Direct effects, compensation, and recovery in female fathead minnows exposed to a model aromatase inhibitor

Environ Health Perspect. 2009 Apr;117(4):624-31. doi: 10.1289/ehp.11891. Epub 2008 Dec 12.

Abstract

Background: Several chemicals in the environment have the potential to inhibit aromatase, an enzyme critical to estrogen synthesis.

Objectives: The objective of this study was to provide a detailed characterization of molecular and biochemical responses of female fathead minnows to a model aromatase inhibitor, fadrozole (FAD).

Methods: Fish were exposed via water to 0, 3, or 30 microg FAD/L for 8 days and then held in clean water for 8 days, with samples collected at four time points during each 8-day period. We quantified ex vivo steroid production, plasma steroids, and plasma vitellogenin (Vtg) concentrations and analyzed relative transcript abundance of 10 key regulatory genes in ovaries and 3 in pituitary tissue by real-time polymerase chain reaction.

Results: Ex vivo 17beta-estradiol (E2) production and plasma E2 and Vtg concentrations were significantly reduced after a single day of exposure to 3 microg or 30 microg FAD/L. However, plasma E2 concentrations recovered by the eighth day of exposure in the 3-microg/L group and within 1 day of cessation of exposure in the 30-microg/L group, indicating concentration- and time-dependent physiologic compensation and recovery. Concentration-dependent increases in transcripts coding for aromatase (A isoform), cytochrome P450 side-chain cleavage, steroidogenic acute regulatory protein, and follicle-stimulating hormone receptor all coincided with increased E2 production and recovery of plasma E2 concentrations.

Conclusions: Results of this research highlight the need to consider compensation/adaptation and recovery when developing and interpreting short-term bioassays or biomarkers or when trying to predict the effects of chemical exposures based on mode of action.

Keywords: adaptation; endocrine disruption; estradiol; fadrozole; fish; gene expression; reproduction; steroid biosynthesis; vitellogenin.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Aromatase Inhibitors / analysis
  • Aromatase Inhibitors / toxicity*
  • Cyprinidae / genetics
  • Cyprinidae / metabolism*
  • Estradiol / analysis
  • Estradiol / blood
  • Fadrozole / analysis
  • Fadrozole / toxicity*
  • Female
  • Gene Expression Regulation / drug effects
  • Hormones / metabolism
  • RNA, Messenger / metabolism
  • Steroids / blood
  • Steroids / metabolism
  • Testosterone / analysis
  • Testosterone / blood
  • Toxicity Tests
  • Vitellogenins / blood
  • Vitellogenins / drug effects

Substances

  • Aromatase Inhibitors
  • Hormones
  • RNA, Messenger
  • Steroids
  • Vitellogenins
  • Testosterone
  • Estradiol
  • Fadrozole