Journal
EPILEPSIA
Volume 64, Issue 6, Pages E118-E126Publisher
WILEY
DOI: 10.1111/epi.17580
Keywords
cortico-cortical evoked potential; effective connectivity; intracranial recording; medial temporal lobe epilepsy; responsiveness
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Focal epileptic seizures cause abnormal neuronal discharges, which can spread to other cortical areas and interfere with brain activity, resulting in changes in the patient's experience and behavior. Recent studies have found that medial temporal lobe and neocortical seizures have different effects on synaptic transmission. This study investigates the responsiveness of these areas during seizures, providing insights into the differential impact of seizures on brain networks.
Focal epileptic seizures are characterized by abnormal neuronal discharges that can spread to other cortical areas and interfere with brain activity, thereby altering the patient's experience and behavior. The origin of these pathological neuronal discharges encompasses various mechanisms that converge toward similar clinical manifestations. Recent studies have suggested that medial temporal lobe (MTL) and neocortical (NC) seizures are often underpinned by two characteristic onset patterns, which, respectively, affect and spare synaptic transmission in cortical slices. However, these synaptic alterations and their effects have never been confirmed or studied in intact human brains. To fill this gap, we here evaluate whether responsiveness of MTL and NC are differentially affected by focal seizures, using a unique data set of cortico-cortical evoked potentials (CCEPs) collected during seizures triggered by single-pulse electrical stimulation (SPES). We find that responsiveness is abruptly reduced by the onset of MTL seizures, despite increased spontaneous activity, whereas it is preserved in the case of NC seizures. The present results provide an extreme example of dissociation between responsiveness and activity and show that brain networks are diversely affected by the onset of MTL and NC seizures, thus extending at the whole brain level the evidence of synaptic alteration found in vitro.
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