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dc.contributor.authorNugraha, Boya-
dc.contributor.authorYoon, Aerin-
dc.contributor.authorKandagaddala, Lakshmi Devi-
dc.contributor.authorCho, Hyo Joo-
dc.contributor.authorChung, Bong Chul-
dc.contributor.authorKwon, Oh-Seung-
dc.date.accessioned2024-01-20T21:34:15Z-
dc.date.available2024-01-20T21:34:15Z-
dc.date.created2021-09-03-
dc.date.issued2009-04-
dc.identifier.issn1976-9148-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/132608-
dc.description.abstractThis work was conducted to investigate the effect of bisphenol A (BPA) on estradiol (E2) 2-and 4-hydroxylase activities in the liver, kidney and lung tissues of male and female rats. After intraperitoneal administration of BPA to male and female rats for 4 days at 0, 10, and 50 mg/kg, the conversion of the substrate for hepatic and extra-hepatic enzyme activities was measured by GC/MSD. The result showed decreases of body and organ weights at 50 mg/kg BPA of male and female rats. Male hepatic E2 2-hydroxylase activity was inhibited by 68% at 10 mg/kg and by 82% at 50 mg/kg BPA. Female hepatic E2 2-hydroxylase activity was decreased by 46% at 10 mg/kg and by 56% at 50 mg/kg to the control. E2 4-hydroxylase was inhibited by 57 and 57% at 10 mg/kg and 54 and 78% at 50 mg/kg in liver of female and male, respectively. The urinary excretion rate of 2-hydroxyestradiol (2-OHE), androsterone and testosterone in urine of female rats with 50 mg/kg BPA were decreased significantly. The results showed that 50 mg/kg BPA was decreased E2 2-and 4-hydroxylase activities in liver, but not in other tissues. The urinary excretion rates of 2-OHE, androsterone and testosterone were also decreased. In liver, estrogenic enzyme activity were higher in male than female. These results suggest that BPA can disrupt estrogen metabolism by suppressing E2 2-and 4-hydroxylase activities in the liver of male and female rats.-
dc.languageEnglish-
dc.publisherKOREAN SOC APPLIED PHARMACOLOGY-
dc.titleIn Vivo Suppression of Bisphenol A on Estradiol 2-and 4-Hydroxylase Activities in Hepatic Microsomal Fractions of Male and Female Sprague-Dawley Rats-
dc.typeArticle-
dc.identifier.doi10.4062/biomolther.2009.17.2.188-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOMOLECULES & THERAPEUTICS, v.17, no.2, pp.188 - 198-
dc.citation.titleBIOMOLECULES & THERAPEUTICS-
dc.citation.volume17-
dc.citation.number2-
dc.citation.startPage188-
dc.citation.endPage198-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001338751-
dc.identifier.wosid000266067200012-
dc.identifier.scopusid2-s2.0-69549116182-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusESTROGEN-RECEPTOR-ALPHA-
dc.subject.keywordPlusLIVER-MICROSOMES-
dc.subject.keywordPlusCYTOCHROME-P450 ISOFORMS-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlus17-BETA-ESTRADIOL-
dc.subject.keywordPlusVITRO-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlus2-METHOXYESTRADIOL-
dc.subject.keywordPlusANGIOGENESIS-
dc.subject.keywordAuthorBisphenol A-
dc.subject.keywordAuthorEstradiol 2-hydroxylase-
dc.subject.keywordAuthorEstradiol 4-hydroxylase-
dc.subject.keywordAuthorEstrogen metabolites-
dc.subject.keywordAuthorRat-
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