1. A Polysaccharide Isolated from Codonopsis pilosula with Immunomodulation Effects Both In Vitro and In Vivo.
- Author
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Zou YF, Zhang YY, Fu YP, Inngjerdingen KT, Paulsen BS, Feng B, Zhu ZK, Li LX, Jia RY, Huang C, Song X, Lv C, Ye G, Liang XX, He CL, Yin LZ, and Yin ZQ
- Subjects
- Animals, Cell Survival drug effects, Hydrolysis, Immunity, Mucosal drug effects, Immunologic Factors chemistry, Mice, Molecular Structure, Monosaccharides chemistry, Peyer's Patches drug effects, Peyer's Patches immunology, Peyer's Patches metabolism, Plant Extracts chemistry, Polysaccharides chemistry, Spectrum Analysis, Codonopsis chemistry, Immunologic Factors pharmacology, Immunomodulation drug effects, Plant Extracts pharmacology, Polysaccharides pharmacology
- Abstract
In this study, an acidic polysaccharide from Codonopsis pilosula Nannf. var. modesta (Nannf.) L. T. Shen (WCP-I) and its main fragment, WCP-Ia, obtained after pectinase digestion, were structurally elucidated and found to consist of a rhamnogalacturonan I (RG-I) region containing both arabinogalactan type I (AG-I) and type II (AG-II) as sidechains. They both expressed immunomodulating activity against Peyer's patch cells. Endo-1,4-β-galactanase degradation gave a decrease of interleukine 6 (IL-6) production compared with native WCP-I and WCP-Ia, but exo-α-l-arabinofuranosidase digestion showed no changes in activity. This demonstrated that the stimulation activity partly disappeared with removal of β-d-(1→4)-galactan chains, proving that the AG-I side chain plays an important role in immunoregulation activity. WCP-Ia had a better promotion effect than WCP-I in vivo, shown through an increased spleen index, higher concentrations of IL-6, transforming growth factor-β (TGF-β), and tumor necrosis factor-α (TNF-α) in serum, and a slight increment in the secretory immunoglobulin A (sIgA) and CD4
+ /CD8+ T lymphocyte ratio. These results suggest that β-d-(1→4)-galactan-containing chains in WCP-I play an essential role in the expression of immunomodulating activity. Combining all the results in this and previous studies, the intestinal immune system might be the target site of WCP-Ia.- Published
- 2019
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