Abstract | BACKGROUND AND AIMS: METHODS: We perfused the jejunum with a solution with or without MDP, or with a solution of MDP + Gly-Gly and explored the degree of inflammation to determine the role of PepT1-Nod2 signaling pathway in small intestine mucosa. RESULTS: MDP perfusion induced inflammatory cell accumulation and intestinal damage, accompanied by an increase in mucosal Nod2 and Rip2 transcript expression. NFκB activity and inflammatory cytokine expression, including serum levels of TNF-α, IL-1β, and IL-6, increased in the MDP group compared to the controls; these effects were reversed by perfusion of the nutritional dipeptide Gly-Gly. CONCLUSION: MDP can be transported through PepT1, causing inflammatory damage in the rat small intestine. Nod2-Rip2-NFκB signaling involved in the small intestinal inflammatory injury caused by MDP which is transported through PepT1.
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Authors | Guoguang Ma, Bin Shi, Jingquan Liu, Hongze Zhang, Zijun YinTao, Xiaoli Lou, Dongyu Liang, Yanqiang Hou, Shengxia Wan, Wanhua Yang |
Journal | Digestive diseases and sciences
(Dig Dis Sci)
Vol. 60
Issue 11
Pg. 3264-70
(Nov 2015)
ISSN: 1573-2568 [Electronic] United States |
PMID | 26138652
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cytokines
- Inflammation Mediators
- NF-kappa B
- NOD2 protein, rat
- Nod2 Signaling Adaptor Protein
- Peptide Transporter 1
- Slc15a1 protein, rat
- Symporters
- Glycylglycine
- Acetylmuramyl-Alanyl-Isoglutamine
- Receptor-Interacting Protein Serine-Threonine Kinase 2
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Topics |
- Acetylmuramyl-Alanyl-Isoglutamine
(metabolism, toxicity)
- Animals
- Cytokines
(metabolism)
- Enteritis
(chemically induced, enzymology, pathology)
- Glycylglycine
(pharmacology)
- Inflammation Mediators
(metabolism)
- Intestinal Mucosa
(drug effects, enzymology, pathology)
- Jejunum
(drug effects, enzymology, pathology)
- Male
- NF-kappa B
(metabolism)
- Nod2 Signaling Adaptor Protein
(metabolism)
- Peptide Transporter 1
- Rats, Sprague-Dawley
- Receptor-Interacting Protein Serine-Threonine Kinase 2
(metabolism)
- Signal Transduction
(drug effects)
- Symporters
(metabolism)
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