PUBLICATION

Optimization of a locomotion-based zebrafish seizure model

Authors
Shaw, P.A.G., Panda, S.K., Stanca, A., Luyten, W.
ID
ZDB-PUB-220415-9
Date
2022
Source
Journal of Neuroscience Methods   375: 109594 (Journal)
Registered Authors
Keywords
Locomotor assay, Pentylenetetrazol, Seizure model, Valproate, Zebrafish
MeSH Terms
  • Animals
  • Anticonvulsants*/pharmacology
  • Anticonvulsants*/therapeutic use
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Larva
  • Locomotion
  • Pentylenetetrazole/toxicity
  • Seizures/chemically induced
  • Seizures/prevention & control
  • Zebrafish*
PubMed
35421798 Full text @ J. Neurosci. Methods
Abstract
Locomotor assays in zebrafish have emerged as a screening test in early drug discovery for antiseizure compounds. However, parameters differ considerably between published studies, which may explain some discrepant results with (candidate) antiseizure medications.
We optimized a locomotor-based seizure assay in zebrafish with pentylenetetrazol (PTZ) as the pharmacological proconvulsant to generate a therapeutic window in which proconvulsant-treated zebrafish larvae could be discriminated from a non-treated control. To generate a reliable control, exposure time and concentration of valproate (VPA, anticonvulsant) was optimized.
Wells with one or three larvae show a similar PTZ dose-dependent increase in locomotion with less variability in motility for the latter. Zebrafish immersed in 10 mM PTZ showed a significant increase in movement with a sustained effect, without any indication of toxicity. Animals treated with 3 mM VPA showed the strongest reduction of PTZ-induced movement without toxicity. The decrease in PTZ-induced locomotion was greater after 18 h versus 2 h.
For the larval zebrafish PTZ-induced seizure model, varying experimental parameters have been reported in literature. Our results show that PTZ is often used at toxic concentrations, and we provide instead reliable conditions to quantify convulsant behaviour using an infrared-beam motility assay.
We recommend using three zebrafish larvae per well to quantify locomotion in 96-multiwell plates. Larvae should preferably be exposed to 10 mM PTZ for 1 h, consisting of 30 min acclimation and 30 min subsequent recording. As positive control for anticonvulsant activity, we recommend exposure to 3 mM VPA for 18 h before administration of PTZ.
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