Literature DB >> 11780958

Rat two-generation reproductive toxicity study of bisphenol A.

M Ema1, S Fujii, M Furukawa, M Kiguchi, T Ikka, A Harazono.   

Abstract

This study was conducted to determine the low-dose effects of bisphenol A (BPA) in a rat two-generation reproduction study. Groups of 25 male and 25 female Crj: CD (SD) IGS rats were given BPA at 0.2, 2, 20, or 200 microg/kg/day by gastric intubation throughout the study beginning at the onset of a 10- and 2-week premating period, in F0 males and females, respectively, and continuing through the mating, gestation, and lactation periods, for two generations. There were adult (F0, F1, F2) and postnatal day (PND) 22 (F1, F2) necropsies: the oldest F2 males and females being killed at postnatal weeks 7 and 14, respectively. No compound-related clinical signs or effects on body weight or food consumption were observed in any generation. There were no compound-related changes in surface righting reflex, negative geotaxis reflex, mid-air righting reflex, pinna detachment, incisor eruption, eye opening, testes descent, preputial separation, or vaginal opening in F1 and F2 generations, or behavior in the open field or water filled multiple T-maze in the F1 generation. No test compound-related changes in estrous cyclicity, copulation index, fertility index, number of implantations, gestation length, litter size, pup weight, pup sex ratio, pup viability, or other functional reproductive measures were noted in any generation. A few significant changes in the anogenital distance (AGD) per cube root of body weight ratio were found at 0.2 and 20 microg/kg in F1 males, at 2, 20, and 200 microg/kg in F1 females, and at 20 and 200 microg/kg in F2 females. However, the changes in the AGD were consistently small (within 5% of control values), and no continuous changes in the AGD or AGD/cube root of body weight ratio were detected. There were no compound-related changes in epididymal sperm counts or motility in F0 and F1 males. No compound-related necropsy findings or effects on organ weight including the reproductive organs were found in any generation. Histopathologic examinations revealed no evidence of compound-related changes in any organs including the reproductive organs of both sexes. The data indicate that oral doses of BPA of between 0.2 and 200 microg/kg over 2 generations did not cause significant compound-related changes in reproductive or developmental parameters in rats.

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Year:  2001        PMID: 11780958     DOI: 10.1016/s0890-6238(01)00160-5

Source DB:  PubMed          Journal:  Reprod Toxicol        ISSN: 0890-6238            Impact factor:   3.143


  29 in total

Review 1.  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

2.  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

3.  Effects of perinatal bisphenol A exposure during early development on radial arm maze behavior in adult male and female rats.

Authors:  Renee N Sadowski; Pul Park; Steven L Neese; Duncan C Ferguson; Susan L Schantz; Janice M Juraska
Journal:  Neurotoxicol Teratol       Date:  2014-01-17       Impact factor: 3.763

4.  Effects of Water Bottle Materials and Filtration on Bisphenol A Content in Laboratory Animal Drinking Water.

Authors:  Jennifer A Honeycutt; Jenny Q T Nguyen; Amanda C Kentner; Heather C Brenhouse
Journal:  J Am Assoc Lab Anim Sci       Date:  2017-05-01       Impact factor: 1.232

Review 5.  Early programing of uterine tissue by bisphenol A: Critical evaluation of evidence from animal exposure studies.

Authors:  Alexander Suvorov; David J Waxman
Journal:  Reprod Toxicol       Date:  2015-05-28       Impact factor: 3.143

6.  Developmental neurotoxicity study of dietary bisphenol A in Sprague-Dawley rats.

Authors:  Donald G Stump; Melissa J Beck; Ann Radovsky; Robert H Garman; Lester L Freshwater; Larry P Sheets; M Sue Marty; John M Waechter; Stephen S Dimond; John P Van Miller; Ronald N Shiotsuka; Dieter Beyer; Anne H Chappelle; Steven G Hentges
Journal:  Toxicol Sci       Date:  2010-02-17       Impact factor: 4.849

7.  Bisphenol A prevents the synaptogenic response to estradiol in hippocampus and prefrontal cortex of ovariectomized nonhuman primates.

Authors:  Csaba Leranth; Tibor Hajszan; Klara Szigeti-Buck; Jeremy Bober; Neil J MacLusky
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-03       Impact factor: 11.205

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

9.  Toxicity evaluation of bisphenol A administered by gavage to Sprague Dawley rats from gestation day 6 through postnatal day 90.

Authors:  K Barry Delclos; Luísa Camacho; Sherry M Lewis; Michelle M Vanlandingham; John R Latendresse; Greg R Olson; Kelly J Davis; Ralph E Patton; Gonçalo Gamboa da Costa; Kellie A Woodling; Matthew S Bryant; Mani Chidambaram; Raul Trbojevich; Beth E Juliar; Robert P Felton; Brett T Thorn
Journal:  Toxicol Sci       Date:  2014-02-04       Impact factor: 4.849

10.  Basic exploratory research versus guideline-compliant studies used for hazard evaluation and risk assessment: bisphenol A as a case study.

Authors:  Rochelle W Tyl
Journal:  Environ Health Perspect       Date:  2009-06-29       Impact factor: 9.031

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