Gender differences in the levels of bisphenol A metabolites in urine

被引:117
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 [J].
Kadoma, Y ;
Fujisawa, S .
BIOMATERIALS, 2000, 21 (21) :2125-2130
[5]   METABOLISM OF BISPHENOL A IN RAT [J].
KNAAK, JB ;
SULLIVAN, LJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1966, 8 (02) :175-&
[6]   Bisphenol A levels in human urine [J].
Matsumoto, A ;
Kunugita, N ;
Kitagawa, K ;
Isse, T ;
Oyama, T ;
Foureman, GL ;
Morita, M ;
Kawamoto, T .
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 [J].
Mori, C ;
Komiyama, M ;
Adachi, T ;
Sakurai, K ;
Nishimura, D ;
Takashima, K ;
Todaka, E .
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 [J].
Perera, FP ;
Illman, SM ;
Kinney, PL ;
Whyatt, RM ;
Kelvin, EA ;
Shepard, P ;
Evans, D ;
Fullilove, M ;
Ford, J ;
Miller, RL ;
Mayer, IH ;
Rauh, VA .
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 [J].
Pottenger, LH ;
Domoradzki, JY ;
Markham, DA ;
Hansen, SC ;
Cagen, SZ ;
Waechter, JM .
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 [J].
Roy, D ;
Palangat, M ;
Chen, CW ;
Thomas, RD ;
Colerangle, J ;
Atkinson, A ;
Yan, ZJ .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1997, 50 (01) :1-29