Gender differences in the levels of bisphenol A metabolites in urine

被引:115
作者
Kim, YH
Kim, CS
Park, S
Han, SY
Pyo, MY
Yang, MH
机构
[1] Seoul Natl Univ, Sch Med, Dept Prevent Med, Seoul 110799, South Korea
[2] Korea Food & Drug Adm, Natl Inst Toxicol Res, Endocrine Toxicol Div, Seoul 122704, South Korea
[3] Soomyung Womens Univ, Dept Pharm, Seoul 140742, South Korea
[4] Seoul Natl Univ, Sch Med, Canc Res Inst, Seoul 110799, South Korea
关键词
bisphenol A; endocrine disruptor; beta-glueuronidase; sulfatase; urinary conjugates;
D O I
10.1016/j.bbrc.2003.10.135
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The metabolism of bisphenol A (BPA), a suspected endocrine disruptor, should be considered for monitoring human exposure to BPA, because the conjugation with beta-D-glucuronide and sulfate reduces the estrogenic activity. In this study, BPA levels in 30 healthy Koreans (men, N = 15, 42.6 +/- 2.4 years; women, N = 15, 43.0 +/- 2.7 years) were analyzed from urine treated with/without beta-glucuronidase and/or sulfatase by an RP-HPLC with fluorescence detection. The total BPA concentrations including free BPA and the urinary conjugates were similar in men and women (2.82 +/- 0.73 and 2.76 +/- 0.54 ng ml(-1), respectively), but gender differences were found in the levels of urinary BPA conjugates. Men had significantly higher levels of BPA-glucuronide (2.34 +/- 0.85 ng ml-1) than women (1.00 +/- 0.34 ng ml(-1)), whereas women had higher levels of BPA-sulfate (1.20 +/- 0.32 ng ml(-1)) than men (0.49 +/- 0.27 ng ml(-1)). (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:441 / 448
页数:8
相关论文
共 20 条
  • [1] Andersson A. M., 2001, HORMONES ENDOCRINE D
  • [2] Colborn T., 1996, OUR STOLEN FUTURE
  • [3] Elsby R, 2001, J PHARMACOL EXP THER, V297, P103
  • [4] Kinetic evaluation of reactivity of bisphenol A derivatives as radical scavengers for methacrylate polymerization
    Kadoma, Y
    Fujisawa, S
    [J]. BIOMATERIALS, 2000, 21 (21) : 2125 - 2130
  • [5] METABOLISM OF BISPHENOL A IN RAT
    KNAAK, JB
    SULLIVAN, LJ
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1966, 8 (02) : 175 - &
  • [6] Bisphenol A levels in human urine
    Matsumoto, A
    Kunugita, N
    Kitagawa, K
    Isse, T
    Oyama, T
    Foureman, GL
    Morita, M
    Kawamoto, T
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (01) : 101 - 104
  • [7] Application of toxicogenomic analysis to risk assessment of delayed long-term effects of multiple chemicals, including endocrine disruptors in human fetuses
    Mori, C
    Komiyama, M
    Adachi, T
    Sakurai, K
    Nishimura, D
    Takashima, K
    Todaka, E
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (06) : 803 - 809
  • [8] The challenge of preventing environmentally related disease in young children: Community-based research in New York City
    Perera, FP
    Illman, SM
    Kinney, PL
    Whyatt, RM
    Kelvin, EA
    Shepard, P
    Evans, D
    Fullilove, M
    Ford, J
    Miller, RL
    Mayer, IH
    Rauh, VA
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 2002, 110 (02) : 197 - 204
  • [9] The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration
    Pottenger, LH
    Domoradzki, JY
    Markham, DA
    Hansen, SC
    Cagen, SZ
    Waechter, JM
    [J]. TOXICOLOGICAL SCIENCES, 2000, 54 (01) : 3 - 18
  • [10] Biochemical and molecular changes at the cellular level in response to exposure to environmental estrogen-like chemicals
    Roy, D
    Palangat, M
    Chen, CW
    Thomas, RD
    Colerangle, J
    Atkinson, A
    Yan, ZJ
    [J]. JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1997, 50 (01): : 1 - 29