Hormonal activity of combinations of genistein, bisphenol A and 17β-estradiol in the female Wistar rat

被引:32
作者
Schmidt, Simone
Degen, Gisela H.
Seibel, Jan
Hertrampf, Torsten
Vollmer, Guenter
Diel, Patrick
机构
[1] Deutsch Sporthsch, Inst Kreislaufforsch & Sportmed, Abt Mol & Zellulare Sportmed, D-50933 Cologne, Germany
[2] Univ Dortmund, Inst Arbeitsphysiol, D-44221 Dortmund, Germany
[3] Tech Univ Dresden, Lehrstuhl Mol & Zellulare Endokrinol, Inst Zool, D-8027 Dresden, Germany
关键词
Bisphenol A; Phytoestrogens; Genistein; Combinatory action;
D O I
10.1007/s00204-006-0102-4
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Phytoestrogens have been described as weak estrogens,selective estrogen receptor mediators (SERMs) or to exhibit antiestrogenic properties. However, information about their activity in combination with xenoestrogens and 17 beta-estradiol in vivo, is limited. Therefore, the combinatory activity of the phytoestrogen genistein (Gen), the industrial chemical bisphenol A (BPA), and ethinylestradiol (EE) in ovariectomized Wistar rats was analyzed in this study. All compounds were administered orally on three consecutive days (EE at 30 mu g, Gen at 100 mg and BPA at 200 mg per kg body weight per day). The pure antiestrogen fulvestrant (3 mg/kg) served as estrogen receptor (ER) antagonist control. Effects on uterine wet weight, height of the uterine epithelium, uterine clusterin (Clu) and complement C3 expression, and the height of the vaginal epithelium were examined. Treatment with Gen alone resulted in a moderate stimulation of uterine weight; in the vagina the height of the epithelium was strongly stimulated. BPA did not stimulate any of the above-mentioned parameters significantly. In combination with EE, Gen acted on most of the analyzed parameters in an additive manner, whereas BPA significantly antagonized the effects of EE on the uterine epithelium and uterine Clu expression. Given in combination with Gen, BPA was also able to antagonize the stimulatory effect of Gen on the uterine epithelium. In summary, our results demonstrate that Gen, in contrast to BPA, does not exhibit any antiestrogenic properties, even if given at high concentrations. The results of this study characterize BPA as a functional antiestrogen, very likely the result of a lack of ability to activate ER-mediated transactivation after binding to the receptor. This is not the case for Gen. Our results point to the involvement of complex molecular mechanisms in the action of Gen. These mechanisms, especially the role of ER beta have to be characterized in further investigations.
引用
收藏
页码:839 / 845
页数:7
相关论文
共 39 条
[1]   Phytoestrogens and breast cancer [J].
Adlercreutz, H .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2002, 83 (1-5) :113-118
[2]   Dual effects of phytoestrogens result in U-shaped dose-response curves [J].
Almstrup, K ;
Fernández, MF ;
Petersen, JH ;
Olea, N ;
Skakkebaek, NE ;
Leffers, H .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2002, 110 (08) :743-748
[3]   Health potential of soy isoflavones for menopausal women [J].
Anderson, John J. B. ;
Anthony, Mary S. ;
Cline, J. Mark ;
Washburn, Scott A. ;
Garner, Sanford C. .
PUBLIC HEALTH NUTRITION, 1999, 2 (04) :489-504
[4]   A realistic clinical perspective of tamoxifen and endometrial carcinogenesis [J].
Assikis, VJ ;
Neven, P ;
Jordan, VC ;
Vergote, I .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (09) :1464-1476
[5]  
Cline J M, 1998, Cancer Treat Res, V94, P107
[6]   Tissue distribution and quantitative analysis of estrogen receptor-alpha (ER alpha) and estrogen receptor-beta (ER beta) messenger ribonucleic acid in the wild-type and ER alpha-knockout mouse [J].
Couse, JF ;
Lindzey, J ;
Grandien, K ;
Gustafsson, JA ;
Korach, KS .
ENDOCRINOLOGY, 1997, 138 (11) :4613-4621
[7]  
Davis SR, 1999, RECENT PROG HORM RES, V54, P185
[8]   Estrogenic isoflavones in rodent diets [J].
Degen, GH ;
Janning, P ;
Diel, P ;
Bolt, HM .
TOXICOLOGY LETTERS, 2002, 128 (1-3) :145-157
[9]   Ability of xeno- and phytoestrogens to modulate expression of estrogen-sensitive genes in rat uterus: estrogenicity profiles and uterotropic activity [J].
Diel, P ;
Schulz, T ;
Smolnikar, K ;
Strunck, E ;
Vollmer, G ;
Michna, H .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2000, 73 (1-2) :1-10
[10]   Comparative responses of three rat strains (DA/Han, Sprague-Dawley and Wistar) to treatment with environmental estrogens [J].
Diel, P ;
Schmidt, S ;
Vollmer, G ;
Janning, P ;
Upmeier, A ;
Michna, H ;
Bolt, HM ;
Degen, GH .
ARCHIVES OF TOXICOLOGY, 2004, 78 (04) :183-193