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Low-voltage fast seizures in humans begin with increased interneuron firing
Journal article   Open access   Peer reviewed

Low-voltage fast seizures in humans begin with increased interneuron firing

Bahareh Elahian, Nathan E Lado, Emily Mankin, Sitaram Vangala, Amrit Misra, Karen Moxon, Itzhak Fried, Ashwini Sharan, Mohammed Yeasin, Richard Staba, …
Annals of neurology, v 84(4), pp 588-600
Oct 2018
PMID: 30179277
url
https://europepmc.org/articles/pmc6814155View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

Action Potentials - physiology Adult Electrodes, Implanted - trends Electroencephalography - methods Electroencephalography - trends Female Gyrus Cinguli - physiopathology Humans Interneurons - physiology Male Middle Aged Retrospective Studies Seizures - diagnosis Seizures - physiopathology Temporal Lobe - physiopathology Young Adult
Intracellular recordings from cells in entorhinal cortex tissue slices show that low-voltage fast (LVF) onset seizures are generated by inhibitory events. Here, we determined whether increased firing of interneurons occurs at the onset of spontaneous mesial-temporal LVF seizures recorded in patients. The seizure onset zone (SOZ) was identified using visual inspection of the intracranial electroencephalogram. We used wavelet clustering and temporal autocorrelations to characterize changes in single-unit activity during the onset of LVF seizures recorded from microelectrodes in mesial-temporal structures. Action potentials generated by principal neurons and interneurons (ie, putative excitatory and inhibitory neurons) were distinguished using waveform morphology and K-means clustering. From a total of 200 implanted microelectrodes in 9 patients during 13 seizures, we isolated 202 single units; 140 (69.3%) of these units were located in the SOZ, and 40 (28.57%) of them were classified as inhibitory. The waveforms of both excitatory and inhibitory units remained stable during the LVF epoch (p > > 0.05). In the mesial-temporal SOZ, inhibitory interneurons increased their firing rate during LVF seizure onset (p < 0.01). Excitatory neuron firing rates peaked 10 seconds after the inhibitory neurons (p < 0.01). During LVF spread to the contralateral mesial temporal lobe, an increase in inhibitory neuron firing rate was also observed (p < 0.01). Our results suggest that seizure generation and spread during spontaneous mesial-temporal LVF onset events in humans may result from increased inhibitory neuron firing that spawns a subsequent increase in excitatory neuron firing and seizure evolution. Ann Neurol 2018;84:588-600.

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Collaboration types
Domestic collaboration
International collaboration
Web of Science research areas
Clinical Neurology
Neurosciences
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