|ZFIN ID: ZDB-PUB-190925-1|
Exposure of Larval Zebrafish to the Insecticide Propoxur Induced Developmental Delays that Correlate with Behavioral Abnormalities and Altered Expression of hspb9 and hspb11
Shields, J.N., Hales, E.C., Ranspach, L.E., Luo, X., Orr, S., Runft, D., Dombkowski, A., Neely, M.N., Matherly, L.H., Taub, J., Baker, T.R., Thummel, R.
|Source:||Toxics 7(4): (Journal)|
|Registered Authors:||Luo, Xixia, Neely, Melody N., Thummel, Ryan|
|Keywords:||Baygon™, behavior, developmental delays, hspb11, hspb9, insecticide, light-dark test, pesticide, propoxur, zebrafish|
|PubMed:||31546644 Full text @ Toxics|
Shields, J.N., Hales, E.C., Ranspach, L.E., Luo, X., Orr, S., Runft, D., Dombkowski, A., Neely, M.N., Matherly, L.H., Taub, J., Baker, T.R., Thummel, R. (2019) Exposure of Larval Zebrafish to the Insecticide Propoxur Induced Developmental Delays that Correlate with Behavioral Abnormalities and Altered Expression of hspb9 and hspb11. Toxics. 7(4):.
ABSTRACTRecent studies suggest that organophosphates and carbamates affect human fetal development, resulting in neurological and growth impairment. However, these studies are conflicting and the extent of adverse effects due to pesticide exposure warrants further investigation. In the present study, we examined the impact of the carbamate insecticide propoxur on zebrafish development. We found that propoxur exposure delays embryonic development, resulting in three distinct developmental stages: no delay, mild delay, or severe delay. Interestingly, the delayed embryos all physically recovered 5 days after exposure, but behavioral analysis revealed persistent cognitive deficits at later stages. Microarray analysis identified 59 genes significantly changed by propoxur treatment, and Ingenuity Pathway Analysis revealed that these genes are involved in cancer, organismal abnormalities, neurological disease, and hematological system development. We further examined hspb9 and hspb11 due to their potential roles in zebrafish development and found that propoxur increases expression of these small heat shock proteins in all of the exposed animals. However, we discovered that less significant increases were associated with the more severely delayed phenotype. This raises the possibility that a decreased ability to upregulate these small heat shock proteins in response to propoxur exposure may cause embryos to be more severely delayed.
- Genes / Markers (2)