4.8 Article

Development of a Comprehensive Toxicity Pathway Model for 17α-Ethinylestradiol in Early Life Stage Fathead Minnows (Pimephales promelas)

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 55, 期 8, 页码 5024-5036

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.0c05942

关键词

fathead minnow; transcriptomics; proteomics; histology; estrogen; toxicity pathway

资金

  1. Genome Canada
  2. Genome Quebec
  3. Genome Prairies
  4. Government of Canada
  5. University of Saskatchewan
  6. McGill University
  7. US Environmental Protection Agency
  8. US Army Corps of Engineers
  9. Qiagen
  10. SGS AXYS
  11. Shell USA
  12. CEITEC 2020 [LQ1601]
  13. CIISB research infrastructure project - MEYS CR [LM2018127]
  14. project eInfrastruktura CZ [e-INFRA LM2018140]
  15. CRC Program of NSERC
  16. University of Saskatchewan Dean's Scholarship
  17. Toxicology Devolved Scholarship
  18. Mitacs Globalink Research Award
  19. NSERC-PGSD3 [504753-2017]
  20. NSERC
  21. ECCC
  22. Ministere de l'Economie, de la Science et de l'Innovation du Quebec

向作者/读者索取更多资源

This study aimed to develop a comprehensive early life stage toxicity pathway model for fish exposed to estrogenic chemicals, rooted in mechanistic toxicology. The integration of omics data improved the interpretation of perturbations in early life stage fish, showing promise as a replacement for standard adult live animal tests. The study provided evidence of conservation of toxicity pathways across levels of biological organization.
There is increasing pressure to develop alternative ecotoxicological risk assessment approaches that do not rely on expensive, time-consuming, and ethically questionable live animal testing. This study aimed to develop a comprehensive early life stage toxicity pathway model for the exposure of fish to estrogenic chemicals that is rooted in mechanistic toxicology. Embryo-larval fathead minnows (FHM; Pimephales promelas) were exposed to graded concentrations of 17 alpha-ethinylestradiol (water control, 0.01% DMSO, 4, 20, and 100 ng/L) for 32 days. Fish were assessed for transcriptomic and proteomic responses at 4 days post-hatch (dph), and for histological and apical end points at 28 dph. Molecular analyses revealed core responses that were indicative of observed apical outcomes, including biological processes resulting in overproduction of vitellogenin and impairment of visual development. Histological observations indicated accumulation of proteinaceous fluid in liver and kidney tissues, energy depletion, and delayed or suppressed gonad development. Additionally, fish in the 100 ng/L treatment group were smaller than controls. Integration of omics data improved the interpretation of perturbations in early life stage FHM, providing evidence of conservation of toxicity pathways across levels of biological organization. Overall, the mechanism-based embryo-larval FHM model showed promise as a replacement for standard adult live animal tests.

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