Large effects from small exposures. II. The importance of positive controls in low-dose research on bisphenol A

被引:208
作者
vom Saal, FS [1 ]
Welshons, WV
机构
[1] Univ Missouri, Div Biol Sci, Columbia, MO 65211 USA
[2] Univ Missouri, Dept Biomed Sci, Columbia, MO 65211 USA
关键词
endocrine-disrupting chemicals; environmental estrogens; DES; bisphenol A; positive controls; low dose;
D O I
10.1016/j.envres.2005.09.001
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Over six-billion pounds per year of the monomer bisphenol A (BPA) are used to manufacture polycarbonate plastic products, resins lining cans, dental sealants, and polyvinyl chloride plastic products. There are 109 published studies as of July 2005 that report significant effects of low doses of BPA in experimental animals, with many adverse effects occurring at blood levels in animals within and below average blood levels in humans; 40 studies report effects below the current reference dose of 50 mu g/kg/day that is still assumed to be safe by the US-FDA and US-EPA in complete disregard of the published findings. The extensive list of significant findings from government-funded studies is compared to the I I published studies that were funded by the chemical industry, 100% of which conclude that BPA causes no significant effects. We discuss the importance of appropriate controls in toxicological research and that positive controls are required to determine whether conclusions from experiments that report no significant effects are valid or false. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:50 / 76
页数:27
相关论文
共 199 条
[91]   Manufacturing uncertainty: Contested science and the protection of the public's health and environment [J].
Michaels, D ;
Monforton, C .
AMERICAN JOURNAL OF PUBLIC HEALTH, 2005, 95 :S39-S48
[92]   Doubt is their product [J].
Michaels, D .
SCIENTIFIC AMERICAN, 2005, 292 (06) :96-101
[93]  
MILLOY S, 2005, CALIFORNIAS BOGUS BA
[94]   SERUM CORTICOSTERONE IN FETAL MICE - SEX-DIFFERENCES, CIRCADIAN CHANGES, AND EFFECT OF MATERNAL STRESS [J].
MONTANO, MM ;
WANG, MH ;
EVEN, MD ;
VOMSAAL, FS .
PHYSIOLOGY & BEHAVIOR, 1991, 50 (02) :323-329
[95]   FREE ESTRADIOL IN SERUM AND BRAIN UPTAKE OF ESTRADIOL DURING FETAL AND NEONATAL SEXUAL-DIFFERENTIATION IN FEMALE RATS [J].
MONTANO, MM ;
WELSHONS, WV ;
VOMSAAL, FS .
BIOLOGY OF REPRODUCTION, 1995, 53 (05) :1198-1207
[96]   Thyroid hormone action is disrupted by bisphenol A as an antagonist [J].
Moriyama, K ;
Tagami, T ;
Akamizu, T ;
Usui, T ;
Saijo, M ;
Kanamoto, N ;
Hataya, Y ;
Shimatsu, A ;
Kuzuya, H ;
Nakao, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (11) :5185-5190
[97]   THE DEVELOPMENTAL TOXICITY OF BISPHENOL-A IN RATS AND MICE [J].
MORRISEY, RE ;
GEORGE, JD ;
PRICE, CJ ;
TYL, RW ;
MARR, MC ;
KIMMEL, CA .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1987, 8 (04) :571-582
[98]  
MUNOZDETORO M, 2005, ENDOCRINOLOGY 0531
[99]   Development of an ER action indicator mouse for the study of estrogens, selective ER modulators (SERMs), and xenobiotics [J].
Nagel, SC ;
Hagelbarger, JL ;
McDonnell, DP .
ENDOCRINOLOGY, 2001, 142 (11) :4721-4728
[100]   Relative binding affinity serum modified access (RBA-SMA) assay predicts the relative in vivo bioactivity of the xenoestrogens bisphenol A and octylphenol [J].
Nagel, SC ;
vomSaal, FS ;
Thayer, KA ;
Dhar, MG ;
Boechler, M ;
Welshons, WV .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1997, 105 (01) :70-76