Hepatoprotective and antiviral properties of isochlorogenic acid A from Laggera alata against hepatitis B virus infection

被引:73
作者
Hao, Bing-Jie [1 ]
Wu, Yi-Hang [1 ,2 ]
Wang, Jian-Guo [2 ]
Hu, Shao-Qing [1 ]
Keil, Dana Jasmin [3 ]
Hu, Hua-Jun [1 ]
Lou, Ji-Dong [1 ]
Zhao, Yu [4 ]
机构
[1] China Jiliang Univ, Dept Pharm, Zhejiang Prov Key Lab Biometrol & Inspect & Quara, Coll Life Sci, Hangzhou 310018, Peoples R China
[2] Zhejiang Univ, State Key Lab Diag & Treatment Infect Dis, Affiliated Hosp 1, Coll Med, Hangzhou 310003, Zhejiang, Peoples R China
[3] TU Dortmund Univ, Dept Biochem & Chem Engn, D-44227 Dortmund, Germany
[4] Zhejiang Univ, Dept Tradit Chinese Med & Nat Drug Res, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Laggera alata; Isochlorogenic acid A; Anti-hepatitis B virus; Hepatoprotective; Heme oxygenase-1; D-GALACTOSAMINE; SESQUITERPENES; HEPADNAVIRUS; OXYGENASE-1; DERIVATIVES; HEME; RATS; DNA;
D O I
10.1016/j.jep.2012.09.003
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: The aim of this study was to determine the anti-hepatitis B effect of isochlorogenic acid A isolated from Laggera alata (Asteraceae), a traditional Chinese herbal medicine. Materials and methods: The anti-hepatitis B activity of isochlorogenic acid A was evaluated by the D-galactosamine (D-GalN)-induced HL-7702 hepatocyte damage model and the HBV-transfected HepG2.2.15 cells. Results: Isochlorogenic acid A significantly improved HL-7702 hepatocyte viability and markedly inhibited the productions of HBsAg and HBeAg. The inhibitory rates of isochlorogenic acid A on the HBsAg and HBeAg expressions were 86.9% and 72.9%, respectively. In addition, isochlorogenic acid A declined markedly the content of hepatitis B virus covalently closed circular DNA (HBV cccDNA) and induced significantly the heme oxygenase-1 (HO-1) expression in HepG2.2.15 cells. Conclusions: Isochlorogenic acid A was verified to possess the potent anti-hepatitis B activity. The anti-HBV target of isochlorogenic acid A is probably associated with blocking the translation step of the HBV replication. Overexpression of HO-1 may contribute to the anti-HBV activity of isochlorogenic acid A by reducing the stability of the HBV core protein and thus blocking the refill of nuclear HBV cccDNA. Additionally, the hepatoprotective effect of isochlorogenic acid A could be achieved by its antioxidative property and induction of HO-1. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:190 / 194
页数:5
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