4.7 Article

Effects of pyrethroid pesticide cis-bifenthrin on lipogenesis in hepatic cell line

Journal

CHEMOSPHERE
Volume 201, Issue -, Pages 840-849

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2018.03.009

Keywords

Pyrethroids; Lipid metabolism; cis-bifenthrin; Pregnane X receptor; Enantioselective

Funding

  1. National Science Foundation of China [21707120]
  2. Zhejiang Provincial Key Research and Development Program of China [2015C02019]
  3. National Key Research and Development Program of China [2016YFD0200804]

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Mounting evidence suggests there is a link between exposure to synthetic pyrethroids (SPs) and the development of obesity. The information presented in this study suggests that cis-bifenthrin (cis-BF) could activate pregnane X receptor (PXR) mediated pathway and lead to the lipid accumulation of human hepatoma (HepG2) cells. Cells were incubated in the control or different concentrations of cis-BF for 24 h. The 1 x 10(-7) M and 1 x 10(-6) M cis-BF exposure were found to induce cellular triglyceride (TG) accumulation significantly. This phenomenon was further supported by Oil Red O Staining assay. The cis-BF exposure caused upregulation of PXR gene and protein. Correspondingly, we also observed the increased expression of downstream genes involved in lipid formation and the inhibition of the expression of beta-oxidation. As chiral pesticide, cis-BF was further conformed to behave enantioselectivity in the lipid metabolism. Rather than 1R-cis-BF, HepG2 cells incubated with 1S-cis-BF exhibited a significant TG accumulation. 1S-cis-BF also showed a higher binding level, of which the KD value was 9.184 x 10(-8) M in the SPR assay, compared with 1R-cis-BF (3.463 x 10(-6) M). In addition, the molecular docking simulation analyses correlated well with the KD values measured by the SPR, indicating that 1S-cis-BF showed a better binding affinity with PXR. The results in this study also elucidates the differences between the two enantiomers of pyrethroid-induced toxicity in lipid metabolism of non-target organism. (C) 2018 Elsevier Ltd. All rights reserved.

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