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Analysis of Intracerebral EEG Recordings of Epileptic Spikes: Insights From a Neural Network Model

The pathophysiological interpretation of EEG signals recorded with depth electrodes [i.e., local field potentials (LFPs)] during interictal (between seizures) or ictal (during seizures) periods is fundamental in the presurgical evaluation of patients with drug-resistant epilepsy. Our objective was t...

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Bibliographic Details
Published in:IEEE transactions on biomedical engineering 2009-12, Vol.56 (12), p.2782-2795
Main Authors: Demont-Guignard, Sophie, Benquet, Pascal, Gerber, Urs, Wendling, Fabrice
Format: Article
Language:English
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Summary:The pathophysiological interpretation of EEG signals recorded with depth electrodes [i.e., local field potentials (LFPs)] during interictal (between seizures) or ictal (during seizures) periods is fundamental in the presurgical evaluation of patients with drug-resistant epilepsy. Our objective was to explain specific shape features of interictal spikes in the hippocampus (observed in LFPs) in terms of cell- and network-related parameters of neuronal circuits that generate these events. We developed a neural network model based on ldquominimalrdquo but biologically relevant neuron models interconnected through GABAergic and glutamatergic synapses that reproduce the main physiological features of the CA1 subfield. Simulated LFPs were obtained by solving the forward problem (dipole theory) from networks including a large number (~3000) of cells. Insertion of appropriate parameters allowed the model to simulate events that closely resemble actual epileptic spikes. Moreover, the shape of the early fast component (ldquospikerdquo) and the late slow component (ldquonegative waverdquo) was linked to the relative contribution of glutamatergic and GABAergic synaptic currents in pyramidal cells. In addition, the model provides insights about the sensitivity of electrode localization with respect to recorded tissue volume and about the relationship between the LFP and the intracellular activity of principal cells and interneurons represented in the network.
ISSN:0018-9294
1558-2531
DOI:10.1109/TBME.2009.2028015