Toxicity and multigenerational effects of bisphenol S exposure to Caenorhabditis elegans on developmental, biochemical, reproductive and oxidative stress
Author(s) -
Xiang Xiao,
Xiaowei Zhang,
Caiqin Zhang,
Jie Li,
Yansheng Zhao,
Ying Zhu,
Jiayan Zhang,
Xinghua Zhou
Publication year - 2019
Publication title -
toxicology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.709
H-Index - 31
eISSN - 2045-4538
pISSN - 2045-452X
DOI - 10.1039/c9tx00055k
Subject(s) - caenorhabditis elegans , genotoxicity , antioxidant , oxidative stress , offspring , bisphenol a , endocrine disruptor , biology , bisphenol s , brood , reproduction , toxicology , zoology , endocrine system , toxicity , genetics , microbiology and biotechnology , endocrinology , medicine , chemistry , gene , biochemistry , pregnancy , hormone , organic chemistry , epoxy
Bisphenol A (BPA) is a typical endocrine disruptor. Bisphenol S (BPS) has been widely used as a substitute for various plastic materials due to the limited application of BPA. However, it does not mean that BPS is a safe substitute due to the lack of effective evaluation of BPS. In this study, the clinical model of Caenorhabditis elegans (C. elegans) was used to study the effects of BPS on the locomotion behavior, growth, reproduction, lifespan and antioxidant system. Our study found that C. elegans exposed to 0.01 μM BPS could have significantly inhibited locomotion behavior and growth, as well as damaged reproductive and antioxidant systems and lifespan. It is interesting to note that in multi-generational exposure studies, we found that BPS exhibits complex genotoxicity. With the transmission to the offspring, BPS showed more significant inhibition of the head thrashes of the nematode, while the effect on the body bends and body length was gradually weakened. The effect of BPS on the brood size shows different rules according to different concentrations and offsprings. Therefore, the safety of BPS still needs further evaluation, especially the multi-generational genotoxicity.
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