Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (50)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Le Guevel, R.
Right arrow Articles by Pakdel, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Le Guevel, R.
Right arrow Articles by Pakdel, F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 16, No. 5, 1030-1036, May 2001
© 2001 European Society of Human Reproduction and Embryology

Assessment of oestrogenic potency of chemicals used as growth promoter by in-vitro methods

Rémy Le Guevel1, and Farzad Pakdel

Équipe d'Endocrinologie Moléculaire de la Reproduction, UMR CNRS 6026 Université de Rennes I, Campus de Beaulieu, France

Three in-vitro bioassays were used to compare the oestrogenic potency of chemicals used as growth promoter in beef cattle in certain non-European Union countries (17ß-oestradiol, {alpha}-zearalanol, testosterone, trenbolone, trenbolone acetate, melengestrol acetate) or found as food contaminant such as the mycotoxin zearalenone and some of their metabolites (17{alpha}-oestradiol, oestrone, 17{alpha}-epitestosterone, 19-nortestosterone, androstendione, zearalanone, {alpha}-zearalanol, ß-zearalanol, {alpha}-zearalenol, ß-zearalenol). The strong oestrogens 17{alpha}-ethinyl oestradiol and diethylstilboestrol were used as standards. The first bioassay was based on the activation of a reporter gene by oestrogens in recombinant yeast expressing human or rainbow trout oestrogen receptor. In the second bioassay, the vitellogenin gene induction of rainbow trout hepatocyte cultures was used as a biomarker for the exposure to oestrogens. The third bioassay was based on the alkaline phosphatase gene induction by oestrogens in the human endometrial Ishikawa cell line. The assessment of oestrogenic potency of these chemicals clearly demonstrates the strong oestrogenicity of the mycotoxin zearalenone and its metabolites and particularly {alpha}-zearalenol which was as potent as ethinyl oestradiol and diethylstilboestrol in the human endometrial Ishikawa cell line.

Key words: growth promoters/in-vitro assays/meat hormones/oestrogen/oestrogenic potency

1 To whom correspondence should be addressed at: Équipe d'Endocrinologie Moléculaire de la Reproduction, UMR CNRS 6026, Université de Rennes I, Campus de Beaulieu, 35042 Rennes cedex, France. E-mail: Remy.Le-Guevel{at}univ-rennes1.fr


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Exp Biol MedHome page
S. L. Gray, B. R. Lackey, P. L. Tate, M. B. Riley, and N. D. Camper
Mycotoxins in Root Extracts of American and Asian Ginseng Bind Estrogen Receptors {alpha} and {beta}
Exp Biol Med, June 1, 2004; 229(6): 560 - 568.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
R. E. Nelson, S. K. Grebe, D. J. O'Kane, and R. J. Singh
Liquid Chromatography-Tandem Mass Spectrometry Assay for Simultaneous Measurement of Estradiol and Estrone in Human Plasma
Clin. Chem., February 1, 2004; 50(2): 373 - 384.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.