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A suggested bisphenol A metabolite (MBP) interfered with reproductive organ development in the chicken embryo while a human-relevant mixture of phthalate monoesters had no such effects
Authors:Anna Mentor  Carl-Gustaf Bornehag  Maria Jönsson  Anna Mattsson
Institution:1. Department of Environmental Toxicology, Uppsala University, Uppsala, Sweden;2. Department of Environmental Medicine and Public Health, Centre for Reproductive Biology in Uppsala (CRU), Uppsala, Swedenanna.mentor@ebc.uu.seORCID Iconhttps://orcid.org/0000-0002-7389-8849;4. Public Health Sciences, Karlstad University, Karlstad, Sweden;5. Icahn School of Medicine at Mount Sinai, New York, NY, USA;6. Department of Environmental Medicine and Public Health, Centre for Reproductive Biology in Uppsala (CRU), Uppsala, SwedenORCID Iconhttps://orcid.org/0000-0001-7664-7562;7. Department of Environmental Medicine and Public Health, Centre for Reproductive Biology in Uppsala (CRU), Uppsala, SwedenORCID Iconhttps://orcid.org/0000-0002-5328-6255
Abstract:ABSTRACT

Bisphenol A (BPA) and phthalate diesters are ubiquitous environmental contaminants. While these compounds have been reported as reproductive toxicants, their effects may partially be attributed to metabolites. The aim of this study was to examine reproductive organ development in chicken embryos exposed to the BPA metabolite, 4-methyl-2,4-bis(4-hydroxyphenyl)pent-1-ene (MBP; 100 µg/g egg) or a human-relevant mixture of 4 phthalate monoesters (85 µg/g egg). The mixture was designed within the EU project EDC-MixRisk based upon a negative association with anogenital distance in boys at 21 months of age in a Swedish pregnancy cohort. Chicken embryos were exposed in ovo from an initial stage of gonad differentiation (embryonic day 4) and dissected two days prior to anticipated hatching (embryonic day 19). No discernible effects were noted on reproductive organs in embryos exposed to the mixture. MBP-treated males exhibited retention of Müllerian ducts and feminization of the left testicle, while MBP-administered females displayed a diminished the left ovary. In the left testicle of MBP-treated males, mRNA expression of female-associated genes was upregulated while the testicular marker gene SOX9 was downregulated, corroborating a feminizing effect by MBP. Our results demonstrate that MBP, but not the phthalate monoester mixture, disrupts both male and female reproductive organ development in an avian embryo model.
Keywords:Chicken embryo  feminization  mixture  phthalates  4-methyl-2  4-bis(4-hydroxyphenyl)pent-1-ene (MBP)
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