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 (52)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Thayer, K.A.
Right arrow Articles by vom Saal, F.S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Thayer, K.A.
Right arrow Articles by vom Saal, F.S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 16, No. 5, 988-996, May 2001
© 2001 European Society of Human Reproduction and Embryology

Altered prostate growth and daily sperm production in male mice exposed prenatally to subclinical doses of 17{alpha}-ethinyl oestradiol

K.A. Thayer1,5, R.L. Ruhlen2, K.L. Howdeshell1, D.L. Buchanan3, P.S. Cooke3, D. Preziosi2, W.V. Welshons2, J. Haseman4 and F.S. vom Saal1

1 Department of Biological Sciences, University of Missouri-Columbia, Columbia, Missouri, 2 Department of Veterinary Biomedical Sciences, University of Missouri-Columbia, Columbia, Missouri, 3 Department of Veterinary Biosciences, University of Illinois at Urbana-Champaign, Urbana, Illinois and 4 National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA

Approximately 2 million women in the USA and Europe continue taking oral contraceptives each year during undetected pregnancy due primarily to non-compliance and also to individual variation in sensitivity to hormones in the contraceptives. Prenatal exposure to oral contraceptives containing 17{alpha}-ethinyl oestradiol (EE) has generally not been associated with an increased incidence of externally observable malformations at birth. The purpose of this study was to assess effects on reproductive organs in adult male mice that had been exposed during gestation day 0 through 17 (equivalent to gestation week 16 in humans) to clinically relevant (~0.5 µg/kg/day) and lower doses of EE. Doses used in this study ranged from 0.002 to 2 µg/kg/day. By 5 months of age, prostate weight was significantly (P < 0.05) higher than controls in most treatment groups of EE (0.02–2 µg/kg). Prostatic androgen receptor populations were significantly elevated only in the 0.02 µg/kg group, suggesting different mechanisms for the increase in prostate weight at different doses. Daily sperm production (DSP) and DSP per gramme of testis were reduced in all treatment groups during adolescence, but not later in adulthood. These findings are consistent with prior studies showing that prenatal exposure of mice to very low doses of a number of oestrogenic chemicals can alter the adult male reproductive system without causing gross external malformations.

Key words: endocrine disruption/fetus/oral contraceptive/prostate/testes

5 To whom correspondence should be addressed at: Wildlife and Contaminant–World Wildlife Fund, 1250 24th Street,NW Washington DC 20037, USA. E-mail: kristina.thayer{at}wwfus.org


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
Toxicol SciHome page
E. Mathews, T. D. Braden, C. S. Williams, J. W. Williams, O. Bolden-Tiller, and H. O. Goyal
Mal-Development of the Penis and Loss of Fertility in Male Rats Treated Neonatally with Female Contraceptive 17{alpha}-Ethinyl Estradiol: A Dose-Response Study and a Comparative Study with a Known Estrogenic Teratogen Diethylstilbestrol
Toxicol. Sci., December 1, 2009; 112(2): 331 - 343.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
B. P. Hermann, M. Sukhwani, D. R. Simorangkir, T. Chu, T. M. Plant, and K. E. Orwig
Molecular dissection of the male germ cell lineage identifies putative spermatogonial stem cells in rhesus macaques
Hum. Reprod., July 1, 2009; 24(7): 1704 - 1716.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
C Harini, S B Sainath, and P S. Reddy
Recovery of suppressed male reproduction in mice exposed to progesterone during embryonic development by testosterone
Reproduction, March 1, 2009; 137(3): 439 - 448.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
D. Della Seta, F. Farabollini, F. Dessi-Fulgheri, and L. Fusani
Environmental-Like Exposure to Low Levels of Estrogen Affects Sexual Behavior and Physiology of Female Rats
Endocrinology, November 1, 2008; 149(11): 5592 - 5598.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
F. S. vom Saal
Could hormone residues be involved?
Hum. Reprod., June 1, 2007; 22(6): 1503 - 1505.
[Full Text] [PDF]


Home page
EndocrinologyHome page
W. V. Welshons, S. C. Nagel, and F. S. vom Saal
Large Effects from Small Exposures. III. Endocrine Mechanisms Mediating Effects of Bisphenol A at Levels of Human Exposure
Endocrinology, June 1, 2006; 147(6): s56 - s69.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
S. Katayama, K. Ashizawa, T. Fukuhara, M. Hiroyasu, Y. Tsuzuki, H. Tatemoto, T. Nakada, and K. Nagai
Differential Expression Patterns of Wnt and {beta}-Catenin/TCF Target Genes in the Uterus of Immature Female Rats Exposed to 17{alpha}-Ethynyl Estradiol
Toxicol. Sci., June 1, 2006; 91(2): 419 - 430.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. G. Timms, K. L. Howdeshell, L. Barton, S. Bradley, C. A. Richter, and F. S. vom Saal
Estrogenic chemicals in plastic and oral contraceptives disrupt development of the fetal mouse prostate and urethra
PNAS, May 10, 2005; 102(19): 7014 - 7019.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
E. V. Younglai, A. C. Holloway, and W. G. Foster
Environmental and occupational factors affecting fertility and IVF success
Hum. Reprod. Update, January 1, 2005; 11(1): 43 - 57.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
H.O. Goyal, A. Robateau, T.D. Braden, C.S. Williams, K.K. Srivastava, and K. Ali
Neonatal Estrogen Exposure of Male Rats Alters Reproductive Functions at Adulthood
Biol Reprod, June 1, 2003; 68(6): 2081 - 2091.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
P. McManamny, H. S. Chy, D. I. Finkelstein, R. G. Craythorn, P. J. Crack, I. Kola, S. S. Cheema, M. K. Horne, N. G. Wreford, M. K. O'Bryan, et al.
A mouse model of spinal and bulbar muscular atrophy
Hum. Mol. Genet., September 1, 2002; 11(18): 2103 - 2111.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
B. G. Timms, R. E. Peterson, and F. S. vom Saal
2,3,7,8-Tetrachlorodibenzo-p-dioxin Interacts with Endogenous Estradiol to Disrupt Prostate Gland Morphogenesis in Male Rat Fetuses
Toxicol. Sci., June 1, 2002; 67(2): 264 - 274.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
M. Joffe
Myths about endocrine disruption and the male reproductive system should not be propagated
Hum. Reprod., February 1, 2002; 17(2): 520 - 521.
[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.