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Korean Red Ginseng Polysaccharides Enhance Intestinal IgA Production and Barrier Function via Peyer’s Patch Activation in Mice

Authors
 Sung Jin Kim  ;  Hae-Kyung Lee  ;  Ki Sung Kang  ;  Mi-Gi Lee  ;  Myoung-Sook Shin 
Citation
 NUTRIENTS, Vol.16(22) : 3816, 2024-11 
Journal Title
NUTRIENTS
Issue Date
2024-11
MeSH
Animals ; Fatty Acids, Volatile / metabolism ; Feces ; Gastrointestinal Microbiome / drug effects ; Immunoglobulin A* / metabolism ; Intestinal Mucosa / drug effects ; Intestinal Mucosa / metabolism ; Intestine, Small / drug effects ; Intestine, Small / immunology ; Intestine, Small / metabolism ; Male ; Mice ; Panax* / chemistry ; Peyer's Patches* / drug effects ; Peyer's Patches* / immunology ; Peyer's Patches* / metabolism ; Plant Extracts / pharmacology ; Polysaccharides* / pharmacology
Keywords
IgA ; Korean red ginseng ; Peyer’s patches ; intestinal immune modulating
Abstract
Background: Natural products are gaining attention for their potential benefits in gastrointestinal health. Plant-derived polysaccharides are essential for boosting intestinal immunity and maintaining gut homeostasis. This study investigated the effects of Korean red ginseng polysaccharides (KRG-P) on intestinal homeostasis including IgA and SCFA production and mucosal barrier integrity. Methods: Mice were orally administered KRG-P at doses of 50 mg/kg or 200 mg/kg for 10 days. Fecal IgA levels were measured on days 3, 5, and 11 and IgA from cultured Peyer's patch cells from KRG-P-treated mice were analyzed. Additionally, mRNA and protein expression levels of α-defensin, lysozyme, and E-cadherin in the small intestine were examined. Short-chain fatty acids (SCFAs) content in the cecum was also assessed. Results: KRG-P-treated groups showed a significant increase in fecal IgA levels on days 5 and 11, with no notable change on day 3. Cultured Peyer's patch cells from mice demonstrated heightened IgA production. Additionally, KRG-P administration upregulated α-defensin and lysozyme mRNA expression, along with elevated protein expression of E-cadherin, α-defensin, and lysozyme, in the small intestine. KRG-P treatment also led to increased cecal SCFA levels, including acetate, butyrate, and propionate. Conclusions: KRG-P may promote intestinal homeostasis and host defense mechanisms by activating immune cells in Peyer's patches, stimulating IgA production, enhancing antimicrobial peptide expression, and modulating gut microbiota metabolism through increased SCFA production.
Files in This Item:
T992024907.pdf Download
DOI
10.3390/nu16223816
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Lee, Hae-Kyung(이해경)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/202433
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