This paper focuses on high-frequency (gamma band) EEG activity, the most characteristic electrophysiological pattern in focal seizures of human epilepsy. It starts with recent hypotheses about: (i) the behaviour of inhibitory interneurons in hippocampal or neocortical networks in the generation of gamma frequency oscillations; (ii) the nonuniform alteration of GABAergic inhibition in experimental epilepsy (reduced dendritic inhibition and increased somatic inhibition); and (iii) the possible depression of GABA(A,fast) circuit activity by GABA(A,slow) inhibitory postsynaptic currents. In particular, these hypotheses are introduced in a new computational macroscopic model of EEG activity that includes a physiologically relevant fast inhibitory feedback loop. Results show that strikingly realistic activity is produced by the model when compared to real EEG signals recorded with intracerebral electrodes. They show that, in the model, the transition from interictal to fast ictal activity is explained by the impairment of dendritic inhibition.

The identification of brain regions generating seizures ('epileptogenic zone', EZ) in patients with refractory partial epilepsy is crucial prior to surgery. During pre-surgical evaluation, this identification can be performed from the analysis of intracerebral EEG. In particular, the presence of high-frequency oscillations, often referred to as 'rapid discharges', has long been recognized as a characteristic electrophysiological pattern of the EZ. However, to date, there has been no attempt to make use of this specific pattern to quantitatively evaluate the degree of epileptogenicity in recorded structures. A novel quantitative measure that characterizes the epileptogenicity of brain structures recorded with depth electrodes is presented. This measure, called 'Epileptogenicity Index' (EI), is based on both spectral (appearance of fast oscillations replacing the background activity) and temporal (delay of appearance with respect to seizure onset) properties of intracerebral EEG signals. EI values were computed in mesial and lateral structures of the temporal lobe in a group of 17 patients with mesial temporal lobe epilepsy (MTLE). Statistically high EI values corresponded to structures involved early in the ictal process and producing rapid discharges at seizure onset. In all patients, these high values were obtained in more than one structure of the temporal lobe region. In the majority of patients, highest EI values were computed from signals recorded in mesial structures. In addition, when averaged over patients, EI values gradually decreased from structure to structure. For lateral neocortex, higher EI values were found in patients with normal MRI, in contrast with patients with hippocampal sclerosis. In this former sub-group of patients, a greater number of epileptogenic structures was also found. A statistically significant correlation was found between the duration of epilepsy and the number of structures disclosing high epileptogenicity suggesting that MTLE is a gradually evolving process in which the epileptogenicity of the temporal lobe tends to increase with time.