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Published on: April 14, 2021
Zebrafish as an Alternative Animal Model of Huntington's Disease: Challenges and Future Directions
Jiahao Cui1,2, Zhili Yu1,2, Zhike Fu1,2
1Suzhou Key Laboratory of Neurobiology and Cell Signaling, School of Science, Xi'an Jiaotong-Liverpool University, 215123 Suzhou, Jiangsu, China.
Abstract:
Huntington's disease (HD) is a lethal autosomal dominant neurodegenerative disorder characterized by progressing cognitive, motor, and other behavioral deficits. Animal models, especially rodent-based, are a valuable tool to study brain disorders, including HD. Given the existence of multiple valid and predictive models of HD and other brain disorders, we are now entering a phase of mechanistic discovery, as research shifts towards phenotype-based screening and multi-omic validation. In addition to rodent models, zebrafish (Danio rerio) are rapidly becoming a promising model organism for translational HD research. With considerable genetic homology to humans, embryonic transparency for real-time pathology tracking, physiological similarity to mammals, and high-throughput drug screening potential, zebrafish have become a valuable alternative model organism in translational HD research. Here, we discuss zebrafish HD models, their advantages and limitations, and future directions of translational research in this field.

