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Kinase Inhibitors with Antiepileptic Properties Identified with a Novel in Vitro Screening Platform

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Kinase signaling plays an important role in acquired epilepsy, but only a small percentage of the total kinome has been investigated in this context. A major roadblock that prevents the systematic investigation of the contributions of kinase signaling networks is the slow speed of experiments designed to test the chronic effects of target inhibition in epilepsy models. We developed a novel in vitro screening platform based on microwire recordings from an organotypic hippocampal culture model of acquired epilepsy. This platform enables the direct, parallel determination of the effects of compounds on spontaneous epileptiform activity. The platform also enables repeated recordings from the same culture over two-week long experiments. We screened 45 kinase inhibitors and quantified their effects on seizure duration, the frequency of paroxysmal activity, and electrographic load. We identified several inhibitors with previously unknown antiepileptic properties. We also used kinase inhibition profile cross-referencing to identify kinases that are inhibited by seizure-suppressing compounds, but not by compounds that had no effect on seizures.

Contributor(s)
Publisher
MDPI AG
Date Issued
2019-05-21
Language
English
Type
Genre
Form
electronic document
Media type
Creator role
Faculty
Identifier
1422-0067
Has this item been published elsewhere?
Volume
20
Volume
10
Liu, . J., Schenker, . M., Ghiasvand, . S., & Berdichevsky, . Y. (2019). (Vols. 10). https://doi.org/10.3390/ijms20102502
Liu, Jing, Madison Schenker, Shabnam Ghiasvand, and Yevgeny Berdichevsky. 2019. https://doi.org/10.3390/ijms20102502.
Liu, Jing, et al. 21 May 2019, https://doi.org/10.3390/ijms20102502.