Abstract |
Peptides DEDTQAMPFR (DR-10), MLGATSL (ML-7), SLSFASR (SR-7), and MSYSAGF (MF-7) derived from simulated gastrointestinal digestion of preserved egg white (SGD-PEW) exerted anti-inflammatory effects on Caco-2 cells. Here, we aimed to evaluate the anti-inflammatory effects of these peptides derived from SGD-PEW in a mouse model of dextran sodium sulfate (DSS)-induced colitis. The results showed that DR-10, ML-7, SR-7 and MF-7 significantly ameliorated the clinical symptoms of DSS-induced mice colitis, such as weight loss, disease activity index (DAI), colon shortening, spleen hypertrophy and histological scores. Treatment with DR-10, ML-7, SR-7 and MF-7 also significantly inhibited the local secretion of pro-inflammatory cytokines TNF-α and IL-6 and markedly decreased the gene expression of pro-inflammatory cytokines, including TNF-α, IL-6, IL-17, IL-1β, IFN-γ and MCP-1, in DSS-induced mice colitis. Overall, MF-7 showed the best effect of alleviating DSS-induced colitis among the four peptides. These results suggested that MF-7, DR-10, ML-7 and SR-7 may be a potential promising candidate for the treatment of inflammatory bowel disease (IBD).
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Authors | Mengya Zhang , Yan Zhao , Na Wu , Yao Yao , Mingsheng Xu , Huaying Du , Yonggang Tu |
Journal | Food & function
(Food Funct)
Vol. 9
Issue 12
Pg. 6444-6454
(Dec 13 2018)
ISSN: 2042-650X [Electronic] England |
PMID | 30462121
(Publication Type: Journal Article)
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Chemical References |
- Anti-Inflammatory Agents
- Cytokines
- Interleukin-1beta
- Peptides
- Tumor Necrosis Factor-alpha
- Dextran Sulfate
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Topics |
- Animals
- Anti-Inflammatory Agents
(chemistry, metabolism)
- Caco-2 Cells
- Cytokines
(genetics, metabolism)
- Dextran Sulfate
(adverse effects)
- Digestion
- Disease Models, Animal
- Ducks
- Egg White
(chemistry)
- Female
- Humans
- Inflammatory Bowel Diseases
(diet therapy, genetics, metabolism)
- Interleukin-1beta
(genetics, metabolism)
- Mice
- Mice, Inbred BALB C
- Ovum
(chemistry, metabolism)
- Peptides
(chemistry, metabolism)
- Tumor Necrosis Factor-alpha
(genetics, metabolism)
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