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Pectic Polysaccharides from Panax ginseng as the Antirotavirus Principals in Ginseng

Authors
Baek, Seung-HoonLee, Jin GyunPark, Seo YoungBae, Ok NamKim, Dong-HyunPark, Jeong Hill
Issue Date
Aug-2010
Publisher
American Chemical Society
Keywords
unclassified drug; IC 50; ginseng; concentration response; drug structure; Viruses; Homogalacturonan; in vitro study; Functional sites; Panax ginseng; Polysaccharides; rhamnogalacturonan; cell adhesion; Rotavirus infection; Hot water extracts; flow cytome
Citation
Biomacromolecules, v.11, no.8, pp.2044 - 2052
Indexed
SCIE
SCOPUS
Journal Title
Biomacromolecules
Volume
11
Number
8
Start Page
2044
End Page
2052
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/39611
DOI
10.1021/bm100397p
ISSN
1525-7797
Abstract
To evaluate the antidiarrheal effect of ginseng, the active principals of ginseng were studied in vitro model of rotavirus infection, the leading cause of severe diarrhea. Two pectic polysaccharides, named as GP50-dHR (56.0 kDa) and GP50-eHR (77.0 kDa), were purified from hot water extract of ginseng by bioassay-linked fractionation. Both polysaccharides rescued cell viability from rotavirus infection dose-dependently (IC50 are 15 and 10 mu g/mL, respectively). Both polysaccharides had common structural features of homogalacturonan backbone with hairy regions of rhamnogalacturonan type I. Arabinose-rich side chains with abundant branch points were unique in GP50-eHR and may contribute to a greater antirotavirus effect of GP50-eHR than GP50-dHR. Because homogalacturonan itself did not show an antirotavirus effect, hairy regions might be functional sites. Of note, the antirotavirus effect of both polysaccharides resulted from inhibiting rotavirus attachment to cells. Together with a wide range of noncytotoxicity, these findings suggest that ginseng polysaccharides are viable therapeutic options for rotavirus diarrhea.
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