Cytotoxicity and anti-hepatitis B virus activities of saikosaponins from Bupleurum species

被引:67
作者
Chiang, LC
Ng, LT
Liu, LT
Shieh, DE
Lin, CC
机构
[1] Kaohsiung Med Univ, Coll Pharm, Grad Inst Pharmaceut Sci, Kaohsiung 807, Taiwan
[2] Kaohsiung Med Univ, Grad Inst Med, Kaohsiung, Taiwan
[3] Tajen Inst Technol, Fac Food Sci & Technol, Pingtung, Taiwan
[4] Kaohsiung Med Univ, Coll Med, Dept Microbiol, Kaohsiung 807, Taiwan
关键词
saikosaponins; HBV; hepatoma; apoptosis; Hep G2.2.15 cells; Bupleurum spec; Umbelliferae;
D O I
暂无
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Saikosaponins, the main active constituents of Bupleurum spp., have been shown to possess immunomodulatory, hepatoprotective, anti-tumor and anti-viral activities. In this study, saikosaponins a, c and d were evaluated for cytotoxicity and anti-hepatitis B virus (HBV) activities. Results showed that, with the exception of saikosaponins a and d, HBV-transfected human hepatoma cells (2.2.15 cells) cultured with saikosaponin c showed a significantly lower level of HBeAg in culture medium. Saikosaponin c also possessed activity in inhibiting HBV DNA replication; this inhibitory effect was not due to the cytotoxicity of saikosaponin c or its effect on 2.2.15 cell proliferation. Although saikosaponin d exhibited cytotoxicity on 2.2.15 cells, it failed to inhibit HBV multiplication. The cytotoxicity of saikosaponin d against HepG2 human hepatocellular carcinoma cells was due to the induction of apoptosis through the activation of caspases 3 and 7, which subsequently resulted in poly-ADP-ribose-polymerase (PARP) cleavage. DNA fragmentation was clearly noted at more than 6 h after HepG2 cells exposure to saikosaponin d. The present study concludes that saikosaponin c exhibits anti-HBV activity and saikosaponin d possesses potent cytotoxicity against human hepatocellular carcinoma cells.
引用
收藏
页码:705 / 709
页数:5
相关论文
共 21 条
[1]  
Ayoola E. A., 1988, Bull. World Health Org, V66, P443
[2]  
BEASLEY RP, 1983, LANCET, V2, P1099
[3]   INCIDENCE OF HEPATITIS-B VIRUS-INFECTIONS IN PRESCHOOL-CHILDREN IN TAIWAN [J].
BEASLEY, RP ;
HWANG, LY ;
LIN, CC ;
LEU, ML ;
STEVENS, CE ;
SZMUNESS, W ;
CHEN, KP .
JOURNAL OF INFECTIOUS DISEASES, 1982, 146 (02) :198-204
[4]  
BEASLEY RP, 1981, LANCET, V2, P1129
[5]   Hepatitis B vaccination and hepatocellular carcinoma rates in boys and girls [J].
Chang, MH ;
Shau, WY ;
Chen, CJ ;
Wu, TC ;
Kong, MS ;
Liang, DC ;
Hsu, HM ;
Chen, HL ;
Hsu, HY ;
Chen, DS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 284 (23) :3040-3042
[6]  
CHANG RS, 1988, ANTIVIR RES, V9, P163, DOI 10.1016/0166-3542(88)90001-0
[7]  
DAVID L, 1998, LEINWAND CELL LAB MA, P1511
[8]   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
[9]   LONG-TERM FOLLOW-UP OF ANTI-HBE-POSITIVE CHRONIC ACTIVE HEPATITIS-B [J].
FATTOVICH, G ;
BROLLO, L ;
ALBERTI, A ;
PONTISSO, P ;
GIUSTINA, G ;
REALDI, G .
HEPATOLOGY, 1988, 8 (06) :1651-1654
[10]  
GATO W, 1996, PHYTOTHER RES, V10, P504