Literature DB >> 2874623

Leydig cell hyperplasia in fetal mice treated transplacentally with ethinyl estradiol.

Y Yasuda, H Konishi, T Tanimura.   

Abstract

Pregnant female mice were given ethinyl estradiol on days 11 through 17 of gestation. On day 18 the dams were killed and the male fetuses were examined for testicular differentiation. Three of 12 males from dams treated with the highest dose of ethinyl estradiol showed cryptorchid testes with uterine tubes. Light and electron microscopic evaluation of the testes, both cryptorchid and normal, demonstrated foci of hyperplasia of Leydig cells showing cytoplasmic and nuclear pleomorphism, increase in lipid droplets, and decrease in smooth endoplasmic reticulum and ribosomes when compared to testes from control fetal mice. Morphometric determinations of the testes indicated that the number of Leydig cells in a unit area (mm2) in the interstitial tissue showed a dose-response relationship to ethinyl estradiol in the normal testes. The number of Leydig cells in the testes exposed to the highest dose of estrogen showed a significant difference between cryptorchid and normal testes: the former had fewer Leydig cells than the latter. These morphological observations indicate that hyperplasia of Leydig cells of fetal mouse testis at term can be induced by transplacental treatment with ethinyl estradiol and suggest that a malignant transformation into a Leydig cell tumor is possible.

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Year:  1986        PMID: 2874623     DOI: 10.1002/tera.1420330305

Source DB:  PubMed          Journal:  Teratology        ISSN: 0040-3709


  7 in total

1.  Rebuttal of "Flawed Experimental Design Reveals the Need for Guidelines Requiring Appropriate Positive Controls in Endocrine Disruption Research" by (Vom Saal 2010).

Authors:  Leon Earl Gray; Bryce Ryan; Andrew K Hotchkiss; Kevin M Crofton
Journal:  Toxicol Sci       Date:  2010-03-05       Impact factor: 4.849

2.  Transplacental carcinogenesis with dibenzo[def,p]chrysene (DBC): timing of maternal exposures determines target tissue response in offspring.

Authors:  Lyndsey E Shorey; David J Castro; William M Baird; Lisbeth K Siddens; Christiane V Löhr; Melissa M Matzke; Katrina M Waters; Richard A Corley; David E Williams
Journal:  Cancer Lett       Date:  2011-11-13       Impact factor: 8.679

3.  Effect of prenatal exposure to hydroxyprogesterone on steroidogenic enzymes in male rats.

Authors:  T Pushpalatha; P Ramachandra Reddy; P Sreenivasula Reddy
Journal:  Naturwissenschaften       Date:  2002-12-20

4.  Overlapping but distinct effects of genistein and ethinyl estradiol (EE(2)) in female Sprague-Dawley rats in multigenerational reproductive and chronic toxicity studies.

Authors:  K Barry Delclos; Constance C Weis; Thomas J Bucci; Greg Olson; Paul Mellick; Natalya Sadovova; John R Latendresse; Brett Thorn; Retha R Newbold
Journal:  Reprod Toxicol       Date:  2008-12-30       Impact factor: 3.143

5.  Accelerated differentiation in seminiferous tubules of fetal mice prenatally exposed to ethinyl estradiol.

Authors:  Y Yasuda; H Konishi; T Matuso; T Tanimura
Journal:  Anat Embryol (Berl)       Date:  1986

6.  Mal-development of the penis and loss of fertility in male rats treated neonatally with female contraceptive 17alpha-ethinyl estradiol: a dose-response study and a comparative study with a known estrogenic teratogen diethylstilbestrol.

Authors:  Ensa Mathews; Tim D Braden; Carol S Williams; John W Williams; Olga Bolden-Tiller; Hari O Goyal
Journal:  Toxicol Sci       Date:  2009-09-03       Impact factor: 4.849

7.  The effect of in utero ethinyl oestradiol exposure on the risk of cryptorchid testis and testicular teratoma in mice.

Authors:  A H Walker; L Bernstein; D W Warren; N E Warner; X Zheng; B E Henderson
Journal:  Br J Cancer       Date:  1990-10       Impact factor: 7.640

  7 in total

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