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The Journal of Neurophysiology Vol. 83 No. 3 March 2000, pp. 1115-1124
Copyright ©2000 by the American Physiological Society
1Departments of Neurology and Neurosurgery, and Physiology, Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada; and 2Centre Paul Broca and Institut National de la Santé et de la Recherche Médicale U109, 75014 Paris, France
Barbarosie, Michaela,
Jacques Louvel,
Irène Kurcewicz, and
Massimo Avoli.
CA3-Released Entorhinal Seizures Disclose Dentate Gyrus
Epileptogenicity and Unmask a Temporoammonic Pathway. J. Neurophysiol. 83: 1115-1124, 2000. We have
investigated the propagation of epileptiform discharges induced by
4-aminopyridine (4-AP, 50 µM) in adult mouse hippocampus-entorhinal cortex slices, before and after Schaffer collateral cut. 4-AP application induced 1) ictal epileptiform activity that
disappeared over time and 2) interictal epileptiform
discharges, which continued throughout the experiment. Using
simultaneous field potential and [K+]o
recordings, we found that entorhinal and dentate ictal epileptiform discharges were accompanied by comparable elevations in
[K+]o (up to 12 mM from a baseline value of
3.2 mM), whereas smaller rises in [K+]o (up
to 6 mM) were associated with ictal activity in CA3. Cutting the
Schaffer collaterals disclosed the occurrence of ictal discharges that
were associated with larger rises in [K+]o as
compared with the intact slice. Further lesion of the perforant path
blocked ictal activity and the associated
[K+]o increases in the dentate gyrus,
indicating synaptic propagation to this area. Time delay measurements
demonstrated that ictal epileptiform activity in the intact
hippocampal-entorhinal cortex slice propagated via the trisynaptic
path. However, after Schaffer collateral cut, ictal discharges
continued to occur in CA1 and subiculum and spread to these areas
directly from the entorhinal cortex. Thus our data indicate that the
increased epileptogenicity of the dentate gyrus (a prominent feature of
temporal lobe epilepsy as well), may depend on perforant path
propagation of entorhinal ictal discharges, irrespective of mossy fiber
reorganization. Moreover, hippocampal neuronal damage that is acutely
mimicked in our model by Schaffer collateral cut, may contribute to
"short-circuit" propagation of activity by pathways that are masked
when the hippocampus is intact.
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