Antioxidant and anti-tumor promoting activities of the methanol extract of heat-processed ginseng

被引:299
作者
Keum, YS
Park, KK
Lee, JM
Chun, KS
Park, JH
Lee, SK
Kwon, H
Surh, YJ [1 ]
机构
[1] Seoul Natl Univ, Res Inst Pharmaceut Sci, Coll Pharm, Seoul 151742, South Korea
[2] Yonsei Univ, Coll Dent, Seoul 120752, South Korea
[3] Seoul Natl Univ, Dept Food Sci & Nutr, Coll Human Ecol, Seoul 151742, South Korea
关键词
ginseng; antioxidant; anti-tumor promotion; mouse skin carcinogenesis; ornithine decarboxylase;
D O I
10.1016/S0304-3835(99)00369-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Heat treatment of Panax ginseng C.A. Meyer at a temperature higher than that applied to the conventional preparation of red ginseng yielded a mixture of saponins with potent antioxidative properties. Thus, the methanol extract of heat-processed neo-ginseng (designated as 'NGMe') attenuated lipid peroxidation in rat brain homogenates induced by ferric ion or ferric ion plus ascorbic acid. Furthermore, the extract protected against strand scission in empty set X174 supercoiled DNA induced by UV photolysis of H2O2, and was also capable of scavenging superoxide generated by xanthine-xanthine oxidase or by 12-O-tetradecanoylphorbol-13-acetate (TPA) in differentiated human promyelocytic leukemia (HL-60) cells. Topical application of NGMe onto shaven backs of female ICR mice 10 min prior to TPA, significantly ameliorated skin papillomagenesis initiated by 7,12-dimethylbenz[a]anthracene. Moreover, TPA-induced enhancement of epidermal ornithine decarboxylase (ODC) activity and ODC mRNA expression was abolished by a topical dose (0.68 mg) of NGMe. Likewise, TPA-induced production of tumor necrosis factor- in mouse skin was inhibited by NGMe pretreatment. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:41 / 48
页数:8
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