Increased Dentate Gyrus Excitability in the Intrahippocampal Kainic Acid Mouse Model for Temporal Lobe Epilepsy.

dentate gyrus (DG) field postsynaptic potential (fPSP) intrahippocampal kainic acid (IHKA) mouse model multielectrode array (MEA) temporal lobe epilepsy (TLE)

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
04 Jan 2024
Historique:
received: 29 11 2023
revised: 29 12 2023
accepted: 02 01 2024
medline: 11 1 2024
pubmed: 11 1 2024
entrez: 11 1 2024
Statut: epublish

Résumé

The intrahippocampal kainic acid (IHKA) mouse model is an extensively used in vivo model to investigate the pathophysiology of mesial temporal lobe epilepsy (mTLE) and to develop novel therapies for drug-resistant epilepsy. It is characterized by profound hippocampal sclerosis and spontaneously occurring seizures with a major role for the injected damaged hippocampus, but little is known about the excitability of specific subregions. The purpose of this study was to electrophysiologically characterize the excitability of hippocampal subregions in the chronic phase of the induced epilepsy in the IHKA mouse model. We recorded field postsynaptic potentials (fPSPs) after electrical stimulation in the CA1 region and in the dentate gyrus (DG) of hippocampal slices of IHKA and healthy mice using a multielectrode array (MEA). In the DG, a significantly steeper fPSP slope was found, reflecting higher synaptic strength. Population spikes were more prevalent with a larger spatial distribution in the IHKA group, reflecting a higher degree of granule cell output. Only minor differences were found in the CA1 region. These results point to increased neuronal excitability in the DG but not in the CA1 region of the hippocampus of IHKA mice. This method, in which the excitability of hippocampal slices from IHKA mice is investigated using a MEA, can now be further explored as a potential new model to screen for new interventions that can restore DG function and potentially lead to novel therapies for mTLE.

Identifiants

pubmed: 38203829
pii: ijms25010660
doi: 10.3390/ijms25010660
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Research Foundation - Flanders
ID : G042219N
Organisme : Ghent University Special Research Fund
ID : BOF22/GOA/027

Auteurs

Marijke Vergaelen (M)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Simona Manzella (S)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Kristl Vonck (K)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Erine Craey (E)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Jeroen Spanoghe (J)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Mathieu Sprengers (M)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Evelien Carrette (E)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Wytse Jan Wadman (WJ)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Jean Delbeke (J)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Paul Boon (P)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Lars Emil Larsen (LE)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.
MEDISIP, Department of Electronics and Information Systems, Ghent University, 9000 Ghent, Belgium.

Robrecht Raedt (R)

4BRAIN, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.

Classifications MeSH