Bisphenol F has different effects on preadipocytes differentiation and weight gain in adult mice as compared with Bisphenol A and S

被引:35
作者
Drobna, Zuzana [1 ,2 ]
Talarovicova, Alzbeta [1 ,2 ]
Schrader, Hannah E. [1 ,2 ]
Fennell, Timothy R. [1 ,2 ,3 ]
Snyder, Rodney W. [1 ,2 ,3 ]
Rissman, Emilie F. [1 ,2 ]
机构
[1] North Carolina State Univ, Ctr Human Hlth & Environm, Raleigh, NC 27695 USA
[2] North Carolina State Univ, Dept Biol Sci, Raleigh, NC 27695 USA
[3] RTI Int, Discovery Sci, Res Triangle Pk, NC 27709 USA
关键词
Bisphenol; Metabolism; Fat; BPF; Alternatives to BPA; Diabetes; 3T3-L1; CELLS; EXPOSURE; ANALOGS; ALTERNATIVES; HEALTH; TOXICITY; PROTOCOL; PARABENS; URINARY; CHINA;
D O I
10.1016/j.tox.2019.03.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bisphenol S (2,2-bisulfone, BPS) and Bisphenol F (2,2-bis [4-hydroxyphenol]methane, BPF) are analogs of Bisphenol A (2,2-bis[4-hydroxyphenyl]propane, BPA), a widely used endocrine disrupting compound present in polycarbonate plastics, thermal receipts and epoxy resins that line food cans. Here we examined effects of BPA, BPS, and BPF in low concentrations on differentiation in murine 3T3-L1 preadipocytes. We also fed adult male mice chow with one of three doses of BPF (0, 0.5, 5, 50 mg/kg chow, or approximately 0.044, 0.44 and 4.4 mg/kg body weight per day) for 12 weeks, collected body weights, food intake, and tested for glucose tolerance. The doses of BPF used produced mean concentrations of 0, 6.2, 43.6, and 561 ng/mL in plasma. In 3T3-L1 cells BPS had the greatest effects, along with BPA, both increased expression of several genes required for preadipocyte differentiation over 12 days in culture. In contrast, BPF decreased expression of several genes late in differentiation. This dichotomy was also reflected in lipid accumulation as BPA and BPS treated cells had elevated lipid concentrations compared to controls or cells treated with BPF. Male mice fed either the highest or lowest concentrations of BPF gained less weight than controls with no effects on glucose levels or glucose tolerance. Plasma levels of BPF reflected doses in food with no overlap between doses. In summary, our results suggest that BPS has a strong potential to be obesogenic while effects of BPF are subtler and potentially in the opposite direction.
引用
收藏
页码:66 / 72
页数:7
相关论文
共 43 条
[1]   Bisphenol S- and bisphenol A-induced adipogenesis of murine preadipocytes occurs through direct peroxisome proliferator-activated receptor gamma activation [J].
Ahmed, S. ;
Atlas, E. .
INTERNATIONAL JOURNAL OF OBESITY, 2016, 40 (10) :1566-1573
[2]   Biomonitoring of human exposures to chlorinated derivatives and structural analogs of bisphenol A [J].
Andra, Syam S. ;
Charisiadis, Pantelis ;
Arora, Manish ;
van Vliet-Ostaptchouk, Jana V. ;
Makris, Konstantinos C. .
ENVIRONMENT INTERNATIONAL, 2015, 85 :352-379
[3]   Migration of Parabens, Bisphenols, Benzophenone-Type UV Filters, Triclosan, and Triclocarban from Teethers and Its Implications for Infant Exposure [J].
Asimakopoulos, Alexandros G. ;
Elangovan, Madhavan ;
Kannan, Kurunthachalam .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2016, 50 (24) :13539-13547
[4]   NTP-CERHR expert panel report on the reproductive and developmental toxicity of bisphenol A [J].
Chapin, Robert E. ;
Adams, Jane ;
Boekelheide, Kim ;
Gray, L. Earl, Jr. ;
Hayward, Simon W. ;
Lees, Peter S. J. ;
McIntyre, Barry S. ;
Portier, Kenneth M. ;
Schnorr, Teresa M. ;
Selevan, Sherry G. ;
Vandenbergh, John G. ;
Woskie, Susan R. .
BIRTH DEFECTS RESEARCH PART B-DEVELOPMENTAL AND REPRODUCTIVE TOXICOLOGY, 2008, 83 (03) :157-395
[5]   Determination of bisphenol A and related substitutes/analogues in human breast milk using gas chromatography-tandem mass spectrometry [J].
Deceuninck, Yoann ;
Bichon, Emmanuelle ;
Marchand, Philippe ;
Boquien, Clair-Yves ;
Legrand, Arnaud ;
Boscher, Cecile ;
Antignac, Jean Philippe ;
Le Bizec, Bruno .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2015, 407 (09) :2485-2497
[6]   Obesogen effects after perinatal exposure of 4,4′-sulfonyldiphenol (Bisphenol S) in C57BL/6 mice [J].
Del Moral, L. Ivry ;
Le Corre, L. ;
Poirier, H. ;
Niot, I. ;
Truntzer, T. ;
Merlin, J. -F. ;
Rouimi, P. ;
Besnard, P. ;
Rahmani, R. ;
Chagnon, M. C. .
TOXICOLOGY, 2016, 357 :11-20
[7]   A new chapter in the bisphenol A story: bisphenol S and bisphenol F are not safe alternatives to this compound [J].
Eladak, Soria ;
Grisin, Tiphany ;
Moison, Delphine ;
Guerquin, Marie-Justine ;
N'Tumba-Byn, Thierry ;
Pozzi-Gaudin, Stephanie ;
Benachi, Alexandra ;
Livera, Gabriel ;
Rouiller-Fabre, Virginie ;
Habert, Rene .
FERTILITY AND STERILITY, 2015, 103 (01) :11-21
[8]   Effect of Perinatal Bisphenol A Exposure on Serum Lipids and Lipid Enzymes in Offspring Rats of Different Sex [J].
Gao Liang ;
Wang Han Ning ;
Zhang Ling ;
Peng Fang Yuan ;
Jia Yue ;
Wei Wei ;
Jia Li Hong .
BIOMEDICAL AND ENVIRONMENTAL SCIENCES, 2016, 29 (09) :686-+
[9]   Is bisphenol S a safe substitute for bisphenol A in terms of metabolic function? An in vitro study [J].
Helies-Toussaint, Cecile ;
Peyre, Ludovic ;
Costanzo, Claudia ;
Chagnon, Marie-Christine ;
Rahmani, Roger .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2014, 280 (02) :224-235
[10]   Subacute oral toxicity study of bisphenol F based on the draft protocol for the "Enhanced OECD Test Guideline no. 407" [J].
Higashihara, Nobuhiko ;
Shiraishi, Keiji ;
Miyata, Katusi ;
Oshima, Yutaka ;
Minobe, Yasushi ;
Yamasaki, Kanji .
ARCHIVES OF TOXICOLOGY, 2007, 81 (12) :825-832