Identification of natural compounds with anti-hepatitis B virus activity from Rheum palmatum L. ethanol extract

被引:53
作者
Li, Zhi [1 ]
Li, Li-Jun
Sun, Yan
Li, Jing
机构
[1] Shaanxi Normal Univ, Coll Life Sci, Xian, Shaanxi, Peoples R China
[2] Univ Hong Kong, Inst Mol Biol, Hong Kong, Hong Kong, Peoples R China
[3] Jimei Univ, Bioengn Inst, Xiamen, Fujian, Peoples R China
[4] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
[5] Xiangfan Cent Hosp, Dept Infect Dis, Xiangfan, Hubei, Peoples R China
关键词
hepatitis B virus; Rheum palmatum L; anthraquinone;
D O I
10.1159/000107690
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Hepatitis B virus (HBV) infection is a severe health problem in the world; however, there is still no satisfactory therapeutic strategy for the HBV infection. In search for new anti-HBV agents with higher efficiency and less side effects, the anti-HBV activities of traditional Chinese medicine Rheum palmatum L. ethanol extract (RPE) and isolated anthraquinones were evaluated. Methods: The anti-HBV activities of RPE and isolated anthraquinones were demonstrated in a stable HBV-producing cell line HepG2 2.2.15 by using real-time polymerase chain reaction (PCR), enzyme-linked immunosorbent assay (ELISA) and Southern blot analysis. Results: RPE could inhibit HBV-DNA production and HBsAg expression in a dose-dependent manner. The concentration of 50% HBV-DNA inhibition (IC50) of RPE was calculated at 212.36 +/-11 mu g/ml. Six anthraquinones were isolated from RPE by using RP-HPLC. Five free anthraquinones showed weakly or slightly inhibitory activities against HBV. The only combined anthraquinone chrysophanol 8-O-beta-D-glucoside exhibited significant activity against HBV DNA production and antigens expression with an IC50 value of 36.98 +/-8 2.28 mu g/ml on HBV DNA inhibition. Endogenous HBV DNA polymerase activity assay indicated that chrysophanol 8-O-beta-D-glucoside might be a potential inhibitor of the HBV DNA polymerase. Conclusions: The results suggested that RPE could effectively inhibit HBV. The combined anthraquinone chrysophanol 8-O-beta-D-glucoside is the major active compound in RPE and could be a promising candidate for the development of new anti-HBV drugs in the treatment of HBV infection. Copyright (C) 2007 S. Karger AG, Basel.
引用
收藏
页码:320 / 326
页数:7
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