Identification of compounds with anti-convulsant properties in a zebrafish model of epileptic seizures

被引:118
作者
Baxendale, Sarah [1 ]
Holdsworth, Celia J. [1 ]
Santoscoy, Paola L. Meza [1 ]
Harrison, Michael R. M. [1 ]
Fox, James [1 ]
Parkin, Caroline A. [1 ]
Ingham, Philip W. [1 ]
Cunliffe, Vincent T. [1 ]
机构
[1] Univ Sheffield, Dept Biomed Sci, MRC Ctr Dev & Biomed Genet, Sheffield S10 2TN, S Yorkshire, England
关键词
ANTIEPILEPTIC DRUGS; GABA(A) RECEPTORS; SYNAPSE DEVELOPMENT; IMPORTANT ISSUES; ADULT ZEBRAFISH; NEURAL ACTIVITY; NEUROPEPTIDE-Y; MICE; MECHANISMS; BEHAVIOR;
D O I
10.1242/dmm.010090
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The availability of animal models of epileptic seizures provides opportunities to identify novel anticonvulsants for the treatment of people with epilepsy. We found that exposure of 2-day-old zebrafish embryos to the convulsant agent pentylenetetrazole (PTZ) rapidly induces the expression of synaptic-activity-regulated genes in the CNS, and elicited vigorous episodes of calcium (Ca2+) flux in muscle cells as well as intense locomotor activity. We then screened a library of similar to 2000 known bioactive small molecules and identified 46 compounds that suppressed PTZ-induced transcription of the synaptic-activity-regulated gene fos in 2-day-old (2 dpf) zebrafish embryos. Further analysis of a subset of these compounds, which included compounds with known and newly identified anticonvulsant properties, revealed that they exhibited concentration-dependent inhibition of both locomotor activity and PTZ-induced fos transcription, confirming their anticonvulsant characteristics. We conclude that this in situ hybridisation assay for fos transcription in the zebrafish embryonic CNS is a robust, high-throughput in vivo indicator of the neural response to convulsant treatment and lends itself well to chemical screening applications. Moreover, our results demonstrate that suppression of PTZ-induced fos expression provides a sensitive means of identifying compounds with anticonvulsant activities.
引用
收藏
页码:773 / 784
页数:12
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