Pectic Polysaccharides from Panax ginseng as the Antirotavirus Principals in Ginseng

被引:63
作者
Baek, Seung-Hoon [1 ,2 ]
Lee, Jin Gyun [1 ,2 ]
Park, Seo Young [1 ,2 ]
Bae, Ok Nam [3 ,4 ]
Kim, Dong-Hyun [5 ]
Park, Jeong Hill [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Seoul Natl Univ, Pharmaceut Sci Res Inst, Seoul 151742, South Korea
[3] Michigan State Univ, Dept Neurol, E Lansing, MI 48824 USA
[4] Michigan State Univ, Dept Ophthalmol, E Lansing, MI 48824 USA
[5] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, Coll Pharm, Seoul 130701, South Korea
关键词
CELL-CYCLE ARREST; ACIDIC POLYSACCHARIDES; ROTAVIRUS VACCINES; ANTIVIRAL ACTIVITY; METHYLATION; INDUCTION; FEATURES; BINDING; PLANT; ASSAY;
D O I
10.1021/bm100397p
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:2044 / 2052
页数:9
相关论文
共 44 条
[1]
Abad FX, 1998, APPL ENVIRON MICROB, V64, P2392
[2]
The immunomodulator ginsan induces resistance to experimental sepsis by inhibiting Toll-like receptor-mediated inflammatory signals [J].
Ahn, JY ;
Choi, IS ;
Shim, JY ;
Yun, EK ;
Yun, YS ;
Jeong, GJ ;
Song, JY .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2006, 36 (01) :37-45
[3]
Rotavirus vaccines: viral shedding and risk of transmission [J].
Anderson, Evan J. .
LANCET INFECTIOUS DISEASES, 2008, 8 (10) :642-649
[4]
Development of a rapid and sensitive quantitative assay for rotavirus based on flow cytometry [J].
Barardi, CRM ;
Emslie, KR ;
Vesey, G ;
Williams, KL .
JOURNAL OF VIROLOGICAL METHODS, 1998, 74 (01) :31-38
[5]
Conformational and configurational features of acidic polysaccharides and their interactions with calcium ions:: a molecular modeling investigation [J].
Braccini, I ;
Grasso, RP ;
Pérez, S .
CARBOHYDRATE RESEARCH, 1999, 317 (1-4) :119-130
[6]
A 96-well assay for uronic acid carbazole reaction [J].
Cesaretti, M ;
Luppi, E ;
Maccari, F ;
Volpi, N .
CARBOHYDRATE POLYMERS, 2003, 54 (01) :59-61
[7]
In vitro antiviral activity of marine sponges collected off Brazilian coast [J].
da Silva, AC ;
Kratz, JM ;
Farias, FM ;
Henriques, AT ;
dos Santos, J ;
Leonel, RM ;
Lerner, C ;
Mothes, B ;
Barardi, CRM ;
Simòes, CMO .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (01) :135-140
[8]
Rotavirus vaccines: an overview [J].
Dennehy, Penelope H. .
CLINICAL MICROBIOLOGY REVIEWS, 2008, 21 (01) :198-+
[9]
Structural characterization and immunological activity of two cold-water extractable polysaccharides from Cistanche deserticola Y. C.!Ma [J].
Dong, Qun ;
Yao, Han ;
Fang, Ji-nian ;
Ding, Kan .
CARBOHYDRATE RESEARCH, 2007, 342 (10) :1343-1349
[10]
The rhesus rotavirus VP4 sialic acid binding domain has a galectin fold with a novel carbohydrate binding site [J].
Dormitzer, PR ;
Sun, ZYJ ;
Wagner, G ;
Harrison, SC .
EMBO JOURNAL, 2002, 21 (05) :885-897