CLP80-1 reduced Reactive Oxygen Species (ROS) levels, suppressed the expression of pro-inflammatory factors, and downregulated the JAK-STAT signaling pathway, thereby mitigating oxidative stress and inflammatory responses. These findings suggest that CLP80-1 is effective in alleviating intestinal inflammation and may serve as a promising therapeutic candidate for addressing gut inflammatory conditions.

Keywords

Drosophila melanogaster; Ulcerative colitis; α-D-glucan.

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