Developmental Exposure to Low Concentrations of Organophosphate Flame Retardants Causes Life-Long Behavioral

Lilah Glazer1, Andrew B Hawkey1, Corinne N Wells1

  • 1Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, North Carolina 27710.

Insights

Organophosphate flame retardants (OPFRs) may pose risks, as this study found they can cause lifelong neurobehavioral effects, including altered larval motility and adult anxiety, in zebrafish. These findings suggest OPFRs may not be safe alternatives to older flame retardants.

Area of Science:

  • Environmental toxicology
  • Neuroscience
  • Developmental toxicology

Background:

  • Older brominated flame retardants (BFRs) are being phased out due to neurotoxicity concerns.
  • Organophosphate flame retardants (OPFRs) are emerging as replacements, but their developmental neurotoxicity is largely unknown.

Purpose of the Study:

  • To investigate the lifelong neurobehavioral effects of four widely used OPFRs.
  • To assess the potential of OPFRs to cause developmental neurotoxicity and behavioral consequences.

Main Methods:

  • Zebrafish embryos were exposed to isopropylated phenyl phosphate (IPP), butylphenyl diphenyl phosphate (BPDP), 2-ethylhexyl diphenyl phosphate (EHDP), or isodecyl diphenyl phosphate (IDDP) from 0-5 days post-fertilization.
  • Larval motility was assessed on day 6.
  • Adult fish (5-7 months) underwent behavioral testing for emotional function, sensorimotor response, social interaction, and predator evasion.

Main Results:

  • All tested OPFRs caused chemical-specific alterations in larval motility.
  • Exposure to IPP, BPDP, or EHDP resulted in long-term impairment of anxiety-related behaviors in adult zebrafish.
  • IDDP exposure did not lead to significant long-term behavioral changes in adults.

Conclusions:

  • OPFRs may not be safe alternatives to BFRs, as they can induce significant neurobehavioral effects throughout the lifespan.
  • These findings highlight the need for further research into the risks of OPFRs in mammalian models and humans.

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