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J Neurophysiol (December 1, 2002). 10.1152/jn.00211.2002
Submitted on 21 March 2002
Accepted on 27 August 2002
Neuronal Networks Group, Department of Physiology and Biophysics, St. Mary's Hospital Medical School, Imperial College of Science, Technology and Medicine, London W2 1PG, United Kingdom
Finnerty, G. T. and
J.G.R. Jefferys.
Investigation of the Neuronal Aggregate Generating Seizures in
the Rat Tetanus Toxin Model of Epilepsy. J. Neurophysiol. 88: 2919-2927, 2002. A key question in epilepsy is
the organization and size of the neuronal networks necessary for
generating seizures. Hypotheses include: a single focal neuronal
network drives seizure discharges across the brain, which may or may
not be identical with the circuits that generate interictal spikes; or
multiple neuronal networks link together in re-entrant loops or other
long-range networks. It remains unclear whether any of these hypotheses
apply to spontaneous seizures in freely moving animals. We used the
tetanus toxin chronic model of epilepsy to test the different
predictions made by each hypothesis about the propagation and
interaction of epileptic discharges during seizures. Seizures could
start in either the injected or noninjected dorsal hippocampus,
suggesting that seizures have multifocal onsets in the tetanus toxin
model. During seizures, individual bursts propagated in either
direction, both between the right and left dorsal hippocampi, and
between CA3 and the dentate gyrus in the same hippocampus. These
findings argue against one site "driving" seizures or seizures
propagating around a limbic loop. Specifically, the side leading each
burst switched a median of three times during the first 20 s of a
seizure. Analysis of bursts during seizures suggested that the network
at each recording site acted like a neuronal oscillator. Coupling of
population spikes in right and left CA3 increased during the early part
of seizures, but the cross-correlation of their whole-discharge
waveforms changed little over the same period. Furthermore, the
polarity of the phase difference between population spikes did not
follow the phase difference for complete discharges. We concluded that the neuronal aggregate necessary for seizures in our animals comprises multiple spatially distributed neuronal networks and that the increased
synchrony of the output (population spike firing) of these networks
during the early part of seizures may contribute to seizure generation.
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