PUBLICATION

Thyroid disrupting effects of halogenated and next generation chemicals on the swim bladder development of zebrafish

Authors
Godfrey, A., Hooser, B., Abdelmoneim, A., Horzmann, K.A., Freeman, J.L., SepĂșlveda, M.S.
ID
ZDB-PUB-171105-2
Date
2017
Source
Aquatic toxicology (Amsterdam, Netherlands)   193: 228-235 (Journal)
Registered Authors
Keywords
Fish, Flame retardants, Perfluorinated, Surfactants, Swim bladder
MeSH Terms
  • Air Sacs/drug effects
  • Air Sacs/embryology
  • Animals
  • Caprylates/toxicity
  • Embryo, Nonmammalian/drug effects
  • Embryo, Nonmammalian/physiology
  • Endocrine Disruptors/toxicity*
  • Fluorocarbons/toxicity
  • Halogenation
  • Organophosphorus Compounds/toxicity
  • Phenanthrenes/toxicity
  • Polybrominated Biphenyls/toxicity
  • Thyroid Gland/drug effects
  • Thyroid Gland/embryology
  • Water Pollutants, Chemical/toxicity*
  • Zebrafish/embryology*
  • Zebrafish/metabolism
PubMed
29101780 Full text @ Aquat. Toxicol.
Abstract
Endocrine disrupting chemicals (EDCs) can alter thyroid function and adversely affect growth and development. Halogenated compounds, such as perfluorinated chemicals commonly used in food packaging, and brominated flame retardants used in a broad range of products from clothing to electronics, can act as thyroid disruptors. Due to the adverse effects of these compounds, there is a need for the development of safer next generation chemicals. The objective of this study was to test the thyroid disruption potential of old use and next generation halogenated chemicals. Zebrafish embryos were exposed to three old use compounds, perfluorooctanoic acid (PFOA), tetrabromobisphenol A (TBBPA) and tris (1,3-dichloro-2-propyl) phosphate (TDCPP) and two next generation chemicals, 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxdie (DOPO) and perfluorobutyric acid (PFBA). Sub-chronic (0-6days post fertilization (dpf)) and chronic (0-28dpf) exposures were conducted at 1% of the concentration known to kill 50% (LC50) of the population. Changes in the surface area of the swim bladder as well as in expression levels of genes involved in the thyroid control of swim bladder inflation were measured. At 6dpf, zebrafish exposed to all halogenated chemicals, both old use and next generation, had smaller posterior swim bladder and increased expression in the gene encoding thyroid peroxidase, tpo and the genes encoding two swim bladder surfactant proteins, sp-a and sp-c. These results mirrored the effects of thyroid hormone-exposed positive controls. Fish exposed to a TPO inhibitor (methimazole, MMI) had a decrease in tpo expression levels at 28dpf. Effects on the anterior swim bladder at 28dpf, after exposure to MMI as well as both old and new halogenated chemicals, were the same, i.e., absence of SB in ∼50% of fish, which were also of smaller body size. Overall, our results suggest thyroid disruption by the halogenated compounds tested via the swim bladder surfactant system. However, with the exception of TBBPA and TDCPP, the concentrations tested (∼5-137ppm) are not likely to be found in the environment.
Errata / Notes
This article is corrected by ZDB-PUB-211101-1.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping