Lycopene oxidation product enhances gap junctional communication

被引:118
作者
Aust, O
Ale-Agha, N
Zhang, L
Wollersen, H
Sies, H
Stahl, W
机构
[1] Univ Dusseldorf, Inst Biochem & Mol Biol 1, D-40001 Dusseldorf, Germany
[2] Univ Gesamthsch Paderborn, Fachbereich Chem & Chem Tech 13, D-33098 Paderborn, Germany
关键词
carotenoids; lycopene oxidation product; gap junctional communication;
D O I
10.1016/S0278-6915(03)00148-0
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Carotenoids as well as their metabolites and oxidation products stimulate gap junctional communication (GJC) between cells, which is thought to be one of the protective mechanisms related to cancer-preventive activities of these compounds. Increased intake of lycopene by consumption of tomatoes or tomato products has been epidemiologically associated with a diminished risk of prostate cancer. Here, we report a stimulatory effect of a lycopene oxidation product on GJC in rat liver epithelial WB-F344 cells. The active compound was obtained by complete in vitro oxidation of lycopene with hydrogen peroxide/osmium tetroxide. For structural analysis high performance liquid chromatography, gas chromatography coupled with mass spectrometry, ultraviolet/visible-, and infrared spectrophotometry were applied. The biologically active oxidation product was identified as 2,7,1 1-trimethyltetradecahexaene-1, 14-dial. The present data indicate a potential role of lycopene degradation products in cell signaling enhancing cell-to-cell communication via gap junctions. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1399 / 1407
页数:9
相关论文
共 32 条
  • [1] (-)-Epicatechin effects in rat liver epithelial cells:: stimulation of gap junctional communication and counteraction of its loss due to the tumor promoter 12-O-tetradecanoylphorbol-13-acetate
    Ale-Agha, N
    Stahl, W
    Sies, H
    [J]. BIOCHEMICAL PHARMACOLOGY, 2002, 63 (12) : 2145 - 2149
  • [2] Bast A, 1998, INT J VITAM NUTR RES, V68, P399
  • [3] Berridge M.V., 1996, Biochemica, P14, DOI DOI 10.1155/2013/420601
  • [4] DIVERSE CAROTENOIDS PROTECT AGAINST CHEMICALLY-INDUCED NEOPLASTIC TRANSFORMATION
    BERTRAM, JS
    PUNG, A
    CHURLEY, M
    KAPPOCK, TJ
    WILKINS, LR
    COONEY, RV
    [J]. CARCINOGENESIS, 1991, 12 (04) : 671 - 678
  • [5] Bertram JS, 1999, NUTR REV, V57, P182, DOI 10.1111/j.1753-4887.1999.tb06941.x
  • [6] BERTRAM JS, 2000, ANTIOXIDANT REDOX RE, P409
  • [7] BRITTON G, 1995, CAROTENOIDS B, V1, P46
  • [8] Britton G., 1995, CAROTENOIDS B, V1B, P20
  • [9] Donaldson P, 1997, HISTOL HISTOPATHOL, V12, P219
  • [10] Gap junctions: structure and function (Review)
    Evans, WH
    Martin, PEM
    [J]. MOLECULAR MEMBRANE BIOLOGY, 2002, 19 (02) : 121 - 136