Normal sexual development of two strains of rat exposed in utero to low doses of bisphenol A

被引:90
作者
Tinwell, H
Haseman, J
Lefevre, PA
Wallis, N
Ashby, J
机构
[1] Syngenta Cent Toxicol Lab, Macclesfield SK10 4TJ, Cheshire, England
[2] NIEHS, Res Triangle Pk, NC 27709 USA
关键词
bisphenol A; Sprague-Dawley rats; Alderley Park rats; sexual development; in utero exposure;
D O I
10.1093/toxsci/68.2.339
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Pregnant Sprague-Dawley (SD) and Alderley Park (Wistar derived) rats were exposed by gavage during gestation days 6-21 to 20 mug/kg, 100 mug/kg, or 50 mg/kg body weight of BPA with ethinylestradiol (EE; 200 mug/kg) acting as a positive control agent. The sexual development of the derived pups was monitored until termination at postnatal day 90-98. The endpoints evaluated were litter size and weight, anogenital distance at birth, days of vaginal opening, first estrus and prepuce separation, weights of the liver, seminal vesicles, epididimydes, testes, ventral prostate, uterus, vagina, cervix and ovaries, and daily sperm production. Males were terminated at postnatal day 90 and females at postnatal day 98. The only statistically significant effects observed for any dose of BPA were a decrease in daily sperm production and an increase in the age of vaginal opening for the Alderley Park animals at the highest dose evaluated (50 mg/kg). The dose of EE evaluated proved to be maternally toxic in our laboratory, but provided gross evidence of endocrine disruption in the treated dams. These results diverge from those of Chahoud and his colleagues who indicated disturbances to the sexual development of both male and female SD rat pups administered the same 3 doses of BPA. This failure to confirm low dose endocrine effects for BPA is discussed within the context of similar divergent conclusions derived from other assessments of the endocrine toxicity of this agent to rats.
引用
收藏
页码:339 / 348
页数:10
相关论文
共 33 条
[1]   Increasing the sensitivity of the rodent uterotrophic assay to estrogens, with particular reference to bisphenol A [J].
Ashby, J .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2001, 109 (11) :1091-1094
[2]   Normal sexual development of rats exposed to butyl benzyl phthalate from conception to weaning [J].
Ashby, J ;
Tinwell, H ;
Lefevre, PA ;
Odum, J ;
Paton, D ;
Millward, SW ;
Tittensor, S ;
Brooks, AN .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1997, 26 (01) :102-118
[3]   Getting the problem of endocrine disruption into focus: The need for a pause for thought [J].
Ashby, J .
APMIS, 2000, 108 (12) :805-813
[4]  
Ashby J, 2000, J APPL TOXICOL, V20, P35, DOI 10.1002/(SICI)1099-1263(200001/02)20:1<35::AID-JAT633>3.3.CO
[5]  
2-#
[6]   Comparative effects of neonatal exposure of male rats to potent and weak (environmental) estrogens on spermatogenesis at puberty and the relationship to adult testis size and fertility: Evidence for stimulatory effects of low estrogen levels [J].
Atanassova, N ;
McKinnell, C ;
Turner, KJ ;
Walker, M ;
Fisher, JS ;
Morley, M ;
Millar, MR ;
Groome, NP ;
Sharpe, RM .
ENDOCRINOLOGY, 2000, 141 (10) :3898-3907
[7]  
Blazak WF, 1993, METHODS TOXICOLOGY A, V3, P86, DOI DOI 10.1016/B978-0-12-461207-5.50009-2
[8]   Normal reproductive organ development in Wister rats exposed to Bisphenol A in the drinking water [J].
Cagen, SZ ;
Waechter, JM ;
Dimond, SS ;
Breslin, WJ ;
Butala, JH ;
Jekat, FW ;
Joiner, RL ;
Shiotsuka, RN ;
Veenstra, GE ;
Harris, LR .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1999, 30 (02) :130-139
[9]  
Chahoud I., 2001, REPROD TOXICOL, V15, P589
[10]  
ELSWICK BA, 2000, TOXICOLOGIST, V54, P256