Assessment of deoxynivalenol metabolite profiles in UK adults

被引:73
作者
Turner, Paul C. [1 ,2 ]
Hopton, Richard P. [1 ,2 ,3 ]
White, Kay L. M. [1 ,2 ]
Fisher, Julie [3 ]
Cade, Janet E. [1 ,2 ]
Wild, Christopher P. [4 ]
机构
[1] Univ Leeds, Ctr Biostat & Epidemiol, Mol Epidemiol Unit, Leeds Inst Genet Hlth & Therapeut, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Ctr Biostat & Epidemiol, Nutr Epidemiol Grp, Leeds Inst Genet Hlth & Therapeut, Leeds LS2 9JT, W Yorkshire, England
[3] Univ Leeds, Sch Chem, Leeds LS2 9JT, W Yorkshire, England
[4] IARC, F-69372 Lyon 08, France
关键词
Biomarker; Deoxynivalenol; Diet; Metabolism; Urine; UK; URINARY DEOXYNIVALENOL; TOXICOLOGY; WHEAT; TRICHOTHECENES; CONSUMPTION; EXCRETION; LEVEL; FECES;
D O I
10.1016/j.fct.2010.10.007
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Deoxynivalenol (DON) requires no activation for toxicity, though susceptibility may reflect individual variations in detoxification. This study reports the measurement of un-metabolised urinary DON (free DON) and DOM-1 in samples previously analysed for the combined measure of free DON + DON-glucuronide (fD + DG), with a concentration > 5 ng/ml, for 34 UK adults. Four consecutive daily urine samples were analysed from twenty-two individuals, whilst from 12 individuals only a single sample was analysed. The mean (median) concentration of urinary fD + DG in this sub-set was 17.8 ng/ml (13.8 ng/ml), range 5.0-78.2 ng/ml. In 23/34 (68%) individuals, free DON was detected, mean 2.4 ng/ml; range 0.5-9.3 ng/ml. Urinary DOM-1 was detected in 1/34(3%) of individuals; present at similar to 1% of urinary fD + DG concentration for that individual. The concentration of fD + DG combined was significantly correlated with urinary free DON (p < 0.001, R-2 = 0.65), but not with the percentage of free DON to fD + DG (p = 0.615, R-2 = 0.01), suggesting that the level of DON exposure did not affect the metabolism to DG within the range observed. In this survey most individuals had no detectable urinary DOM-1 and 68% did not detoxify all of the ingested DON to DON-glucuronide. This study needs to be extended to understand whether the fD / DG ratio provides a phenotypic measure of DON susceptibility. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:132 / 135
页数:4
相关论文
共 26 条
  • [1] Suppression of Insulin-Like Growth Factor Acid-Labile Subunit Expression-A Novel Mechanism for Deoxynivalenol-Induced Growth Retardation
    Amuzie, Chidozie J.
    Pestka, James J.
    [J]. TOXICOLOGICAL SCIENCES, 2010, 113 (02) : 412 - 421
  • [2] BHAT RV, 1989, LANCET, V1, P35
  • [3] EXCRETION OF DEOXYNIVALENOL AND ITS METABOLITE IN MILK, URINE, AND FECES OF LACTATING DAIRY-COWS
    COTE, LM
    DAHLEM, AM
    YOSHIZAWA, T
    SWANSON, SP
    BUCK, WB
    [J]. JOURNAL OF DAIRY SCIENCE, 1986, 69 (09) : 2416 - 2423
  • [4] Comparative cytotoxicity of deoxynivalenol, nivalenol, their acetylated derivatives and de-epoxy metabolites
    Eriksen, GS
    Pettersson, H
    Lundh, T
    [J]. FOOD AND CHEMICAL TOXICOLOGY, 2004, 42 (04) : 619 - 624
  • [5] Lack of de-epoxidation of type B trichothecenes in incubates with human faeces
    Eriksen, GS
    Pettersson, H
    [J]. FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 2003, 20 (06): : 579 - 582
  • [6] Transformation of trichothecenes in ileal digesta and faeces from pigs
    Eriksen, GS
    Pettersson, H
    Johnsen, K
    Lindberg, JE
    [J]. ARCHIVES OF ANIMAL NUTRITION, 2002, 56 (04) : 263 - 274
  • [7] Bioavailability of the Fusarium toxin deoxynivalenol (DON) from naturally contaminated wheat for the pig
    Goyarts, T
    Dänicke, S
    [J]. TOXICOLOGY LETTERS, 2006, 163 (03) : 171 - 182
  • [8] GROOPMAN ID, 1993, ENV HLTH PERSPECT, V99, P107
  • [9] IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2002, IARC Monogr Eval Carcinog Risks Hum, V82, P1
  • [10] Luo X., 1994, PROCEDURES 2 ASIAN C, P129