The intrinsic cellular, synaptic and network mechanisms underlying cortically-initiated electrographical seizures will be explored with electrophysiological experiments in vivo and in computational modeling I studies. The electrographical seizures observed in cat neocortex resemble partial and generalized epileptic | seizures consisting of spike-wave (SW) or polyspike-wave (PSW) complexes at 1.5 about Hz and fast runs at 10 15 Hz. We will study (a) specific cellular and network mechanisms responsible for the onset, maintenance and I termination of the paroxysmal seizures; (b) the specific and common properties of different types of | electrographical seizures; (c) the conditions responsible for transforming spatially localized paroxysmal activity into generalized seizure. Compartmental models of excitatory and inhibitory neocortical neurons and their interactions will be used to examine specific hypotheses for the mechanisms underlying multiple intracortical processes preceding, accompanying and following electrographic seizures and to generate predictions that can be tested experimentally. These models may also be useful for preliminary screening of antiepileptic drags. The methods that will be used in these studies include (a) in vivo multisided intracellular and l field potential recordings from anesthetized and behaving animals to probe specific intracellular and synaptic changes during seizure; (b) recently developed independent component analysis (ICA) applied to the I electrophysiological data to study spatio-temporal properties of paroxysmal activity; (c) computational modeling based on detailed description of the intrinsic properties of individual neurons and their synaptic interconnections. The modeling techniques are aimed at understanding paroxysmal seizure mechanisms by simultaneous and independent observations of all contributing factors, some of which are difficult to study experimentally. Electrophysiological recordings and preliminary analysis of the experimental data will beconducted in Laval University (Canada) and detailed computational analysis based on ICA methods and modeling techniques will be conducted in the Salk Institute (USA). These studies may lead to new treatments for epilepsy based on comparisons between models for the normal and diseased states of the cortex.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS040522-03
Application #
6529022
Study Section
Special Emphasis Panel (ZRG1-BDCN-2 (01))
Program Officer
Chen, Daofen
Project Start
2000-09-30
Project End
2004-08-31
Budget Start
2002-09-01
Budget End
2004-08-31
Support Year
3
Fiscal Year
2002
Total Cost
$264,700
Indirect Cost
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
005436803
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Lainscsek, Claudia; Sejnowski, Terrence J (2015) Delay differential analysis of time series. Neural Comput 27:594-614
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Lainscsek, Claudia; Sejnowski, Terrence J (2013) Electrocardiogram classification using delay differential equations. Chaos 23:023132
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Nita, Dragos A; Cisse, Youssouf; Timofeev, Igor et al. (2006) Increased propensity to seizures after chronic cortical deafferentation in vivo. J Neurophysiol 95:902-13
Steriade, Mircea (2006) Neuronal substrates of spike-wave seizures and hypsarrhythmia in corticothalamic systems. Adv Neurol 97:149-54
Steriade, Mircea (2005) Sleep, epilepsy and thalamic reticular inhibitory neurons. Trends Neurosci 28:317-24
Houweling, Arthur R; Bazhenov, Maxim; Timofeev, Igor et al. (2005) Homeostatic synaptic plasticity can explain post-traumatic epileptogenesis in chronically isolated neocortex. Cereb Cortex 15:834-45

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