Development of a rat model for glioma-related epilepsy

Seizures are common in patients with high-grade gliomas (30–60%) and approximately 15–30% of glioblastoma (GB) patients develop drug-resistant epilepsy. Reliable animal models are needed to develop adequate treatments for glioma-related epilepsy. Therefore, fifteen rats were inoculated with F98 GB c...

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Hauptverfasser: Bouckaert, Charlotte, Germonpré, Charlotte, Verhoeven, Jeroen, Chong, Seon-Ah, Jacquin, Lucas, Mairet-Coello, Georges, André, Véronique Marie, Leclercq, Karine, Vanhove, Christian, De Vos, Filip, Van den Broecke, Caroline, Goethals, Ingeborg, Descamps, Benedicte, Donche, Sam, Carrette, Evelien, Wadman, Wytse, Boon, Paul, Vonck, Kristl, Raedt, Robrecht
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creator Bouckaert, Charlotte
Germonpré, Charlotte
Verhoeven, Jeroen
Chong, Seon-Ah
Jacquin, Lucas
Mairet-Coello, Georges
André, Véronique Marie
Leclercq, Karine
Vanhove, Christian
De Vos, Filip
Van den Broecke, Caroline
Goethals, Ingeborg
Descamps, Benedicte
Donche, Sam
Carrette, Evelien
Wadman, Wytse
Boon, Paul
Vonck, Kristl
Raedt, Robrecht
description Seizures are common in patients with high-grade gliomas (30–60%) and approximately 15–30% of glioblastoma (GB) patients develop drug-resistant epilepsy. Reliable animal models are needed to develop adequate treatments for glioma-related epilepsy. Therefore, fifteen rats were inoculated with F98 GB cells (GB group) and four rats with vehicle only (control group) in the right entorhinal cortex. MRI was performed to visualize tumor presence. A subset of seven GB and two control rats were implanted with recording electrodes to determine the occurrence of epileptic seizures with video-EEG recording over multiple days. In a subset of rats, tumor size and expression of tumor markers were investigated with histology or mRNA in situ hybridization. Tumors were visible on MRI six days post-inoculation. Time-dependent changes in tumor morphology and size were visible on MRI. Epileptic seizures were detected in all GB rats monitored with video-EEG. Twenty-one days after inoculation, rats were euthanized based on signs of discomfort and pain. This study describes, for the first time, reproducible tumor growth and spontaneous seizures upon inoculation of F98 cells in the rat entorhinal cortex. The development of this new model of GB-related epilepsy may be valuable to design new therapies against tumor growth and associated epileptic seizures.
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Reliable animal models are needed to develop adequate treatments for glioma-related epilepsy. Therefore, fifteen rats were inoculated with F98 GB cells (GB group) and four rats with vehicle only (control group) in the right entorhinal cortex. MRI was performed to visualize tumor presence. A subset of seven GB and two control rats were implanted with recording electrodes to determine the occurrence of epileptic seizures with video-EEG recording over multiple days. In a subset of rats, tumor size and expression of tumor markers were investigated with histology or mRNA in situ hybridization. Tumors were visible on MRI six days post-inoculation. Time-dependent changes in tumor morphology and size were visible on MRI. Epileptic seizures were detected in all GB rats monitored with video-EEG. Twenty-one days after inoculation, rats were euthanized based on signs of discomfort and pain. This study describes, for the first time, reproducible tumor growth and spontaneous seizures upon inoculation of F98 cells in the rat entorhinal cortex. 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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; MDPI - Multidisciplinary Digital Publishing Institute; Ghent University Academic Bibliography; PubMed Central
subjects BRAIN-TUMOR
Catalysis
Computer Science Applications
General Medicine
glioma
glioma-related epilepsy
GLUTAMATE
high-grade glioma rat model
Inorganic Chemistry
MANAGEMENT
Medicine and Health Sciences
Molecular Biology
Organic Chemistry
PATHOPHYSIOLOGY
Physical and Theoretical Chemistry
seizures
Spectroscopy
TUMOR-ASSOCIATED EPILEPSY
video-EEG monitoring
title Development of a rat model for glioma-related epilepsy
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