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

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

Environmental health perspectives (2009-05-15)
Daniel L Villeneuve, Nathaniel D Mueller, Dalma Martinović, Elizabeth A Makynen, Michael D Kahl, Kathleen M Jensen, Elizabeth J Durhan, Jenna E Cavallin, David Bencic, Gerald T Ankley
ZUSAMMENFASSUNG

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

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Sigma-Aldrich
3-Isobutyl-1-methylxanthin, BioUltra, ≥99%
Sigma-Aldrich
Medium 199, HEPES Modification, with Earle′s salts, L-glutamine and 25 mM HEPES, without sodium bicarbonate, powder, suitable for cell culture
Sigma-Aldrich
25-Hydroxycholesterin, ≥98%