4.6 Article

Exposure to alternative bisphenols BPS and BPF through breast milk: Noxious heritage effect during nursing associated with idiopathic infertility

期刊

TOXICOLOGY AND APPLIED PHARMACOLOGY
卷 413, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.taap.2021.115409

关键词

Bisphenol; Oocyte maturation; Spindle formation; Epigenetics

资金

  1. Czech Health Research Council [NV18-01-00544]
  2. Charles University Research Fund (Progress Q39)
  3. National Sustainability Programme I (NPU I) by the Ministry of Education, Youth and Sports of the Czech Republic (MEYS CR) [LO1503]
  4. MEYS CR [SVV 02690, CZ.02.1.01/0.0/0.0/16_019/0000787]
  5. European Regional Development Fund, European Human Biomonitoring Initiative
  6. H2020
  7. Czech Ministry of Agriculture [MZE-RO 0718]

向作者/读者索取更多资源

Research shows that BPA analogues BPS and BPF have deleterious effects on reproduction, potentially affecting the quality of offspring oocytes during breastfeeding. While the ovarian histology remains unaffected, there are alterations in spindle formation and epigenetic markers. The sensitivity of in-vitro matured oocytes to BPS and BPF is significantly noted, impacting developmental competence.
There is increasing evidence that bisphenols BPS and BPF, which are analogues of BPA, have deleterious effects on reproduction even at extremely low doses. Indirect exposure via the maternal route (i.e. across the placenta and/or by breastfeeding) is underestimated, although it can be assumed to be a cause of idiopathic female infertility. Therefore, we hypothesised the deleterious effects of exposure to BPA analogues during breastfeeding on the ovarian and oocyte quality of offspring. A 15-day exposure period of pups was designed, whilst nursing dams (N >= 6 per experimental group) were treated via drinking water with a low (0.2 ng/g body weight/day) or moderate (20 ng/g body weight/day) dose of bisphenol, mimicking real exposure in humans. Thereafter, female pups were bred to 60 days and oocytes were collected. Immature oocytes were used in the in-vitro maturation assay; alternatively, in-vivo-matured oocytes were isolated and used for parthenogenetic activation. Both in-vitro and in-vivo-matured oocytes were subjected to immunostaining of spindle microtubules (alpha-tubulin) and demethylation of histone H3 on the lysine K27 (H3K27me2) residue. Although very low doses of both BPS and BPF did not affect the quality of ovarian histology, spindle formation and epigenetic signs were affected. Notably, in-vitro matured oocytes were significantly sensitive to both doses of BPS and BPF. Although no significant differences in spindle-chromatin quality were identified in ovulated and in-vivo-matured oocytes, developmental competence was significantly damaged. Taken together, our mouse model provides evidence that bisphenol analogues represent a risk to human reproduction, possibly leading to idiopathic infertility in women.

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