Chemical and biological analysis of active free and conjugated bile acids in animal bile using HPLC-ELSD and MTT methods

被引:9
作者
Wang, Ning [1 ]
Feng, Yibin [1 ]
Xie, Tang Ning [4 ]
Su, Weiwei [4 ]
Zhu, Meifen [1 ]
Chow, Oiyee [1 ]
Zhang, Yanbo [1 ]
Ng, Kwan-Ming [2 ,3 ]
Leung, Chung-Hang [2 ,3 ]
Tong, Yao [1 ]
机构
[1] Univ Hong Kong, Sch Chinese Med, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Fac Sci, Dept Chem, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Fac Sci, Open Lab Chem Biol, Inst Mol Technol Drug Discovery & Synth, Hong Kong, Hong Kong, Peoples R China
[4] Sun Yat Sen Univ, Sch Life Sci, Guangzhou 510275, Guangdong, Peoples R China
关键词
animal bile; bile acids; high performance liquid chromatography-evaporative light scattering detector system; cytotoxicity; hepatocellular carcinoma; INDUCE APOPTOSIS; MODULATION; GROWTH;
D O I
10.3892/etm.2010.178
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The aim of the present study was to determine the chemical composition and in vitro cytotoxic activity of seven bile samples and bile acids using the high-performance liquid chromatography (HPLC)-evaporative light scattering detector (ELSD) method. Free and conjugated bile acid standards were used to identify and quantify the chemical components of the seven animal bile samples. The MTT assay was used to determine the cytotoxic effect of the animal bile samples and the free and conjugated bile acids on hepatocellular carcinoma MHCC97-L cells. Chemical analysis revealed that the bile samples from the different animals shared little similarity in terms of their composition. A cell viability assay revealed that cattle bile, as well as its major components, DCA, CDCA and TCDCA, exhibited a marked cytotoxic effect on the hepatocellular carcinoma MHCC97-L cells. The bear bile samples that originated from the Asian black bear and the American black bear contained a unique component, TUDCA, which distinguished them from the other animal bile, though their inhibitory action on MHCC97-L cells was not markedly distinct. The present study reveals that cattle bile may be a potential alternative to bear bile for hepatocarcinoma therapy.
引用
收藏
页码:125 / 130
页数:6
相关论文
共 15 条
  • [1] Bear bile: dilemma of traditional medicinal use and animal protection
    Feng, Yibin
    Siu, Kayu
    Wang, Ning
    Ng, Kwan-Ming
    Tsao, Sai-Wah
    Nagamatsu, Tadashi
    Tong, Yao
    [J]. JOURNAL OF ETHNOBIOLOGY AND ETHNOMEDICINE, 2009, 5
  • [2] Apoptosis and Modulation of Cell Cycle Control by Bile Acids in Human Leukemia T Cells
    Fimognari, Carmela
    Lenzi, Monia
    Cantelli-Forti, Giorgio
    Hrellia, Patrizia
    [J]. NATURAL COMPOUNDS AND THEIR ROLE IN APOPTOTIC CELL SIGNALING PATHWAYS, 2009, 1171 : 264 - 269
  • [3] Gu Xianchen, 1994, Zhongguo Zhongyao Zazhi, V19, P556
  • [4] KINAMI Y, 1993, ONCOLOGY, V50, P46
  • [5] ETHNOPHARMACOLOGY OF BEAR GALL-BLADDER .1.
    LI, YW
    ZHU, XY
    BUT, PPH
    YEUNG, HW
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 1995, 47 (01) : 27 - 31
  • [6] Ursodeoxycholic acid switches oxaliplatin-induced necrosis to apoptosis by inhibiting reactive oxygen species production and activating p53-caspase 8 pathway in HepG2 hepatocellular carcinoma
    Lim, Sung-Chul
    Choi, Jeong Eun
    Kang, Ho Sung
    Si, Han
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2010, 126 (07) : 1582 - 1595
  • [7] Park SE, 2004, INT J ONCOL, V25, P231
  • [8] Tauroursodeoxycholic acid reduces bile acid-induced apoptosis by modulation of AP-1
    Pusl, Thomas
    Vennegeerts, Timo
    Wimmer, Ralf
    Denk, Gerald U.
    Beuers, Ulrich
    Rust, Christian
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 367 (01) : 208 - 212
  • [9] Administration of tauroursodeoxycholic acid (TUDCA) reduces apoptosis following myocardial infarction in rat
    Rivard, Andrew L.
    Steer, Clifford J.
    Kren, Betsy T.
    Rodrigues, Cecilia M. P.
    Castro, Rui E.
    Bianco, Richard W.
    Low, Walter C.
    [J]. AMERICAN JOURNAL OF CHINESE MEDICINE, 2007, 35 (02): : 279 - 295
  • [10] Sola S.CastroRE, 2006, BIOCHEMISTRY-US, V43, P8429