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Bisphenol A exposure induces testicular oxidative damage via FTO/m6A/Nrf2 axis during postnatal development in mice

Ling, Yuanchao ; Huang, Xiaodi ; Li, Anlong ; Zhang, Jinzhi ; Chen, Jianmei ; Ren, Jiale ; Liu, Yanan ; Xie, Meina

Journal of applied toxicology, 2023-05, Vol.43 (5), p.694-705 [Periódico revisado por pares]

England: Wiley Subscription Services, Inc

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  • Título:
    Bisphenol A exposure induces testicular oxidative damage via FTO/m6A/Nrf2 axis during postnatal development in mice
  • Autor: Ling, Yuanchao ; Huang, Xiaodi ; Li, Anlong ; Zhang, Jinzhi ; Chen, Jianmei ; Ren, Jiale ; Liu, Yanan ; Xie, Meina
  • Assuntos: Alpha-Ketoglutarate-Dependent Dioxygenase FTO - metabolism ; Animals ; Antioxidants ; Antioxidants - metabolism ; Apoptosis ; Benzhydryl Compounds - toxicity ; Bisphenol A ; Epithelium ; Epoxy resins ; Exposure ; FTO ; m6A modification ; Male ; Males ; Mice ; N6-methyladenosine ; Neonates ; NF-E2-Related Factor 2 - genetics ; NF-E2-Related Factor 2 - metabolism ; Nrf2 ; Oxidative Stress ; Polycarbonate ; Polymerase chain reaction ; RNA modification ; Spermatogenesis ; Testes ; Testis ; Toxicity
  • É parte de: Journal of applied toxicology, 2023-05, Vol.43 (5), p.694-705
  • Descrição: Bisphenol A (BPA), a commonly used plasticizer in the production of polycarbonate plastics and epoxy resins, has been shown to induce male reproductive toxicity. However, the effects of BPA exposure on early testicular development have not been thoroughly studied, and the underlying mechanism is yet to be elucidated. In the current study, neonatal male mice were exposed to BPA at 0, 0.1, and 5 mg/kg, respectively, by daily subcutaneous injection during postnatal day (PND) 1–35 to explore its effects on testicular development at PND 36 (the end of the first round of spermatogenesis). Morphological analyses showed that BPA exposure significantly induced apoptosis of testicular cells (p < 0.01 and p < 0.001) and reduced the thickness of seminiferous epithelium (p < 0.01). In addition, BPA exposure significantly decreased the total antioxidant capacity of testes and levels of transcription factor Nrf2 as well as its downstream antioxidant molecules of NQO1 and GPx‐1 (p < 0.05 and p < 0.01). Furthermore, global m6A modifications of mRNAs were upregulated accompanied by declined m6A demethylase (FTO) in the testes of BPA groups (p < 0.05 and p < 0.01). MeRIP‐quantitative real‐time polymerase chain reaction (qPCR) demonstrated that BPA exposure markedly increased the m6A modification of Nrf2 mRNA (p < 0.05 and p < 0.01). These findings suggest that upregulation of m6A induced by inhibited FTO may be involved in BPA‐induced testicular oxidative stress and developmental injury during postnatal development, which provides a new idea to reveal the mechanism underlying BPA interfering with testicular development. Neonatal mice were exposed to BPA during the first round of spermatogenesis to explore its effects on testicular development. We found that BPA exposure induced testicular oxidative damage by downregulating testicular expression of Nrf2 and its downstream antioxidant molecules. Furthermore, BPA inhibited testicular FTO expression and elevated the total m6A RNA modifications in testes. The downregulation of Nrf2 protein induced by BPA may result from the elevated m6A modifications of Nrf2 mRNA.
  • Editor: England: Wiley Subscription Services, Inc
  • Idioma: Inglês
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  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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