Antitumor effects of dammarane-type saponins from steamed Notoginseng

被引:15
|
作者
He, Fan [1 ]
Ding, Yan [2 ]
Liang, Chun [3 ]
Song, Seok Bean [4 ]
Dou, De-Qiang [1 ]
Song, Gyu Yong [4 ]
Kim, Young Ho [4 ]
机构
[1] Liaoning Univ Tradit Chinese Med, Dept Pharmacognosy, Dalian, Peoples R China
[2] Dalian Polytech Univ, Inst Chem & Applicat Plant Resources, Dalian, Peoples R China
[3] Korea Inst Oriental Med, Herbal Med Improvement Res Ctr, Taejon, South Korea
[4] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
基金
新加坡国家研究基金会;
关键词
Antitumor; dammarane-type ginsenoside; inhibitory activity; Panax notoginseng; NF-KAPPA-B; PANAX-GINSENG; CELLS;
D O I
10.4103/0973-1296.137372
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Six dammarane-type saponins were extracted from steamed Panax notoginseng. Their chemical structures were identified spectroscopically as ginsenosides Rh-1 (1), Rg(1) (2), 20 (S)-Rg(3) (3), 20 (R)-Rg(3) (4), Rb-3 (5), and Rb-1 (6). Compounds (0.1-10 mu M) were tested for inhibition of tumor necrosis factor-alpha (TNF)-induced nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B) luciferase reporter activity using a human kidney 293T cell-based assay. Ginsenoside Rb-3 (5) showed the most significant activity with an IC50 of 8.2 mu M. This compound also inhibited the induction of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) messenger Ribonucleic acid (mRNA) in a dose-dependent manner after HepG2 cells had been treated with TNF-alpha (10 ng/mL).
引用
收藏
页码:314 / 317
页数:4
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