Hypothalamic-pituitary-ovarian axis perturbation in the basis of bisphenol A (BPA) reproductive toxicity in female zebrafish (Danio rerio)

Ecotoxicol Environ Saf. 2018 Jul 30:156:116-124. doi: 10.1016/j.ecoenv.2018.03.029. Epub 2018 Mar 14.

Abstract

Thousands of safety-related studies have been published on bisphenol A (BPA), an ubiquitous environmental pollutant with estrogenic activity and many other potential biological effects. In recent years, BPA exposure has been shown to cause anovulation and infertility through irreversible alteration of the hypothalamic-pituitary-gonadal axis in several organisms, including fish and mammals. Recently, the European Chemical Agency classified BPA as a "substance of very high concern" because of its endocrine-disrupting properties, which have serious effects on human health. Given the risk of exposure to BPA as a pollutant in the environment, food, and drinking water, the objective of our study was to assess the effects of this compound on the adeno-hypophysis by means of a histopathological and morphometric study of the gonadotroph cells. In addition, using quantitative real-time PCR (qRT-PCR) assays, we analyzed the changes in the expression of Cyp19b (an aromatase gene). Zebrafish were randomly distributed into five groups: a control group and 4 treated groups which were exposed to different BPA concentrations (1, 10, 100 and 1000 µg/L). The effects of the different doses on Cyp19b mRNA molecules followed a non-monotonic curve, with the 1 and 1000 µg/L doses causing dramatic decreases in the number of Cyp19b transcripts while the doses of 10 and 100 µg/L caused important increases. The consequences might be deregulation of gonadotropic hormones causing degeneration of gonadotropic cells, as observed in BPA treated animals. This is the first study in which the gonadotroph cells have been evaluated using histomorphological endpoints after BPA exposure in zebrafish.

Keywords: Adeno-hypophysis; Cyp19b; Endocrine-disrupting chemical; Fish; Gonadotroph cell.

MeSH terms

  • Animals
  • Aromatase / genetics
  • Aromatase / metabolism
  • Benzhydryl Compounds / toxicity*
  • Biomarkers / metabolism
  • Dose-Response Relationship, Drug
  • Endocrine Disruptors / toxicity
  • Endpoint Determination
  • Female
  • Gonadotrophs / cytology
  • Gonadotrophs / drug effects
  • Hypothalamus / drug effects*
  • Ovary / drug effects*
  • Phenols / toxicity*
  • Reproduction / drug effects*
  • Zebrafish / metabolism*
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism

Substances

  • Benzhydryl Compounds
  • Biomarkers
  • Endocrine Disruptors
  • Phenols
  • Zebrafish Proteins
  • Aromatase
  • Cyp19a1b protein, zebrafish
  • bisphenol A