First and Last Name/s of Presenters

Ryann HenryFollow
Reagan Vander Heide

Mentor/s

Dr. Nicole Roy

Participation Type

Poster

Abstract

Polybrominated diphenyl ethers (PBDEs) are added in high volumes to textiles, furniture foams, plastics and electronics as flame retardants. Although these PBDEs are effective in protecting property and human life from fire, their high production volumes have led PBDEs to be pervasive environmental contaminants and pose an ecological risk. Here we investigate the developmental neurotoxicity of 2,2’,4,4’-tetrabromodiphenyl ether (BDE-47) using the zebrafish vertebrate model system. We treated zebrafish embryos with control, vehicle, low (5µM) and high concentration (20µM) of BDE-47 at 6 hours post-fertilization before the onset of gastrulation and treated continuously until 6 days. Consistent with others, we find abnormal curvature of the body with flexion of the hindbrain, but studies on neurotoxicity were lacking. Using a transgenic expressing green fluorescent protein in the branchiomotor neurons of the hindbrain, we find a significant decrease in the length of rhombomere 1-8 and loss of the canonical patterning of branchiomotor neurons V-VII in treated embryos. We further investigated oligodendrocytes in the hindbrain using a myelin basic protein transgenic and found a significant decrease in the number of oligodendrocytes in the hindbrain of treated embryos. Given the abnormal curvature of the body, we also investigated muscle myofibrils and primary motor neurons which innervate the trunk musculature. We find that by 6 days, muscle myofibrils are disrupted in a concentration dependent manner, but despite the spinal curvature, the motor neuron pattern along the chevron-shaped somites was not affected. However, BDE-47 treated embryos demonstrated a decrease in motoneuron signal. Here we conclude that BDE-47 is neurotoxic to the developing embryos.

College and Major available

College of Arts and Sciences, Biology

Academic Level

Undergraduate student

Location

Digital Commons & West Campus West Building University Commons

Start Day/Time

4-25-2025 12:00 PM

End Day/Time

4-25-2025 2:00 PM

Students' Information

Ryann Henry, Biology Major, Chemistry and Dance Minor, Honors student, 2026

Honorable Mention, Most Scholarly Impact or Potential 2025 Award

Creative Commons License

Creative Commons Attribution-Noncommercial 4.0 License
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License

Prize Categories

Best Multidisciplinary Research or Collaboration, Most Scholarly Impact or Potential, Best Visuals

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Apr 25th, 12:00 PM Apr 25th, 2:00 PM

Neurotoxicity of 2,2’,4,4’-tetrabromodiphenyl ether (BDE-47) during embryonic zebrafish development.

Digital Commons & West Campus West Building University Commons

Polybrominated diphenyl ethers (PBDEs) are added in high volumes to textiles, furniture foams, plastics and electronics as flame retardants. Although these PBDEs are effective in protecting property and human life from fire, their high production volumes have led PBDEs to be pervasive environmental contaminants and pose an ecological risk. Here we investigate the developmental neurotoxicity of 2,2’,4,4’-tetrabromodiphenyl ether (BDE-47) using the zebrafish vertebrate model system. We treated zebrafish embryos with control, vehicle, low (5µM) and high concentration (20µM) of BDE-47 at 6 hours post-fertilization before the onset of gastrulation and treated continuously until 6 days. Consistent with others, we find abnormal curvature of the body with flexion of the hindbrain, but studies on neurotoxicity were lacking. Using a transgenic expressing green fluorescent protein in the branchiomotor neurons of the hindbrain, we find a significant decrease in the length of rhombomere 1-8 and loss of the canonical patterning of branchiomotor neurons V-VII in treated embryos. We further investigated oligodendrocytes in the hindbrain using a myelin basic protein transgenic and found a significant decrease in the number of oligodendrocytes in the hindbrain of treated embryos. Given the abnormal curvature of the body, we also investigated muscle myofibrils and primary motor neurons which innervate the trunk musculature. We find that by 6 days, muscle myofibrils are disrupted in a concentration dependent manner, but despite the spinal curvature, the motor neuron pattern along the chevron-shaped somites was not affected. However, BDE-47 treated embryos demonstrated a decrease in motoneuron signal. Here we conclude that BDE-47 is neurotoxic to the developing embryos.