DSPE, a Homogeneous Polysaccharide Purified from Durian
Shell, Ameliorates Ulcerative Colitis by Restoring
Intestinal Epithelial Barrier Function Via the ALG10/AhR/CYP1A1
Signaling Pathways
Xiaotian Xu1#, Leyi Cui1#, Xingshu
Wei1#, Mengmeng Yang1, Renhui Wu1,
Simin Zhang1, Ying Zhang2,
Mohammed Al-Rasheed4, Essam H. Ibrahim5,6,
Shiqi Dong3* and Yuhui Wang1*
1School
of Pharmacy, Guilin Medical University, Guilin 541199,
China; 2College of Veterinary Medicine, China
Agricultural University, Beijing 100193, China; 3College
of Animal Science and Technology, Tarim University, Aral
843300, China; 4Department of Clinical
Sciences, College of Veterinary Medicine, King Faisal
University, Al-Ahsa, P.O. Box 400, 31982, Saudi Arabia;
5Biology Department, Faculty of Science, King
Khalid University, P.O. Box 9004, Abha 61413, Saudi
Arabia; 6Blood Products Quality Control and
Research Department, National Organization for Research
and Control of Biologicals, Cairo, Egypt #These authors
contributed equally to this work and are considered as
co-first authors
Ulcerative colitis (UC) is a chronic idiopathic
inflammatory bowel disease with complex etiology
involving multiple pathological processes including
inflammation and oxidative stress. Traditional Chinese
medicine polysaccharides show promising prospects in
alleviating UC-associated intestinal inflammation but
are mostly derived from high-value economic crops or
medicinal plants at high cost and their high molecular
weights and poor solubility cause low bioavailability,
limiting their development and application. Therefore,
identifying inexpensive alternative polysaccharide
sources with low molecular weight and good water
solubility is key to overcoming these bottlenecks.
Durian shells, agricultural waste rich in pectic
polysaccharides, are widely available at extremely low
cost, making them an ideal candidate. Based on this, we
isolated and purified durian shell polysaccharide
(DSPE), a single component with lower molecular weight
and higher water solubility, from durian shells and
evaluated its therapeutic potential and mechanism in
ameliorating UC using dextran sulfate sodium (DSS)- and
lipopolysaccharide (LPS)-induced models. The results
showed that 20mg/kg DSPE reduced pro-inflammatory
cytokines and oxidative stress, upregulated ZO-1 and
Occludin expression, and restored intestinal epithelial
barrier function both in vivo and in vitro.
Mechanistically, DSPE downregulated ALG10 (asparagine-linked
glycosylation 10) while upregulating AhR (aryl
hydrocarbon receptor) and CYP1A1 (cytochrome P450 family
1 subfamily A member 1). Administration of an AhR
antagonist or ALG10 overexpression aggravated UC
symptoms and attenuated the protective effects of DSPE.
In summary, these findings indicate that DSPE
ameliorates ulcerative colitis by modulating the ALG10/AhR/CYP1A1
signaling pathway to inhibit inflammation and oxidative
stress, thereby restoring intestinal epithelial barrier
integrity.
To Cite This Article:
Xu X, Cui L, Wei X, Yang M, Wu R, Zhang S, Zhang Y, Al-Rasheed
M, Ibrahim EH, Dong S and Wang Y,
2026.
DSPE, a homogeneous polysaccharide purified from durian
shell, ameliorates ulcerative colitis by restoring
intestinal epithelial barrier function via the ALG10/AhR/CYP1A1
signaling pathways.
Pak Vet J, 2026, 46(10): 2336-2351.
http://dx.doi.org/10.29261/pakvetj/2026.249