Literature DB >> 10717428

Changes in neuronal conductance during different components of cortically generated spike-wave seizures.

D Neckelmann1, F Amzica, M Steriade.   

Abstract

Neuronal conductance was studied in anesthetized cats during cortically generated spike-wave seizures arising from slow sleep oscillation. Single and dual intracellular recordings from neocortical neurons were used. The changes were similar whether the seizures occurred spontaneously, or were evoked by electrical stimulation or induced by bicuculline. In all seizures, the conductance increased from the very onset of the seizure and returned to control values only at the end of the postictal depression. Simultaneous intracellular recordings from two neurons showed that the neuron leading the other neuron displayed the largest increase in membrane conductance. The changes in neuronal conductance during the two phases of the slow sleep oscillation, i.e. highest during depolarizations and lowest during hyperpolarizations, were similar to those occurring during the "spike" and "wave" components of seizures. (1) Maximal conductance was found during the paroxysmal depolarizing shift corresponding to the electroencephalogram "spike" (median: 252 nS; range: 90 to more than 400 nS). It was highest at the onset of the depolarized plateau and decreased thereafter. (2) During the hyperpolarization corresponding to the electroencephalogram "wave", the conductance was significantly lower (median: 71 nS; range: 41 to 140 nS). (3) The conductance was elevated during the fast runs (median: 230 nS; range: 92 to 350 nS) which occurred in two-thirds of the seizures. (4) The conductance values during postictal depression were situated between those measured during the seizure hyperpolarizations and during sleep hyperpolarizations. The conductance decreased exponentially back to the values of the slow sleep oscillation over the total duration of the postictal depression. The data suggest that the major mechanism underlying the "wave"-related hyperpolarizing component of spike-wave seizures relies mainly not on active inhibition, but on a mixture of disfacilitation and potassium currents.

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Year:  2000        PMID: 10717428     DOI: 10.1016/s0306-4522(99)00571-0

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  19 in total

1.  Origin of synchronized oscillations induced by neocortical disinhibition in vivo.

Authors:  M A Castro-Alamancos
Journal:  J Neurosci       Date:  2000-12-15       Impact factor: 6.167

2.  Cortical hyperpolarization-activated depolarizing current takes part in the generation of focal paroxysmal activities.

Authors:  Igor Timofeev; Maxim Bazhenov; Terrence Sejnowski; Mircea Steriade
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-27       Impact factor: 11.205

3.  High-frequency changes during interictal spikes detected by time-frequency analysis.

Authors:  Julia Jacobs; Katsuhiro Kobayashi; Jean Gotman
Journal:  Clin Neurophysiol       Date:  2010-07-06       Impact factor: 3.708

4.  Seizure-like afterdischarges simulated in a model neuron.

Authors:  H Kager; W J Wadman; G G Somjen
Journal:  J Comput Neurosci       Date:  2007-04       Impact factor: 1.621

5.  Focal generation of paroxysmal fast runs during electrographic seizures.

Authors:  Sofiane Boucetta; Sylvain Chauvette; Maxim Bazhenov; Igor Timofeev
Journal:  Epilepsia       Date:  2008-06-26       Impact factor: 5.864

6.  Intracellular activity of cortical and thalamic neurones during high-voltage rhythmic spike discharge in Long-Evans rats in vivo.

Authors:  Pierre-Olivier Polack; Stéphane Charpier
Journal:  J Physiol       Date:  2006-01-12       Impact factor: 5.182

7.  Negative BOLD response to interictal epileptic discharges in focal epilepsy.

Authors:  Francesca Pittau; Firas Fahoum; Rina Zelmann; François Dubeau; Jean Gotman
Journal:  Brain Topogr       Date:  2013-06-22       Impact factor: 3.020

8.  Detection of changes of high-frequency activity by statistical time-frequency analysis in epileptic spikes.

Authors:  Katsuhiro Kobayashi; Julia Jacobs; Jean Gotman
Journal:  Clin Neurophysiol       Date:  2009-04-25       Impact factor: 3.708

9.  Deep layer somatosensory cortical neurons initiate spike-and-wave discharges in a genetic model of absence seizures.

Authors:  Pierre-Olivier Polack; Isabelle Guillemain; Emilie Hu; Colin Deransart; Antoine Depaulis; Stéphane Charpier
Journal:  J Neurosci       Date:  2007-06-13       Impact factor: 6.167

10.  A model for focal seizure onset, propagation, evolution, and progression.

Authors:  Jyun-You Liou; Elliot H Smith; Lisa M Bateman; Samuel L Bruce; Guy M McKhann; Robert R Goodman; Ronald G Emerson; Catherine A Schevon; L F Abbott
Journal:  Elife       Date:  2020-03-23       Impact factor: 8.140

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