dc.contributorUniversidade Federal de Goiás (UFG)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2019-10-06T16:19:15Z
dc.date.accessioned2022-12-19T18:47:03Z
dc.date.available2019-10-06T16:19:15Z
dc.date.available2022-12-19T18:47:03Z
dc.date.created2019-10-06T16:19:15Z
dc.date.issued2019-04-01
dc.identifierReproductive Toxicology, v. 85, p. 83-92.
dc.identifier1873-1708
dc.identifier0890-6238
dc.identifierhttp://hdl.handle.net/11449/188788
dc.identifier10.1016/j.reprotox.2019.02.009
dc.identifier2-s2.0-85062231264
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5369826
dc.description.abstractThis study evaluated the effects of BPS (40 μg/kg/day, during 28 consecutive days) on the male ventral prostate and female prostate of adult gerbils. For comparative purposes, gerbils were also exposed to BPA under the same experimental conditions. The prostates were submitted to biometric, morphometric, histopathological, immunohistochemical and ultrastructural analyses. The results demonstrated that exposure to both types of bisphenol caused no changes in testosterone or estradiol serum levels. Morphologically, the effects of BPS and BPA on female prostates were similar and included changes in prostatic tissue compartments, glandular hyperplasia, AR and ERα up-regulation and increased cell proliferation. In males, BPS and BPA promoted differential effects, since the prostate presented morphological changes and proliferative disorders that were more pronounced in the BPS group. Therefore, this study demonstrates that BPS caused endocrine disruption in the prostate of male and female gerbils.
dc.languageeng
dc.relationReproductive Toxicology
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectAndrogen receptor
dc.subjectEndocrine-disrupting chemicals
dc.subjectEstrogen receptor
dc.subjectMorphology
dc.subjectReproduction
dc.titleBisphenol-S promotes endocrine-disrupting effects similar to those promoted by bisphenol-A in the prostate of adult gerbils
dc.typeArtículos de revistas


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