Hormonal activity of combinations of genistein, bisphenol A and 17beta-estradiol in the female Wistar rat
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 17beta-estradiol in vivo, is limited. Therefore, the combinatory activity of th...
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description | 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 17beta-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 microg, 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 ERbeta have to be characterized in further investigations. |
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However, information about their activity in combination with xenoestrogens and 17beta-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 microg, 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 ERbeta have to be characterized in further investigations.</description><identifier>ISSN: 0340-5761</identifier><identifier>PMID: 16639590</identifier><language>eng</language><publisher>Germany</publisher><subject><![CDATA[Administration, Oral ; Animals ; Benzhydryl Compounds ; Clusterin - genetics ; Clusterin - metabolism ; Complement C3 - genetics ; Complement C3 - metabolism ; Drug Interactions ; Epithelial Cells - drug effects ; Estradiol - analogs & derivatives ; Estradiol - metabolism ; Estradiol - pharmacology ; Estrogen Antagonists - pharmacology ; Estrogens - administration & dosage ; Estrogens - pharmacology ; Ethinyl Estradiol - administration & dosage ; Ethinyl Estradiol - pharmacology ; Female ; Gene Expression - drug effects ; Genistein - administration & dosage ; Genistein - pharmacology ; Organ Size - drug effects ; Ovariectomy ; Phenols - administration & dosage ; Phenols - pharmacology ; Phytoestrogens - administration & dosage ; Phytoestrogens - pharmacology ; Rats ; Rats, Wistar ; RNA, Messenger - metabolism ; Uterus - cytology ; Uterus - drug effects ; Uterus - growth & development ; Uterus - metabolism ; Vagina - cytology ; Vagina - drug effects]]></subject><ispartof>Archives of toxicology, 2006-12, Vol.80 (12), p.839</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16639590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmidt, Simone</creatorcontrib><creatorcontrib>Degen, Gisela H</creatorcontrib><creatorcontrib>Seibel, Jan</creatorcontrib><creatorcontrib>Hertrampf, Torsten</creatorcontrib><creatorcontrib>Vollmer, Günter</creatorcontrib><creatorcontrib>Diel, Patrick</creatorcontrib><title>Hormonal activity of combinations of genistein, bisphenol A and 17beta-estradiol in the female Wistar rat</title><title>Archives of toxicology</title><addtitle>Arch Toxicol</addtitle><description>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 17beta-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 microg, 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 ERbeta have to be characterized in further investigations.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Benzhydryl Compounds</subject><subject>Clusterin - genetics</subject><subject>Clusterin - metabolism</subject><subject>Complement C3 - genetics</subject><subject>Complement C3 - metabolism</subject><subject>Drug Interactions</subject><subject>Epithelial Cells - drug effects</subject><subject>Estradiol - analogs & derivatives</subject><subject>Estradiol - metabolism</subject><subject>Estradiol - pharmacology</subject><subject>Estrogen Antagonists - pharmacology</subject><subject>Estrogens - administration & dosage</subject><subject>Estrogens - pharmacology</subject><subject>Ethinyl Estradiol - administration & dosage</subject><subject>Ethinyl Estradiol - pharmacology</subject><subject>Female</subject><subject>Gene Expression - drug effects</subject><subject>Genistein - administration & dosage</subject><subject>Genistein - pharmacology</subject><subject>Organ Size - drug effects</subject><subject>Ovariectomy</subject><subject>Phenols - administration & dosage</subject><subject>Phenols - pharmacology</subject><subject>Phytoestrogens - administration & dosage</subject><subject>Phytoestrogens - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>RNA, Messenger - metabolism</subject><subject>Uterus - cytology</subject><subject>Uterus - drug effects</subject><subject>Uterus - growth & development</subject><subject>Uterus - metabolism</subject><subject>Vagina - cytology</subject><subject>Vagina - drug effects</subject><issn>0340-5761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j8FKAzEYhHNQbK2-guQBXEia3WRzLEWtUOil4LH8Sf7YyG6yJFHo27uinoYZ-IaZK7JkomVNpyRfkNtSPhjj616LG7LgUgrdabYkYZfymCIMFGwNX6FeaPLUptGECDWkWH78O8ZQKob4SE0o0xljGuiGQnSUK4MVGiw1gwtzHCKtZ6QeRxiQvs0cZJqh3pFrD0PB-z9dkePz03G7a_aHl9ftZt9M3by2V9oIg1o556WxznFtuLey0712AjxDa7gFoXivXCsdtq1kymvnuVm3WosVefitnT7NiO405TBCvpz-L4tvUIFTSA</recordid><startdate>200612</startdate><enddate>200612</enddate><creator>Schmidt, Simone</creator><creator>Degen, Gisela H</creator><creator>Seibel, Jan</creator><creator>Hertrampf, Torsten</creator><creator>Vollmer, Günter</creator><creator>Diel, Patrick</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>200612</creationdate><title>Hormonal activity of combinations of genistein, bisphenol A and 17beta-estradiol in the female Wistar rat</title><author>Schmidt, Simone ; Degen, Gisela H ; Seibel, Jan ; Hertrampf, Torsten ; Vollmer, Günter ; Diel, Patrick</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p540-879b3be97ddf6bcdd19b1fc65989d3af0ecb1ca37187d46de44607f9df1b24993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Benzhydryl Compounds</topic><topic>Clusterin - genetics</topic><topic>Clusterin - metabolism</topic><topic>Complement C3 - genetics</topic><topic>Complement C3 - metabolism</topic><topic>Drug Interactions</topic><topic>Epithelial Cells - drug effects</topic><topic>Estradiol - analogs & derivatives</topic><topic>Estradiol - metabolism</topic><topic>Estradiol - pharmacology</topic><topic>Estrogen Antagonists - pharmacology</topic><topic>Estrogens - administration & dosage</topic><topic>Estrogens - pharmacology</topic><topic>Ethinyl Estradiol - administration & dosage</topic><topic>Ethinyl Estradiol - pharmacology</topic><topic>Female</topic><topic>Gene Expression - drug effects</topic><topic>Genistein - administration & dosage</topic><topic>Genistein - pharmacology</topic><topic>Organ Size - drug effects</topic><topic>Ovariectomy</topic><topic>Phenols - administration & dosage</topic><topic>Phenols - pharmacology</topic><topic>Phytoestrogens - administration & dosage</topic><topic>Phytoestrogens - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>RNA, Messenger - metabolism</topic><topic>Uterus - cytology</topic><topic>Uterus - drug effects</topic><topic>Uterus - growth & development</topic><topic>Uterus - metabolism</topic><topic>Vagina - cytology</topic><topic>Vagina - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmidt, Simone</creatorcontrib><creatorcontrib>Degen, Gisela H</creatorcontrib><creatorcontrib>Seibel, Jan</creatorcontrib><creatorcontrib>Hertrampf, Torsten</creatorcontrib><creatorcontrib>Vollmer, Günter</creatorcontrib><creatorcontrib>Diel, Patrick</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Archives of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmidt, Simone</au><au>Degen, Gisela H</au><au>Seibel, Jan</au><au>Hertrampf, Torsten</au><au>Vollmer, Günter</au><au>Diel, Patrick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hormonal activity of combinations of genistein, bisphenol A and 17beta-estradiol in the female Wistar rat</atitle><jtitle>Archives of toxicology</jtitle><addtitle>Arch Toxicol</addtitle><date>2006-12</date><risdate>2006</risdate><volume>80</volume><issue>12</issue><spage>839</spage><pages>839-</pages><issn>0340-5761</issn><abstract>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 17beta-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 microg, 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 ERbeta have to be characterized in further investigations.</abstract><cop>Germany</cop><pmid>16639590</pmid></addata></record> |
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subjects | Administration, Oral Animals Benzhydryl Compounds Clusterin - genetics Clusterin - metabolism Complement C3 - genetics Complement C3 - metabolism Drug Interactions Epithelial Cells - drug effects Estradiol - analogs & derivatives Estradiol - metabolism Estradiol - pharmacology Estrogen Antagonists - pharmacology Estrogens - administration & dosage Estrogens - pharmacology Ethinyl Estradiol - administration & dosage Ethinyl Estradiol - pharmacology Female Gene Expression - drug effects Genistein - administration & dosage Genistein - pharmacology Organ Size - drug effects Ovariectomy Phenols - administration & dosage Phenols - pharmacology Phytoestrogens - administration & dosage Phytoestrogens - pharmacology Rats Rats, Wistar RNA, Messenger - metabolism Uterus - cytology Uterus - drug effects Uterus - growth & development Uterus - metabolism Vagina - cytology Vagina - drug effects |
title | Hormonal activity of combinations of genistein, bisphenol A and 17beta-estradiol in the female Wistar rat |
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