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Title: Is bisphenol S a safe substitute for bisphenol A in terms of metabolic function? An in vitro study

As bisphenol A (BPA) has been shown to induce adverse effects on human health, especially through the activation of endocrine pathways, it is about to be withdrawn from the European market and replaced by analogues such as bisphenol S (BPS). However, toxicological data on BPS is scarce, and so it is necessary to evaluate the possible effects of this compound on human health. We compared the effect of BPA and BPS on obesity and hepatic steatosis processes using low doses in the same range as those found in the environment. Two in vitro models were used, the adipose cell line 3T3-L1 and HepG2 cells, representative of hepatic functions. We analyzed different parameters such as lipid and glucose uptakes, lipolysis, leptin production and the modulation of genes involved in lipid metabolism and energy balance. BPA and BPS induced an increase in the lipid content in the 3T3-L1 cell line and more moderately in the hepatic cells. We also observed a decrease in lipolysis after bisphenol treatment of adipocytes, but only BPS was involved in the increase in glucose uptake and leptin production. These latter effects could be linked to the modulation of SREBP-1c, PPARγ, aP2 and ERRα and γ genes aftermore » exposure to BPA, whereas BPS seems to target the PGC1α and the ERRγ genes. The findings suggest that both BPA and BPS could be involved in obesity and steatosis processes, but through two different metabolic pathways. - Highlights: • The non-monotonic effects of BPA and BPS act through 2 different metabolic pathways. • BPA and BPS induce an increase in the lipid content in adipocytes and hepatic cells. • BPS increased leptin production and glucose uptake in adipocyte and hepatocyte. • BPA and BPS could participate in metabolic deregulations leading to obesity or NAFLD.« less
Authors:
 [1] ;  [2] ;  [3] ;  [1] ;  [2] ;  [4] ;  [3]
  1. INRA, TOXALIM, 180 chemin de Tournefeuille, 31027 Toulouse (France)
  2. (France)
  3. INRA, UMR 1331 TOXALIM, 400 route des Chappes, BP 167, 06903 Sophia-Antipolis (France)
  4. Nutox Laboratory, Derttech “Packtox”, INSERM UMR 866, AgroSup Dijon, 1 esplanade Erasme, 21000 Dijon (France)
Publication Date:
OSTI Identifier:
22439869
Resource Type:
Journal Article
Resource Relation:
Journal Name: Toxicology and Applied Pharmacology; Journal Volume: 280; Journal Issue: 2; Other Information: Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; BIOLOGICAL PATHWAYS; DOSES; ENVIRONMENT; GENES; GLUCOSE; IN VITRO; LEPTIN; LIPIDS; LIVER; METABOLIC DISEASES; METABOLISM; PUBLIC HEALTH; UPTAKE