Adverse Outcome Pathway Network–Based Assessment of the Interactive Effects of an Androgen Receptor Agonist and an Aromatase Inhibitor on Fish Endocrine Function. (21st February 2020)

• Record Type: Journal Article
• Authors: Ankley, Gerald T.; Blackwell, Brett R.; Cavallin, Jenna E.; Doering, Jon A.; Feifarek, David J.; Jensen, Kathleen M.; Kahl, Michael D.; LaLone, Carlie A.; Poole, Shane T.; Randolph, Eric C.; Saari, Travis W.; Villeneuve, Daniel L.
• Is Part Of: Environmental toxicology and chemistry. Volume 39:Number 4(2020)
• Page Start: 913
• Page End: 922
• Publication Date: 2020-02-21
• Subjects: Fish -- Endocrine -- Toxicity -- Mechanism -- Adverse outcome pathway; Pollution -- Environmental aspects -- Periodicals; Environmental chemistry -- Periodicals; 615.902
• DOI: 10.1002/etc.4668
• Languages: English
• ISSNs: 0730-7268

Abstract

Abstract: Predictive approaches to assessing the toxicity of contaminant mixtures have been largely limited to chemicals that exert effects through the same biological molecular initiating event. However, by understanding specific pathways through which chemicals exert effects, it may be possible to identify shared "downstream" nodes as the basis for forecasting interactive effects of chemicals with different molecular initiating events. Adverse outcome pathway (AOP) networks conceptually support this type of analysis. We assessed the utility of a simple AOP network for predicting the effects of mixtures of an aromatase inhibitor (fadrozole) and an androgen receptor agonist (17β‐trenbolone) on aspects of reproductive endocrine function in female fathead minnows. The fish were exposed to multiple concentrations of fadrozole and 17β‐trenbolone individually or in combination for 48 or 96 h. Effects on 2 shared nodes in the AOP network, plasma 17β‐estradiol (E2) concentration and vitellogenin (VTG) production (measured as hepatic vtg transcripts) responded as anticipated to fadrozole alone but were minimally impacted by 17β‐trenbolone alone. Overall, there were indications that 17β‐trenbolone enhanced decreases in E2 and vtg in fadrozole‐exposed fish, as anticipated, but the results often were not statistically significant. Failure to consistently observe hypothesized interactions between fadrozole and 17β‐trenbolone could be due to several factors, including lack of impact of 17β‐trenbolone, inherent biological variability in the endpoints assessed, and/or an incomplete understanding of interactions (including feedback) between different pathways within the hypothalamic–pituitary–gonadal axis. Environ Toxicol Chem 2020;39:913–922. © 2020 SETAC