PUBLICATION
Early life stage transient aristolochic acid exposure induces behavioral hyperactivity but not nephrotoxicity in larval zebrafish
- Authors
- Chen, J., Kong, A., Shelton, D., Dong, H., Li, J., Zhao, F., Bai, C., Huang, K., Mo, W., Chen, S., Xu, H., Tanguay, R.L., Dong, Q.
- ID
- ZDB-PUB-210728-24
- Date
- 2021
- Source
- Aquatic toxicology (Amsterdam, Netherlands) 238: 105916 (Journal)
- Registered Authors
- Tanguay, Robyn L.
- Keywords
- Aristolochic acids, Motor neuron, Neurobehavioral toxicity, Oxidative stress, Vision
- MeSH Terms
- none
- PubMed
- 34303159 Full text @ Aquat. Toxicol.
Citation
Chen, J., Kong, A., Shelton, D., Dong, H., Li, J., Zhao, F., Bai, C., Huang, K., Mo, W., Chen, S., Xu, H., Tanguay, R.L., Dong, Q. (2021) Early life stage transient aristolochic acid exposure induces behavioral hyperactivity but not nephrotoxicity in larval zebrafish. Aquatic toxicology (Amsterdam, Netherlands). 238:105916.
Abstract
Aristolochic acids (AA) are nitrophenanthrene carboxylic acids found in plants of the Aristolochiaceae family. Humans are exposed to AA by deliberately taking herbal medicines or unintentionally as a result of environmental contamination. AA is notorious for its nephrotoxicity, however, fewer studies explore potential neurotoxicity associated with AA exposure. The developing nervous system is vulnerable to xenobiotics, and pregnant women exposed to AA may put their fetuses at risk. In the present study, we used the embryonic zebrafish model to evaluate the developmental neurotoxicity associated with AA exposure. At non-teratogenic concentrations (≤ 4 µM), continuous AA exposure from 8 to 120 hours post fertilization (hpf) resulted in larval hyperactivity that was characterized by increased moving distance, elevated activity and faster swimming speeds in several behavioral assays. Further analysis revealed that 8-24 hpf is the most sensitive exposure window for AA-induced hyperactivity. AA exposures specifically increased motor neuron proliferation, increased apoptosis in the eye, and resulted in cellular oxidative stress. In addition, AA exposures increased larval eye size and perturbed the expression of vision genes. Our study, for the first time, demonstrates that AA is neurotoxic to the developmental zebrafish with a sensitive window distinct from its well-documented nephrotoxicity.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping