Chemical Diversity of Panax ginseng, Panax quinquifolium, and Panax notoginseng

被引:282
作者
Kim, Dong-Hyun [1 ,2 ]
机构
[1] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, Seoul 130701, South Korea
[2] Kyung Hee Univ, Dept Pharmaceut Sci, Seoul 130701, South Korea
关键词
Panax ginseng; Panax quinquifolium; Panax notoginseng; Constituents; Biotransformation; DAMMARANE-TYPE SAPONINS; ALPHA-L-ARABINOFURANOSIDASE; HUMAN INTESTINAL BACTERIA; CHINESE CRUDE DRUGS; KINASE-A PATHWAY; AMERICAN GINSENG; COMPOUND-K; FLOWER-BUDS; HYPOGLYCEMIC ACTIVITY; TRITERPENE SAPONINS;
D O I
10.5142/jgr.2012.36.1.1
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The major commercial ginsengs are Panax ginseng Meyer (Korean ginseng), P quinquifolium L. (American ginseng), and P notoginseng (Burk.) Chen (Notoginseng). P ginseng is the most commonly used as an adaptogenic agent and has been shown to enhance physical performance, promote vitality, increase resistance to stress and aging, and have immunomodulatory activity. These ginsengs contain saponins, which can be classified as dammarane-type, ocotillol-type and oleanane-type oligoglycosides, and polysaccharides as main constituents. Dammarane ginsenosides are transformed into compounds such as the ginsenosides Rg(3), Rg(5), and Rk(1), by steaming and heating and are metabolized into metabolites such as compound K, ginsenoside Rh-1, proto- and panaxatriol by intestinal microflora. These metabolites are nonpolar, pharmacologically active and easily absorbed from the gastrointestinal tract. However, the activities metabolizing these constituents into bioactive compounds differ significantly among individuals because all individuals possess characteristic indigenous strains of intestinal bacteria. To overcome this difference, ginsengs fermented with enzymes or microbes have been developed.
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页码:1 / 15
页数:15
相关论文
共 150 条
[21]  
Choo MK, 2003, PLANTA MED, V69, P518, DOI 10.1055/s-2003-40653
[22]   Simultaneous determination of ginsenosides and polyacetylenes in American ginseng root (Panax quinquefolium L.) by high-performance liquid chromatography [J].
Christensen, Lars P. ;
Jensen, Martin ;
Kidmose, Ulla .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (24) :8995-9003
[23]   Two new dammarane triterpene glycosides from the rhizomes of Panax notoginseng [J].
Cui, Xiu-Ming ;
Jiang, Zhi-Yong ;
Zeng, Jiang ;
Zhou, Jia-Ming ;
Chen, Ji-Jun ;
Zhang, Xue-Mei ;
Xu, Luo-Shan ;
Wang, Qiang .
JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2008, 10 (09) :845-849
[24]   Six new dammarane-type triterpene saponins from leaves of Panax ginseng [J].
Dou, DQ ;
Chen, YJ ;
Liang, LH ;
Pang, FG ;
Shimizu, N ;
Takeda, T .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2001, 49 (04) :442-446
[25]   Changes in neutral and malonyl ginsenosides in American ginseng (Panax quinquefolium) during drying, storage and ethanolic extraction [J].
Du, XW ;
Wills, RBH ;
Stuart, DL .
FOOD CHEMISTRY, 2004, 86 (02) :155-159
[26]  
Garriques S.S., 1854, ANN CHEM PHARM, V90, P231, DOI [DOI 10.1002/JLAC18540900216, 10.1002/jlac18540900216]
[27]   Compound K enhances insulin secretion with beneficial metabolic effects in db/db mice [J].
Han, Gi Cheol ;
Ko, Sung Kwon ;
Sung, Jong Hwan ;
Chung, Sung Hyun .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (26) :10641-10648
[28]   Ginsenoside 20(S)-protopanaxatriol (PPT) activates peroxisome proliferator-activated receptor γ (PPARγ) in 3T3-L1 adipocytes [J].
Han, KL ;
Jung, MH ;
Sohn, JH ;
Hwang, JK .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (01) :110-113
[29]  
HU S, 1995, VET RES, V26, P155
[30]   New triterpenoid from Panax ginseng exhibits cytotoxicity through p53 and the caspase signaling pathway in the HepG2 cell line [J].
Huang, Jian ;
Tang, Xiao-hui ;
Ikejima, Takashi ;
Sun, Xiu-jia ;
Wang, Xiao-bo ;
Xi, Rong-gang ;
Wu, Li-jun .
ARCHIVES OF PHARMACAL RESEARCH, 2008, 31 (03) :323-329