OECD test strategies and methods for endocrine disruptors

被引:50
作者
Gelbke, HP
Kayser, M
Poole, A
机构
[1] GUP, Dept Prod Safety, D-67056 Ludwigshafen, Germany
[2] DOW Europe SA, CH-8810 Horgen, Switzerland
关键词
endocrine disruptors; validation of OECD test methods; uterotrophic assay; Hershberger assay; enhancedsubacute test (OECD TG 407);
D O I
10.1016/j.tox.2004.06.034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The question whether (man-made or natural) chemical substances may have an adverse effect on the endocrine system has gained high visibility in the public as well as in the scientific community. This relates to possible effects on the environment as well as on human health for chemicals with (anti)estrogenic, (anti)androgenic or (anti)thyroid activity. Taking into account the broad universe of chemicals to which humans or the environment may be exposed, a sound testing strategy and robust test methods are urgently needed. Both subjects have been addressed by a specific OECD working group (EDTA - Endocrine Disruptor Testing and Assessment Task Force) involving regulatory agencies, the scientific community, chemical industry and NGOs. Like other organizations the OECD has adopted a tiered-testing strategy with the first tier using screening assays as quick and inexpensive tools, providing a way of generating alerts to potential endocrine activity that can be used to prioritize substances for definitive tests that then can determine the toxicological consequences of endocrine toxicity. The efforts of the OECD have therefore concentrated on the validation of specific screening and testing guidelines, like the uterotrophic, the Hershberger, and the "enhanced TG 407" test. The experimental testing necessary for this validation procedure is completed for the uterotrophic and the "enhanced TG 407" tests and near completion for the Hershberger assay. The data obtained so far have been published (for the uterotrophic assay) or will be submitted to the EDTA working group for final evaluation. Overall, the validation program has been very successful and should be sufficient for setting up OECD test guidelines for these experimental procedures. This will add substantially to the "tool-box" of OECD test methods that is available internationally to regulatory agencies and chemical industry for the identification and assessment of possible endocrine disruptors. Despite this success it is well recognized that the methodological "tool-box" should be supplemented by further screening and testing procedures related to effects on human health and the environment. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:17 / 25
页数:9
相关论文
共 35 条
[1]   Effects of 17β-estradiol on serum hormone concentrations and estrous cycle in female Crl:CD BR rats:: Effects on parental and first generation rats [J].
Biegel, LB ;
Cook, JC ;
Hurtt, ME ;
O'Connor, JC .
TOXICOLOGICAL SCIENCES, 1998, 44 (02) :143-154
[2]   90-day feeding and one-generation reproduction study in Crl:CD BR rats with 17β-estradiol [J].
Biegel, LB ;
Flaws, JA ;
Hirshfield, AN ;
O'Connor, JC ;
Elliott, GS ;
Ladics, GS ;
Silbergeld, EK ;
Van Pelt, CS ;
Hurtt, ME ;
Cook, JC ;
Frame, SR .
TOXICOLOGICAL SCIENCES, 1998, 44 (02) :116-142
[3]   The effects of 4-nonylphenol in rats: A multigeneration reproduction study [J].
Chapin, RE ;
Delaney, J ;
Wang, YF ;
Lanning, L ;
Davis, B ;
Collins, B ;
Mintz, N ;
Wolfe, G .
TOXICOLOGICAL SCIENCES, 1999, 52 (01) :80-91
[4]   Effects of dietary 17β-estradiol exposure on serum hormone concentrations and testicular parameters in male Crl:CD BR rats [J].
Cook, JC ;
Johnson, L ;
O'Connor, JC ;
Biegel, LB ;
Krams, CH ;
Frame, SR ;
Hurtt, ME .
TOXICOLOGICAL SCIENCES, 1998, 44 (02) :155-168
[5]  
*CSTEE, 1999, OP HUM WILDL HLTH EF
[6]   Subchronic toxicity (90-day) study with para-nonylphenol in rats [J].
Cunny, HC ;
Mayes, BA ;
Rosica, KA ;
Trutter, JA ;
VanMiller, JP .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1997, 26 (02) :172-178
[7]   I. The effect of p-nonylphenol, an environmental toxicant with oestrogenic properties, on fertility potential in adult male rats [J].
de Jager, C ;
Bornman, MS ;
van der Horst, G .
ANDROLOGIA, 1999, 31 (02) :99-106
[8]   II. The effect of p-nonylphenol on the fertility potential of male rats after gestational, lactational and direct exposure [J].
de Jager, C ;
Bornman, MS ;
Oosthuizen, JMC .
ANDROLOGIA, 1999, 31 (02) :107-113
[9]  
DECLOS KB, 2003, TOXICOL SCI, V72, P76
[10]   Effects of dietary genistein exposure during development on male and female CD (Sprague-Dawley) rats [J].
Delclos, KB ;
Bucci, TJ ;
Lomax, LG ;
Latendresse, JR ;
Warbritton, A ;
Weis, CC ;
Newbold, RR .
REPRODUCTIVE TOXICOLOGY, 2001, 15 (06) :647-663