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Cerebral Cortex Advance Access published online on October 13, 2004

Cerebral Cortex, doi:10.1093/cercor/bhh184
© 2004 by Oxford University Press
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Article

Homeostatic Synaptic Plasticity Can Explain Post-traumatic Epileptogenesis in Chronically Isolated Neocortex

Arthur R. Houweling 1*, Maxim Bazhenov 2, Igor Timofeev 3, Mircea Steriade 3, and Terrence J. Sejnowski 4

1 The Salk Institute, Computational Neurobiology Laboratory, La Jolla, CA 92037, USA; Program in Neurosciences, University of California San Diego, La Jolla, CA 92093, USA
2 The Salk Institute, Computational Neurobiology Laboratory, La Jolla, CA 92037, USA
3 Laboratoire de Neurophysiologie, Université Laval, Québec, Canada G1K 7P4
4 The Salk Institute, Computational Neurobiology Laboratory, La Jolla, CA 92037, USA; Division of Biological Sciences, University of California San Diego, La Jolla, CA 92093, USA

* To whom correspondence should be addressed. E-mail: arthur{at}salk.edu.


   Abstract

Chronically isolated neocortex develops chronic hyperexcitability and focal epileptogenesis in a period of days to weeks. The mechanisms operating in this model of post-traumatic epileptogenesis are not well understood. We hypothesized that the spontaneous burst discharges recorded in chronically isolated neocortex result from homeostatic plasticity (a mechanism generally assumed to stabilize neuronal activity) induced by low neuronal activity after deafferentation. To test this hypothesis we constructed computer models of neocortex incorporating a biologically based homeostatic plasticity rule that operates to maintain firing rates. After deafferentation, homeostatic upregulation of excitatory synapses on pyramidal cells, either with or without concurrent downregulation of inhibitory synapses or upregulation of intrinsic excitability, initiated slowly repeating burst discharges that closely resembled the epileptiform burst discharges recorded in chronically isolated neocortex. These burst discharges lasted a few hundred ms, propagated at 1-3 cm/s and consisted of large (10-15 mV) intracellular depolarizations topped by a small number of action potentials. Our results support a role for homeostatic synaptic plasticity as a novel mechanism of post-traumatic epileptogenesis.

Keywords: brain trauma; computational model; deafferentation; epilepsy; injury; slow oscillation.
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