Literature DB >> 10536108

Normal reproductive organ development in Wistar rats exposed to bisphenol A in the drinking water.

S Z Cagen1, J M Waechter, S S Dimond, W J Breslin, J H Butala, F W Jekat, R L Joiner, R N Shiotsuka, G E Veenstra, L R Harris.   

Abstract

Bisphenol A (BPA) is a chemical used primarily as a monomer in the manufacture of numerous chemical products, such as epoxy resins and polycarbonate. The objective of this study was to evaluate potential effects of BPA on sexual development of male rats and was designed to clarify low-dose observations reported as preliminary results by Sharpe et al. (1996). The protocol for the present study followed the same treatment schedule as reported by Sharpe et al. (1995, 1996), but included more treatment groups, a greater number of animals per group, and a more comprehensive number of reproductive endpoints. Groups of 28 female Han-Wistar albino rats were exposed to drinking water that contained 0, 0.01, 0.1, 1.0, or 10 ppm BPA or 0.1 ppm diethylstilbestrol (DES), 7 days per week, for a total of 10 weeks. Treatment of the females began at 10 weeks of age and continued throughout a 2-week premating period, 2 weeks of mating (to untreated males), 21-22 days of gestation, and 22 days of lactation. Offspring weanling males were given untreated drinking water and maintained until 90 days of age when evaluations were made of various reproductive organs. Consistent with Sharpe et al. (1996) the female offspring were not evaluated. No treatment-related effects on growth or reproductive endpoints were observed in adult females exposed to any concentration of BPA. Similarly, no treatment-related effects were observed on the growth, survival, or reproductive parameters (including testes, prostate and preputial gland weights, sperm count, daily sperm production, or testes histopathology) of male offspring from dams exposed to BPA during gestation and lactation. DES administered in the drinking water at 0. 1 ppm resulted in decreased body weight, body weight change, and food consumption in adult females. In addition, an increase in the duration of gestation and a decrease in the number of pups delivered and number of live pups were also observed in animals exposed to DES. In conclusion, these results do not confirm the previous findings of Sharpe et al. (1996) and show that low doses of BPA had no effects on male sexual development in the rat. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10536108     DOI: 10.1006/rtph.1999.1340

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  19 in total

1.  Reduced sperm counts in guppies (Poecilia reticulata) following exposure to low levels of tributyltin and bisphenol A.

Authors:  E Haubruge; F Petit; M J Gage
Journal:  Proc Biol Sci       Date:  2000-11-22       Impact factor: 5.349

Review 2.  Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses.

Authors:  Laura N Vandenberg; Theo Colborn; Tyrone B Hayes; Jerrold J Heindel; David R Jacobs; Duk-Hee Lee; Toshi Shioda; Ana M Soto; Frederick S vom Saal; Wade V Welshons; R Thomas Zoeller; John Peterson Myers
Journal:  Endocr Rev       Date:  2012-03-14       Impact factor: 19.871

3.  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

4.  Probable gamma-aminobutyric acid involvement in bisphenol A effect at the hypothalamic level in adult male rats.

Authors:  Nancy Cardoso; Matías Pandolfi; Justina Lavalle; Silvia Carbone; Osvaldo Ponzo; Pablo Scacchi; Roxana Reynoso
Journal:  J Physiol Biochem       Date:  2011-06-09       Impact factor: 4.158

5.  Effects of endocrine disruptors on prosobranch snails (Mollusca: Gastropoda) in the laboratory. Part I: Bisphenol A and octylphenol as xeno-estrogens.

Authors:  J Oehlmann; U Schulte-Oehlmann; M Tillmann; B Markert
Journal:  Ecotoxicology       Date:  2000-12       Impact factor: 2.823

6.  Daily urinary excretion of bisphenol A.

Authors:  Chikako Arakawa; Kayumi Fujimaki; Jun Yoshinaga; Hideki Imai; Shigeko Serizawa; Hiroaki Shiraishi
Journal:  Environ Health Prev Med       Date:  2004-01       Impact factor: 3.674

7.  High butter-fat diet and bisphenol A additively impair male rat spermatogenesis.

Authors:  Pheruza Tarapore; Max Hennessy; Dan Song; Jun Ying; Bin Ouyang; Vinothini Govindarajah; Yuet-Kin Leung; Shuk-Mei Ho
Journal:  Reprod Toxicol       Date:  2016-09-19       Impact factor: 3.143

8.  The politics of plastics: the making and unmaking of bisphenol a "safety".

Authors:  Sarah A Vogel
Journal:  Am J Public Health       Date:  2009-11       Impact factor: 9.308

Review 9.  In vivo effects of bisphenol A in laboratory rodent studies.

Authors:  Catherine A Richter; Linda S Birnbaum; Francesca Farabollini; Retha R Newbold; Beverly S Rubin; Chris E Talsness; John G Vandenbergh; Debby R Walser-Kuntz; Frederick S vom Saal
Journal:  Reprod Toxicol       Date:  2007-06-26       Impact factor: 3.143

Review 10.  The estrogenic content of rodent diets, bedding, cages, and water bottles and its effect on bisphenol A studies.

Authors:  Julius E Thigpen; Kenneth D R Setchell; Grace E Kissling; Jacqueline Locklear; Gordon F Caviness; Tanya Whiteside; Scott M Belcher; Nadine M Brown; Bradley J Collins; Fred B Lih; Kenneth B Tomer; Elizabeth Padilla-Banks; Luísa Camacho; Floyd G Adsit; Mary Grant
Journal:  J Am Assoc Lab Anim Sci       Date:  2013-03       Impact factor: 1.232

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