Oxidative stress and cytotoxicity induced by tetrachlorobisphenol A in Saccharomyces cerevisiae cells

Ecotoxicol Environ Saf. 2018 Oct:161:1-7. doi: 10.1016/j.ecoenv.2018.05.070. Epub 2018 May 29.

Abstract

Tetrachlorobisphenol A (TCBPA), which is widely used as flame retardant, can be released into various environments, thereby being absorbed by wildlife or human beings through food chain's bio-magnification and causing some adverse influences on wildlife or human beings. However, limited data are currently available on TCBPA-associated cytotoxicity and related mechanisms. Here, the cytotoxicity induced by different concentrations of TCBPA (i.e., 5, 10 and 20 μM) was studied using Saccharomyces cerevisiae, a simple eukaryotic model organism. TCBPA treatment inhibited the growth and survival rate of yeast cell in a dose-dependent manner. Moreover, TCBPA promoted the increasing of intracellular oxidative stress by enhancing accumulation of intracellular reactive oxygen species (ROS). Meanwhile, lipid peroxidation degree (represented by malondialdehyde (MDA) content) and DNA damage degree (represented by 8-hydroxy deoxyguanosine (8-oxodG) content) in yeast cell also increased after TCBPA treatment. However, yeast cell mitochondrial membrane potential (Δψm) decreased after TCBPA treatment. It was noteworthy that there was no significant inhibitory effect on yeast cell growth or survival rate in 5 μM TCBPA-treated cells, but the intracellular MDA content and Δψm level changed significantly, suggesting the potential cell damage secondary to the relative low dose of TCBPA exposure. Results presented here would highlight our knowledge about TCBPA-associated cytotoxicity in organisms.

Keywords: Cytotoxicity; Oxidative stress; Saccharomyces cerevisiae; Tetrachlorobisphenol A.

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Cell Count
  • Cell Cycle
  • Cell Proliferation
  • Chlorophenols / toxicity*
  • DNA Damage
  • Deoxyguanosine / analogs & derivatives
  • Deoxyguanosine / metabolism
  • Flame Retardants / toxicity*
  • Humans
  • Lipid Peroxidation / drug effects
  • Malondialdehyde / metabolism
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / drug effects
  • Oxidative Stress / drug effects*
  • Reactive Oxygen Species / metabolism
  • Saccharomyces cerevisiae / drug effects*
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / growth & development

Substances

  • Chlorophenols
  • Flame Retardants
  • Reactive Oxygen Species
  • Malondialdehyde
  • 8-Hydroxy-2'-Deoxyguanosine
  • tetrachlorodian
  • Deoxyguanosine