Putative adverse outcome pathway development based on physiological responses of female fathead minnows to model estrogen versus androgen receptor agonists.


Journal

Aquatic toxicology (Amsterdam, Netherlands)
ISSN: 1879-1514
Titre abrégé: Aquat Toxicol
Pays: Netherlands
ID NLM: 8500246

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 06 04 2023
revised: 05 06 2023
accepted: 07 06 2023
medline: 8 8 2023
pubmed: 25 6 2023
entrez: 24 6 2023
Statut: ppublish

Résumé

Several adverse outcome pathways (AOPs) have linked molecular initiating events like aromatase inhibition, androgen receptor (AR) agonism, and estrogen receptor (ER) antagonism to reproductive impairment in adult fish. Estrogen receptor agonists can also cause adverse reproductive effects, however, the early key events (KEs) in an AOP leading to this are mostly unknown. The primary aim of this study was to develop hypotheses regarding the potential mechanisms through which exposure to ER agonists might lead to reproductive impairment in female fish. Mature fathead minnows were exposed to 1 or 10 ng 17α-ethynylestradiol (EE2)/L or 10 or 100 µg bisphenol A (BPA)/L for 14 d. The response to EE2 and BPA was contrasted with the effects of 500 ng/L of 17β-trenbolone (TRB), an AR agonist, as well as TRB combined with the low and high concentrations of EE2 or BPA tested individually. Exposure to 10 ng EE2/L, 100 µg BPA/L, TRB, or the various mixtures with TRB caused significant decreases in plasma concentrations of 17β-estradiol. Exposure to TRB alone caused a significant reduction in plasma vitellogenin (VTG), but VTG was unaffected or even increased in females exposed to EE2 or BPA alone or, in most cases, in mixtures with TRB. Over the course of the 14-d exposure, the only treatments that clearly did not affect egg production were 1 ng EE2/L and 10 µg BPA/L. Based on these results and knowledge of hypothalamic-pituitary-gonadal axis function, we hypothesize an AOP whereby decreased production of maturation-inducing steroid leading to impaired oocyte maturation and ovulation, possibly due to negative feedback or direct inhibitory effects of membrane ER activation, could be responsible for causing adverse reproductive impacts in female fish exposed to ER agonists.

Identifiants

pubmed: 37354817
pii: S0166-445X(23)00210-2
doi: 10.1016/j.aquatox.2023.106607
pii:
doi:

Substances chimiques

Androgens 0
Water Pollutants, Chemical 0
Estrogens 0
Ethinyl Estradiol 423D2T571U
Vitellogenins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106607

Informations de copyright

Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Mackenzie L Morshead (ML)

Oak Ridge Institute for Science and Education, US EPA, Great Lakes Toxicology and Ecology Division, Duluth, MN, USA.

Kathleen M Jensen (KM)

US EPA, Great Lakes Toxicology and Ecology Division, Duluth, MN, USA.

Gerald T Ankley (GT)

US EPA, Great Lakes Toxicology and Ecology Division, Duluth, MN, USA.

Sara Vliet (S)

US EPA, Scientific Computing and Data Curation Division, Duluth, MN, USA.

Carlie A LaLone (CA)

US EPA, Great Lakes Toxicology and Ecology Division, Duluth, MN, USA.

Alejandro Vidales Aller (AV)

Arizona State University, School of Mathematical and Natural Sciences, Phoenix, AZ, USA.

Karen H Watanabe (KH)

Arizona State University, School of Mathematical and Natural Sciences, Phoenix, AZ, USA.

Daniel L Villeneuve (DL)

US EPA, Great Lakes Toxicology and Ecology Division, Duluth, MN, USA. Electronic address: villeneuve.dan@epa.gov.

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Classifications MeSH