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Cytogenetic and developmental toxicity of bisphenol A and bisphenol S in Arbacia lixula sea urchin embryos

Ecotoxicology 2022 9 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 45 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Raja Rezg, Raja Rezg, Giovanni Pagano, Marco Trifuoggi Rahime Oral, Rahime Oral, Giovanni Pagano, Rahime Oral, Serkan Tez, Serkan Tez, Marco Trifuoggi Marco Trifuoggi Marco Trifuoggi Rahime Oral, Giovanni Pagano, Bessem Mornagui, Marco Trifuoggi Giovanni Pagano, Bessem Mornagui, Marco Trifuoggi Serkan Tez, Serkan Tez, Serkan Tez, Giovanni Pagano, Marco Trifuoggi Marco Trifuoggi Marco Trifuoggi Rahime Oral, Rahime Oral, Rahime Oral, Giovanni Pagano, Marco Trifuoggi Marco Trifuoggi Marco Trifuoggi Marco Trifuoggi Marco Trifuoggi Marco Trifuoggi

Summary

Both bisphenol A and bisphenol S caused dose-dependent embryotoxicity and developmental abnormalities in sea urchin (Arbacia lixula) embryos at concentrations starting from 1 micromolar, with BPS showing similar or greater toxicity than BPA in several endpoints. The findings challenge the assumption that BPS is a safer alternative to BPA for marine ecosystems.

Body Systems

Bisphenol S (BP-S) is one of the most important substitutes of bisphenol A (BP-A), and its environmental occurrence is predicted to intensify in the future. Both BP-A and BP-S were tested for adverse effects on early life stages of Arbacia lixula sea urchins at 0.1 up to 100 µM test concentrations, by evaluating cytogenetic and developmental toxicity endpoints. Embryonic malformations and/or mortality were scored to determine embryotoxicity (72 h post-fertilization). It has been reported in academic dataset that bisphenols concentration reached μg/L in aquatic environment of heavily polluted areas. We have chosen concentrations ranging from 0.1-100 μM in order to highlight, in particular, BP-S effects. Attention should be paid to this range of concentrations in the context of the evaluation of the toxicity and the ecological risk of BP-S as emerging pollutant. Cytogenetic toxicity was measured, using mitotic activity and chromosome aberrations score in embryos (6 h post-fertilization). Both BP-A and BP-S exposures induced embryotoxic effects from 2.5 to 100 µM test concentrations as compared to controls. Malformed embryo percentages following BP-A exposure were significantly higher than in BP-S-exposed embryos from 0.25 to 100 µM (with a ~5-fold difference). BP-A, not BP-S exhibited cytogenetic toxicity at 25 and 100 µM. Our results indicate an embryotoxic potential of bisphenols during critical periods of development with a potent rank order to BP-A vs. BP-S. Thus, we show that BP-A alternative induce similar toxic effects to BP-A with lower severity.

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