Protocatechuic aldehyde inhibits hepatitis B virus replication both in vitro and in vivo

被引:90
作者
Zhou, Zhe
Zhang, Yi
Ding, Xiao-Ran
Chen, Su-Hong
Yang, Jing
Wang, Xue-Jun
Jia, Gao-Long
Chen, Hong-Shan
Bo, Xiao-Chen
Wang, Sheng-Qi
机构
[1] Beijing Inst Radiat Med, Beijing 100850, Peoples R China
[2] Peking Union Med Coll, Inst Med Biotechnol, Chinese Acad Med Sci, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
protocatechuic aldehyde; duck hepatitis B virus; hepatitis B virus; Salvia miltiorrhiza;
D O I
10.1016/j.antiviral.2006.12.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Natural compounds provide a large reservoir of potentially active anti-hepatitis B virus (HBV) agents. We examined the direct effects of protocatechuic aldehyde (PA; derived from the Chinese herb, Salvia miltiorrhiza) on HBV replication in HepG2 2.2.15 cell line and duck hepatitis B virus (DHBV) replication in ducklings in vivo. The extracellular HBV DNA, hepatitis B e antigen (HBeAg) and hepatitis B surface antigen (HBsAg) concentrations in cell culture medium were determined by quantitative real-time PCR and ELISA, respectively. DHBV in duck serum was analyzed by dot blot. PA appeared to downregulate the secretion of Hl3sAg and HBeAg as well as the release of HBV DNA from HepG2 2.2.15 in a dose- and time-dependent manner at concentrations between 24 and 48 mu g/mL. PA (25, 50, or 100 mg/kg, intraperitoneally, twice daily) also reduced viremia in DHBV-infected ducks. We provide the first evidence that PA, a novel anti-HBV substance derived from traditional Chinese herb S. miltiorrhiza, can efficiently inhibits HBV replication in HepG2 2.2.15 cell line in vitro and inhibit DHBV replication in ducks in vivo. PA therefore warrants further investigation as a potential therapeutic agent for HBV infections. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 64
页数:6
相关论文
共 24 条
[1]   The liver in traditional Chinese medicine [J].
Chen, TSN ;
Chen, PSY .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1998, 13 (04) :437-442
[2]   Organ and species specificity of hepatitis B virus (HBV) infection: A review of literature with a special reference to preferential attachment of HBV to human hepatocytes [J].
DeMeyer, S ;
Gong, ZJ ;
Suwandhi, W ;
vanPelt, J ;
Soumillion, A ;
Yap, SH .
JOURNAL OF VIRAL HEPATITIS, 1997, 4 (03) :145-153
[3]   Herbal medicines for liver diseases [J].
Dhiman, RK ;
Chawla, YK .
DIGESTIVE DISEASES AND SCIENCES, 2005, 50 (10) :1807-1812
[4]   INHIBITION OF THE REPLICATION OF HEPATITIS-B VIRUS INVITRO BY 2',3'-DIDEOXY-3'-THIACYTIDINE AND RELATED ANALOGS [J].
DOONG, SL ;
TSAI, CH ;
SCHINAZI, RF ;
LIOTTA, DC ;
CHENG, YC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8495-8499
[6]   RAPID RESOLUTION OF DUCK HEPATITIS-B VIRUS-INFECTIONS OCCURS AFTER MASSIVE HEPATOCELLULAR INVOLVEMENT [J].
JILBERT, AR ;
WU, TT ;
ENGLAND, JM ;
HALL, PD ;
CARP, NZ ;
OCONNELL, AP ;
MASON, WS .
JOURNAL OF VIROLOGY, 1992, 66 (03) :1377-1388
[7]  
KANE M, 1995, VACCINE, V13, pS47
[8]   A CELL-CULTURE ASSAY FOR COMPOUNDS WHICH INHIBIT HEPATITIS-B VIRUS-REPLICATION [J].
KORBA, BE ;
MILMAN, G .
ANTIVIRAL RESEARCH, 1991, 15 (03) :217-228
[9]   INVITRO AND INVIVO COMPARISON OF THE ABILITIES OF PURINE AND PYRIMIDINE 2',3'-DIDEOXYNUCLEOSIDES TO INHIBIT DUCK HEPADNAVIRUS [J].
LEE, B ;
LUO, WX ;
SUZUKI, S ;
ROBINS, MJ ;
TYRRELL, DLJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (03) :336-339
[10]   VIRUS OF PEKIN DUCKS WITH STRUCTURAL AND BIOLOGICAL RELATEDNESS TO HUMAN HEPATITIS-B VIRUS [J].
MASON, WS ;
SEAL, G ;
SUMMERS, J .
JOURNAL OF VIROLOGY, 1980, 36 (03) :829-836