Bisphenol S, a Bisphenol A alternative, impairs swine ovarian and adipose cell functions

被引:49
作者
Berni, M. [1 ]
Gigante, P. [1 ]
Bussolati, S. [1 ]
Grasselli, E. [1 ]
Grolli, S. [1 ]
Ramoni, R. [1 ]
Basini, G. [1 ]
机构
[1] Univ Parma, Dipartimento Sci Med Vet, Via Taglio 10, I-43126 Parma, Italy
关键词
Granulosa cells; Steroidogenesis; Cell proliferation; Free radicals; Adipocyte; ENDOCRINE DISRUPTING COMPOUNDS; STEROID-HORMONE PRODUCTION; GRANULOSA-CELLS; ADIPOGENIC DIFFERENTIATION; ENVIRONMENTAL CHEMICALS; FEMALE INFERTILITY; ENDOTHELIAL-CELLS; HUMAN EXPOSURE; STEROIDOGENESIS; EXPRESSION;
D O I
10.1016/j.domaniend.2018.08.001
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The high-volume-produced plastic monomer Bisphenol A (BPA) has been in the spotlight in the last years because of its endocrine disruptor (ED) behavior, leading to disclosure of the association between the widespread human and wildlife exposure to BPA and reproductive, metabolic, and developmental disorders and hormone-dependent cancer onset. These evidences caused restrictions and prohibitions of BPA industrial uses and prompted investigation of harmless alternative compounds. Above all, several countries have substituted the parental analogue with Bisphenol S (BPS) in baby care product manufacturing, even if its structural homology to BPA suggests similar ED properties not yet completely ruled out. In light of this consideration, the aim of this in vitro study was to investigate the effect of BPS exposure (0.1, 1, and 10 mu M for 48 h) on granulosa cells that are considered the prime ovarian targets of BPA as a "reproductive toxicant". Our data document that BPS inhibited E2 production, cell proliferation, and scavenging nonenzymatic activity (P < 0.05) while it significantly (P < 0.05) stimulated cell viability, superoxide (O-2(-)) and nitric oxide (NO) production in cultured swine granulosa cells, a previously validated endocrine cell model for BPA. Evidence also exists that BPA and its analogues, as environmental lipophilic pollutants, are involved in the disruption of adipose tissue (AT) endocrine function, resulting in metabolic effects and thus in potential reproductive disorders. On this basis, our second purpose was the assessment of BPS effects on mesenchymal stromal cells (MSCs) isolated from porcine AT, taking into account MSCs viability and adipogenic differentiation, a process actually demonstrated to be largely affected by EDs. Our results show that BPS decreased (P < 0.001) cell viability of proliferating adipose stromal cells. Taken as a whole, our data demonstrate an effective BPS ED activity at mu M concentrations, suggesting that further studies are needed before considering its use in industrial application as an alternative to BPA. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:48 / 56
页数:9
相关论文
共 50 条
  • [21] Low doses of bisphenol F and S affect human ovarian granulosa cells by reducing the number of active mitochondria and ATP synthesis
    Glod, Paulina
    Marynowicz, Weronika
    Homa, Joanna
    Smoleniec, Joanna
    Maduzia, Dawid
    Ptak, Anna
    TOXICOLOGY LETTERS, 2025, 405 : 41 - 50
  • [22] Embryonic Exposure to Bisphenol A Impairs Primordial Germ Cell Migration without Jeopardizing Male Breeding Capacity
    Lombo, Marta
    Getino-Alvarez, Lidia
    Depince, Alexandra
    Labbe, Catherine
    Paz Herraez, Maria
    BIOMOLECULES, 2019, 9 (08)
  • [23] Bisphenol A induces ovarian cancer cell proliferation and metastasis through estrogen receptor-α pathways
    Sang, Chen
    Song, Yu
    Jin, Tong-wang
    Zhang, Shuo
    Fu, Linyan
    Zhao, Yi
    Zou, Xinxin
    Wang, Zhe
    Gao, Hui
    Liu, Sijin
    ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2021, 28 (27) : 36060 - 36068
  • [24] Bisphenol A induces ovarian cancer cell proliferation and metastasis through estrogen receptor-α pathways
    Chen Sang
    Yu Song
    Tong-wang Jin
    Shuo Zhang
    Linyan Fu
    Yi Zhao
    Xinxin Zou
    Zhe Wang
    Hui Gao
    Sijin Liu
    Environmental Science and Pollution Research, 2021, 28 : 36060 - 36068
  • [25] Preconceptional exposure of adult male rats to bisphenol S impairs insulin sensitivity and glucose tolerance in their male offspring
    Gong, Pengfei
    Bailbe, Danielle
    Tolu, Stefania
    Pommier, Gaelle
    Liu, Junjun
    Movassat, Jamileh
    CHEMOSPHERE, 2023, 314
  • [26] Prenatal Exposure to Bisphenol A, E, and S Induces Transgenerational Effects on Male Reproductive Functions in Mice
    Shi, Mingxin
    Whorton, Allison E.
    Sekulovski, Nikola
    MacLean, James A., II
    Hayashi, Kanako
    TOXICOLOGICAL SCIENCES, 2019, 172 (02) : 303 - 315
  • [27] Laccase Treatment Impairs Bisphenol A-Induced Cancer Cell Proliferation Affecting Estrogen Receptor α-Dependent Rapid Signals
    Bolli, Alessandro
    Galluzzo, Paola
    Ascenzi, Paolo
    Del Pozzo, Giovanna
    Manco, Immacolata
    Vietri, Maria Teresa
    Mita, Luigi
    Altucci, Lucia
    Mita, Damiano Gustavo
    Marino, Maria
    IUBMB LIFE, 2008, 60 (12) : 843 - 852
  • [28] Bisphenol S stimulates Leydig cell proliferation but inhibits differentiation in pubertal male rats through multiple mechanisms
    Pan, Peipei
    Wen, Zina
    Ma, Feifei
    Lei, Zhen
    Pan, Chengshuang
    Fei, Qianjin
    Tian, Erpo
    Wang, Yiyan
    Zhu, Qiqi
    Li, Huitao
    Li, Xiaoheng
    Zhong, Ying
    Ge, Ren-Shan
    Xu, Ren-ai
    ENVIRONMENTAL TOXICOLOGY, 2023, 38 (10) : 2361 - 2376
  • [29] High-Content Image-Based Single-Cell Phenotypic Analysis for the Testicular Toxicity Prediction Induced by Bisphenol A and Its Analogs Bisphenol S, Bisphenol AF, and Tetrabromobisphenol A in a Three-Dimensional Testicular Cell Co-culture Model
    Yin, Lei
    Siracusa, Jacob Steven
    Measel, Emily
    Guan, Xueling
    Edenfield, Clayton
    Liang, Shenxuan
    Yu, Xiaozhong
    TOXICOLOGICAL SCIENCES, 2020, 173 (02) : 313 - 335
  • [30] Low concentrations of bisphenol A promote human ovarian cancer cell proliferation and glycolysis-based metabolism through the estrogen receptor-α pathway
    Shi, Xiao-Yu
    Wang, Zhe
    Liu, Liyu
    Feng, Li-Min
    Li, Nan
    Liu, Sijin
    Gao, Hui
    CHEMOSPHERE, 2017, 185 : 361 - 367