Low doses of carbendazim and chlorothalonil synergized to impair mouse spermatogenesis through epigenetic pathways

Ecotoxicol Environ Saf. 2020 Jan 30:188:109908. doi: 10.1016/j.ecoenv.2019.109908. Epub 2019 Nov 6.

Abstract

Pesticides have been extensively produced and used to help the agricultural production which leads to the contamination of the environment, soil, groundwater sources, and even foodstuffs. Fungicides carbendazim (CBZ) and chlorothalonil (Chl) are widely applied in agriculture and other aspects. CBZ or Chl have been reported to disrupt spermatogenesis and decrease semen quality. However, it is not understood the effects of pubertal exposure to low doses of CBZ and Chl together, and the underlying mechanisms. Therefore, the aim of current investigation was to explore the negative impacts of pubertal exposure to low doses of CBZ and Chl together on spermatogenesis and the role of epigenetic modifications in the process. We demonstrated that CBZ and Chl together synergize to decrease sperm motility in vitro (CBZ 1.0 + Chl 0.1, CBZ 10.0 + CHl 1.0, CBZ 100.0 + Chl 10 μM in incubation medium for 24 h) and sperm concentration and motility in vivo with ICR mice (CBZ 0.1 + Chl 0.1, CBZ 1.0 + CHl 1.0, CBZ 10.0 + Chl 10 mg/kg body weight; oral gavage for five weeks). CBZ + Chl significantly increase reactive oxygen species (ROS) and apoptosis by the increase in the protein level of caspase 8 in vitro. Moreover, CBZ + Chl synergized to disrupt mouse spermatogenesis with the disturbance in sperm production proteins and sperm proteins (VASA, A-Myb, STK31, AR, Acrosin). CBZ + Chl synergized to decrease the protein level of estrogen receptor alpha and the protein level of DNA methylation marker 5 mC in Leydig cells, and to increase the protein levels of histone methylation marker H3K9 and the methylation enzyme G9a in germ cells. Therefore, greater attention should be paid to the use of CBZ and Chl as pesticides to minimise their adverse impacts on spermatogenesis.

Keywords: Carbendazim; Chlorothalonil; Epigenetic signalling pathways; Spermatogenesis.

MeSH terms

  • Animals
  • Benzimidazoles / toxicity*
  • Carbamates / toxicity*
  • Drug Synergism
  • Epigenesis, Genetic / drug effects*
  • Estrogen Receptor alpha / metabolism
  • Fungicides, Industrial / toxicity*
  • Male
  • Methylation / drug effects
  • Mice
  • Mice, Inbred ICR
  • Nitriles / toxicity*
  • Signal Transduction / drug effects
  • Spermatogenesis / drug effects*
  • Spermatogenesis / genetics
  • Spermatozoa / drug effects

Substances

  • Benzimidazoles
  • Carbamates
  • Estrogen Receptor alpha
  • Fungicides, Industrial
  • Nitriles
  • carbendazim
  • tetrachloroisophthalonitrile