Cortex periplocae modulates the gut microbiota to restrict colitis and colitis-associated colorectal cancer via suppression of pathogenic Th17 cells - 31/08/22
, Shijun He a, b, ⁎ 
Abstract |
Aberrant microbe-immune cell interaction is a predisposing factor in inflammatory bowel disease (IBD) and colitis-associated cancer (CAC). Cortex Periplocae is a famous traditional Chinese medicine with putative anti-rheumatoid arthritis and anti-dyspepsia effects. Here, we show that the Periploca sepium periplosides (PePs), a cardiac glycosides-free pregnane glycosides extract from root bark of Cortex Periplocae, alleviates colon inflammation, improves intestinal epithelial barrier function, and prevents colitis-associated tumorigenesis in mice with colitis and CAC. Mechanistically, PePs treatment modulates abnormal gut microbiota composition in model mice, especially enriches an anti-inflammatory commensal bacterium A. muciniphila BAA-835. We further demonstrate that the altered gut microbiota following PePs treatment plays an important role in modulation of intestinal Type 17 immunity in both colitis and CAC mouse model. Our results indicate that PePs may be used as a potential gut microbiota modulator to treat IBD and CAC.
Le texte complet de cet article est disponible en PDF.Graphical Abstract |
Highlights |
• | PePs alleviated colitis and CAC in mice. |
• | Protective effects of PePs on colitis and CAC were gut microbiota- and T-cell-dependent. |
• | PePs modulated Type 17 immunity in a gut microbiota-dependent manner. |
• | PePs increased the abundance of anti-inflammatory commensal bacterium A. muciniphila BAA-835. |
Abbreviations : IBD, CD, UC, CRC, CAC, PePs, RRMS, TCM, DSS, DNFB, MLN, AOM, SPF, DAI, TNBS, HPMC, FITC, PCNA, H&E, SDS-PAGE, PNS, ZO-1, PCA, NMDS, LDA, LEfse
Keywords : Colitis, Colitis-associated cancer, Periploca sepium periplosides, Gut microbiota, Intestinal Type 17 immunity
Plan
Vol 153
Article 113399- septembre 2022 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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