AI Article Synopsis

  • Bisphenol A (BPA) has been banned in food products due to its endocrine-disrupting effects, leading to the rise of Bisphenol S (BPS) as an unregulated alternative in the plastic industry.
  • The study investigated the effects of various concentrations of BPS on ewe oocyte quality during in vitro maturation, finding significant decreases in cleavage and blastocyst rates at certain doses.
  • Results indicated that BPS negatively impacts reproductive competence in ewes and may not be a safe substitute for BPA, highlighting the need for more research on its mechanisms.

Article Abstract

Introduction: Bisphenol A (BPA) is a widespread compound in the plastic industry that is especially used to produce baby bottles, food packaging and metal cans. BPA, an endocrine disruptor, leads to alterations in reproductive function and therefore has been banned from the food industry. Unregulated BPA analogues, particularly Bisphenol S (BPS), have emerged and are now used in the plastic industry. Thus, this study aimed to examine the acute effects of low and environmental doses of BPS on ewe oocyte quality and developmental competence, and its mechanism of action, during in vitro maturation.

Methods: Ewe cumulus-oocyte complexes underwent in vitro maturation in the presence or absence of BPS (1 nM, 10 nM, 100 nM, 1 µM or 10 µM). Oocytes were then subjected to in vitro fertilisation and development.

Results: 1 µM BPS induced a 12.7% decrease in the cleavage rate ( = 0.004) and a 42.6% decrease in the blastocyst rate ( = 0.017) compared to control. The blastocyst rate reduction was also observed with 10 nM BPS. Furthermore, 10 µM BPS reduced the oocyte maturation rate, and 1 µM BPS decreased cumulus cell progesterone secretion. PR and AMH gene expression were reduced in cumulus cells. BPS induced a 5-fold increase in MAPK 3/1 activation ( = 0.04).

Conclusions: BPS impaired ewe oocyte developmental competence. The data suggest that BPS might not be a safe BPA analogue. Further studies are required to elucidate its detailed mechanism of action.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072985PMC
http://dx.doi.org/10.3390/ijms21041238DOI Listing

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