Metabolism of isoflavones and lignans by the gut microflora: a study in germ-free and human flora associated rats

被引:279
作者
Bowey, E
Adlercreutz, H
Rowland, I [1 ]
机构
[1] Univ Ulster, No Ireland Ctr Food & Hlth, Coleraine BT52 1SA, Londonderry, North Ireland
[2] BIBRA Int Ltd, Carshalton SM5 4DS, Surrey, England
[3] Univ Helsinki, Inst Prevent Med Nutr & Canc, Folkhalsan Res Ctr, FIN-00014 Helsinki, Finland
[4] Univ Helsinki, Div Clin Chem, FIN-00014 Helsinki, Finland
关键词
phytoestrogens; daidzein; genistein; equol; gut bacteria;
D O I
10.1016/S0278-6915(02)00324-1
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
We have investigated the metabolism of isoflavones and lignans in germ-free (GF) rats and rats associated with human faecal bacteria (human flora associated [HFA] rats), in order to provide unequivocal evidence for the role of the gut microflora in the absorption and metabolism of these phytoestrogens. Furthermore, we have investigated whether certain metabolic characteristics (high equol-producing and low equol-producing status) of human intestinal floras can be transferred to GF rats. Germ-free rats fed a soy-isoflavone containing diet excreted large quantities of daidzein and genistein in urine indicating that the gut microflora is not required for the absorption of isoflavones. The isoflavone metabolites equol, O-desmethylangolensin and the lignan enterolactone were not detectable in urine from the GF rats, but were present in HFA rat urine, indicating that they were products of gut microflora activity. Colonization of GF rats with a faecal flora from a human subject with the capacity to convert daidzein to equol, resulted in the rats excreting substantial amounts of the metabolite. In contrast, equol was undetectable in urine of HFA rats associated with a faecal flora from a low equol-producing subject. The results therefore show that the inability of some subjects to produce equol is a consequence of the lack of specific components of the gut microflora. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:631 / 636
页数:6
相关论文
共 39 条
  • [1] DETERMINATION OF URINARY LIGNANS AND PHYTOESTROGEN METABOLITES, POTENTIAL ANTIESTROGENS AND ANTICARCINOGENS, IN URINE OF WOMEN ON VARIOUS HABITUAL DIETS
    ADLERCREUTZ, H
    FOTSIS, T
    BANNWART, C
    WAHALA, K
    MAKELA, T
    BRUNOW, G
    HASE, T
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1986, 25 (5B) : 791 - 797
  • [2] ISOTOPE-DILUTION GAS-CHROMATOGRAPHIC MASS-SPECTROMETRIC METHOD FOR THE DETERMINATION OF LIGNANS AND ISOFLAVONOIDS IN HUMAN URINE, INCLUDING IDENTIFICATION OF GENISTEIN
    ADLERCREUTZ, H
    FOTSIS, T
    BANNWART, C
    WAHALA, K
    BRUNOW, G
    HASE, T
    [J]. CLINICA CHIMICA ACTA, 1991, 199 (03) : 263 - 278
  • [3] Phyto-oestrogens and Western diseases
    Adlercreutz, H
    Mazur, W
    [J]. ANNALS OF MEDICINE, 1997, 29 (02) : 95 - 120
  • [4] Absorption and metabolism of genistin in the isolated rat small intestine
    Andlauer, W
    Kolb, J
    Fürst, P
    [J]. FEBS LETTERS, 2000, 475 (02) : 127 - 130
  • [5] THE IDENTIFICATION OF THE WEAK ESTROGEN EQUOL [7-HYDROXY-3-(4'-HYDROXYPHENYL)CHROMAN] IN HUMAN-URINE
    AXELSON, M
    KIRK, DN
    FARRANT, RD
    COOLEY, G
    LAWSON, AM
    SETCHELL, KDR
    [J]. BIOCHEMICAL JOURNAL, 1982, 201 (02) : 353 - 357
  • [6] SOYA - A DIETARY SOURCE OF THE NON-STEROIDAL ESTROGEN EQUOL IN MAN AND ANIMALS
    AXELSON, M
    SJOVALL, J
    GUSTAFSSON, BE
    SETCHELL, KDR
    [J]. JOURNAL OF ENDOCRINOLOGY, 1984, 102 (01) : 49 - 56
  • [7] Phyto-oestrogens: Where are we now?
    Bingham, SA
    Atkinson, C
    Liggins, J
    Bluck, L
    Coward, A
    [J]. BRITISH JOURNAL OF NUTRITION, 1998, 79 (05) : 393 - 406
  • [8] PRODUCTION AND METABOLISM OF LIGNANS BY THE HUMAN FECAL FLORA
    BORRIELLO, SP
    SETCHELL, KDR
    AXELSON, M
    LAWSON, AM
    [J]. JOURNAL OF APPLIED BACTERIOLOGY, 1985, 58 (01): : 37 - 43
  • [9] Pharmacokinetics of [14C]Genistein in the rat:: Gender-related differences, potential mechanisms of biological action, and implications for human health
    Coldham, NG
    Sauer, MJ
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2000, 164 (02) : 206 - 215
  • [10] Biotransformation of genistein in the rat: elucidation of metabolite structure by product ion mass fragmentology
    Coldham, NG
    Howells, LC
    Santi, A
    Montesissa, C
    Langlais, C
    King, LJ
    Macpherson, DD
    Sauer, MJ
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1999, 70 (4-6) : 169 - 184