Metabolism of the olive oil phenols hydroxytyrosol, tyrosol, and hydroxytyrosyl acetate by human hepatoma HepG2 cells

被引:70
|
作者
Mateos, R [1 ]
Goya, L [1 ]
Bravo, L [1 ]
机构
[1] CSIC, Inst Frio, Dept Metab & Nutr, E-28040 Madrid, Spain
关键词
phenols; virgin olive oil; metabolism; in vitro conjugation; HepG2; cells; LC-MS analysis;
D O I
10.1021/jf051721q
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
To study the potential hepatic metabolism of olive oil phenols, human hepatoma HepG2 cells were incubated for 2 and 18 h with hydroxytyrosol, tyrosol, and hydroxytyrosyl acetate, three phenolic constituents of olive oil. After incubation, culture media and cell lysates were hydrolyzed with beta-glucuronidase and sulfatase and analyzed by LC-MS. In vitro methylation, glucuronidation, and sulfation of pure phenols were also performed. Methylated and glucuronidated forms of hydroxytyrosol were detected at 18 h of incubation, together with methylglucuronidated metabolites. Hydroxytyrosyl acetate was largely converted into free hydroxytyrosol and subsequently metabolized, yet small amounts of glucuronidated hydroxytyrosyl acetate were detected. Tyrosol was poorly metabolized, with < 10% of the phenol glucuronidated after 18 h. Minor amounts of free or conjugated phenols were detected in cell lysates. No sulfated metabolites were found. In conclusion, olive oil phenols can be metabolized by the liver as suggested by the results obtained using HepG2 cells as a hepatic model system.
引用
收藏
页码:9897 / 9905
页数:9
相关论文
共 50 条
  • [41] Octreotide induces caspase activation and apoptosis in human hepatoma HepG2 cells
    Nikos J Tsagarakis
    Ioannis Drygiannakis
    Antonis G Batistakis
    George Kolios
    Elias A Kouroumalis
    World Journal of Gastroenterology, 2011, 17 (03) : 313 - 321
  • [42] Cytotoxicity and Apoptosis Induction in Human HepG2 Hepatoma Cells by Decabromodiphenyl Ethane
    SUN Ru Bao 1
    2.Beijing Institute of Disease Control and Prevention
    BiomedicalandEnvironmentalSciences, 2012, 25 (05) : 495 - 501
  • [43] Inhibition of apolipoprotein B and triglyceride secretion in human hepatoma cells (HepG2)
    Haghpassand, M
    Wilder, D
    Moberly, JB
    JOURNAL OF LIPID RESEARCH, 1996, 37 (07) : 1468 - 1480
  • [44] Effect of lanthanum citrate on anoikis resistance in human hepatoma cells HepG2
    Su, Xiang-E
    Zheng, Xiao-Na
    Shenzhen Daxue Xuebao (Ligong Ban)/Journal of Shenzhen University Science and Engineering, 2010, 27 (02): : 236 - 240
  • [45] The toxicity of troglitazone, rosiglitazone and vitamin E in HepG2 human hepatoma cells
    Ball, AJ
    Tettey, JNA
    Grant, MH
    TOXICOLOGY, 2004, 194 (03) : 250 - 251
  • [46] Enhancement of Doxorubicin Cytotoxicity by Tanshinone IIA in HepG2 Human Hepatoma Cells
    Kan, Shidong
    Cheung, Wan Man
    Zhou, Yanling
    Ho, Wing Shing
    PLANTA MEDICA, 2014, 80 (01) : 70 - 76
  • [47] Cytotoxicity and Apoptosis Induction in Human HepG2 Hepatoma Cells by Decabromodiphenyl Ethane
    Sun Ru Bao
    Xi Zhu Ge
    Yan Jun
    Yang Hong Lian
    BIOMEDICAL AND ENVIRONMENTAL SCIENCES, 2012, 25 (05) : 495 - 501
  • [48] Histidine and protein metabolism in human liver cells (HepG2).
    Shaw, HA
    Failla, ML
    Cave, KD
    Hopkins, R
    Park, K
    FASEB JOURNAL, 1997, 11 (03): : 2125 - 2125
  • [49] REGULATION OF APOLIPOPROTEIN SECRETION BY HUMAN HEPATOMA, HEPG2
    CRAIG, WY
    COOPER, AD
    ARTERIOSCLEROSIS, 1986, 6 (05): : A536 - A537
  • [50] Induction of apoptosis and inhibition of growth of human hepatoma HepG2 cells by heparin
    Karti, SS
    Ovali, E
    Ozgur, O
    Yilmaz, M
    Sonmez, M
    Ratip, S
    Ozdemir, F
    HEPATO-GASTROENTEROLOGY, 2003, 50 (54) : 1864 - 1866