Modulatory effects of fermented Polygonatum cyrtonema Hua on immune homeostasis and gut integrity in a dextran-sulfate-sodium-induced colitis model

The gut health-promoting properties of saponin-rich Hua (FP) fermented with P9 were explored in a dextran sulfate sodium (DSS)-induced colitis mouse model. FP supplementation effectively inhibited DSS-induced physiological alteration and impaired immune responses by reducing the disease activity ind...

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Veröffentlicht in:Food & function 2024-03, Vol.15 (6), p.3158-3173
Hauptverfasser: Li, Tao, Yu, Fengyao, Zhang, Tao, Wang, Xiaoya, Sun, Yong, Shuai, Gexia, Chen, Yuhuan, Xue, Yanhua, Zhang, Jinlian, Zhang, Hua
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Sprache:eng
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Zusammenfassung:The gut health-promoting properties of saponin-rich Hua (FP) fermented with P9 were explored in a dextran sulfate sodium (DSS)-induced colitis mouse model. FP supplementation effectively inhibited DSS-induced physiological alteration and impaired immune responses by reducing the disease activity index (DAI) score and restoring the T helper (Th) 1/Th2 and regulatory T (Treg)/Th17 ratios. In addition, FP supplementation protected the gut barrier function against DSS-induced damage upregulation of zonula occludens (ZO)-1 and occludin and downregulation of pro-inflammatory cytokines, including interleukin (IL)-1β, tumor necrosis factor-α (TNF-α), IL-18, and the granulocyte-macrophage colony-stimulating factor (GM-CSF). This study further elucidated the potential mechanisms underlying the FP-mediated suppression of the plasticity of type 3 innate lymphoid cells (ILC3) and subsequent macrophage polarization. Therefore, the FP supplementation effectively restored mucosal immune homeostasis and enhanced gut integrity. In addition, it suppressed the growth of and and promoted the enrichment of probiotics and short-chain fatty acid-producing microbes, such as , , and . In conclusion, Hua fermented with P9 might be a promising dietary intervention to improve gut health by sustaining overall gut homeostasis and related gut integrity.
ISSN:2042-6496
2042-650X
DOI:10.1039/d3fo04556k