Inflammatory bowel disease (IBD) poses a threat to health and compromises the immune system and gut microflora. The present study aimed to explore the effects of rice protein (RP) purified from rice dregs (RD) on acute colitis induced by dextran sulfate sodium (DSS) and the underlying mechanisms. Results showed that RP treatment could alleviate the loss of body weight, colon shortening and injury, and the level of disease activity index, repair colonic function (claudin-1, ZO-1 and occludin), regulate inflammatory factors, and restore oxidative balance (malondialdehyde (MDA), catalase (CAT), superoxide dismutase (SOD), and total antioxidant capability (T-AOC)) in mice. Also, RP treatment could activate the Kelch-like ECH-associating protein 1 (Keap1)−nuclear factor E2-related factor 2 (Nrf2) signaling pathway, mediate the expression of downstream antioxidant protease (NQO-1, HO-1, and Gclc), regulate gut microbiota by enhancing the relative abundance of Akkermansia and increasing the value of F/B, and adjust short-chain fatty acid levels to alleviate DSS-induced colitis in mice. Thus, RP may be an effective therapeutic dietary resource for ulcerative colitis.
Inflammatory bowel disease (IBD), with increasing incidence,
causes
a range of gastrointestinal symptoms and brings distress and impact
on the health and lives of patients. The aim of this study was to
explore the protective effects of industrially produced rice protein
peptides (RPP) on dextran sulfate sodium (DSS)-induced acute colitis
in mice and the potential mechanisms. The results showed that RPP
treatment alleviated the symptoms of colitis in mice, including weight
loss, colon shortening, and injury, decreased the level of disease
activity index (DAI), regulated the balance of inflammatory factors
and oxidation, activated Kelch-like ECH-associating protein 1 (Keap1)-nuclear
factor E2-related factor 2 (Nrf2) signaling pathway, regulated the
expression of related antioxidant proteases, and promoted the expression
of intestinal tight junction proteins. In addition, RPP maintained
intestinal mucosal barrier function and alleviated acute colitis caused
by DSS treatment in mice by increasing the value of F/B, increasing
the relative abundance of beneficial bacteria such as Akkermansia, and regulating the level of short-chain fatty acids. In conclusion,
RPP alleviated colitis symptoms through the Keap1–Nrf2 signaling
pathway and regulating gut microbiota, which had the potential as
dietary supplements or functional foods.
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