Literature DB >> 19228963

Development of spontaneous recurrent seizures after kainate-induced status epilepticus.

Philip A Williams1, Andrew M White, Suzanne Clark, Damien J Ferraro, Waldemar Swiercz, Kevin J Staley, F Edward Dudek.   

Abstract

Acquired epilepsy (i.e., after an insult to the brain) is often considered to be a progressive disorder, and the nature of this hypothetical progression remains controversial. Antiepileptic drug treatment necessarily confounds analyses of progressive changes in human patients with acquired epilepsy. Here, we describe experiments testing the hypothesis that development of acquired epilepsy begins as a continuous process of increased seizure frequency (i.e., proportional to probability of a spontaneous seizure) that ultimately plateaus. Using nearly continuous surface cortical and bilateral hippocampal recordings with radiotelemetry and semiautomated seizure detection, the frequency of electrographically recorded seizures (both convulsive and nonconvulsive) was analyzed quantitatively for approximately 100 d after kainate-induced status epilepticus in adult rats. The frequency of spontaneous recurrent seizures was not a step function of time (as implied by the "latent period"); rather, seizure frequency increased as a sigmoid function of time. The distribution of interseizure intervals was nonrandom, suggesting that seizure clusters (i.e., short interseizure intervals) obscured the early stages of progression, and may have contributed to the increase in seizure frequency. These data suggest that (1) the latent period is the first of many long interseizure intervals and a poor measure of the time frame of epileptogenesis, (2) epileptogenesis is a continuous process that extends much beyond the first spontaneous recurrent seizure, (3) uneven seizure clustering contributes to the variability in occurrence of epileptic seizures, and (4) the window for antiepileptogenic therapies aimed at suppressing acquired epilepsy probably extends well past the first clinical seizure.

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Year:  2009        PMID: 19228963      PMCID: PMC2897752          DOI: 10.1523/JNEUROSCI.0980-08.2009

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  33 in total

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2.  Excitatory synaptic input to granule cells increases with time after kainate treatment.

Authors:  J P Wuarin; F E Dudek
Journal:  J Neurophysiol       Date:  2001-03       Impact factor: 2.714

3.  The association between seizure clustering and convulsive status epilepticus in patients with intractable complex partial seizures.

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4.  Progression of spontaneous seizures after status epilepticus is associated with mossy fibre sprouting and extensive bilateral loss of hilar parvalbumin and somatostatin-immunoreactive neurons.

Authors:  J A Gorter; E A van Vliet; E Aronica; F H Lopes da Silva
Journal:  Eur J Neurosci       Date:  2001-02       Impact factor: 3.386

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7.  High-frequency oscillations after status epilepticus: epileptogenesis and seizure genesis.

Authors:  Anatol Bragin; Charles L Wilson; Joyel Almajano; Istvan Mody; Jerome Engel
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Review 8.  The course of cellular alterations associated with the development of spontaneous seizures after status epilepticus.

Authors:  F Edward Dudek; Jennifer L Hellier; Philip A Williams; Damien J Ferraro; Kevin J Staley
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  154 in total

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2.  Axon sprouting and synaptic reorganization of GABAergic interneurons: a focused look at a general question.

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5.  Interictal spikes precede ictal discharges in an organotypic hippocampal slice culture model of epileptogenesis.

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Review 8.  Animal models of temporal lobe epilepsy following systemic chemoconvulsant administration.

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9.  The expression of kainate receptor subunits in hippocampal astrocytes after experimentally induced status epilepticus.

Authors:  Jay R Vargas; D Koji Takahashi; Kyle E Thomson; Karen S Wilcox
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10.  Continuous electroencephalographic monitoring with radio-telemetry in a rat model of perinatal hypoxia-ischemia reveals progressive post-stroke epilepsy.

Authors:  Shilpa D Kadam; Andrew M White; Kevin J Staley; F Edward Dudek
Journal:  J Neurosci       Date:  2010-01-06       Impact factor: 6.167

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