Literature DB >> 8782868

Interspike intervals during interictal periods in human temporal lobe epilepsy.

B W Colder1, C L Wilson, R C Frysinger, R M Harper, J Engel.   

Abstract

We recorded 259 single neurons from mesial temporal lobe structures of 21 patients with complex partial seizures. Interspike intervals within clusters of action potentials (clustered interspike intervals) recorded from cells in mesial temporal structures ipsilateral to seizure initiation were compared to clustered interspike intervals in the contralateral temporal lobe. 'Clusters' were defined as any group of three or more spikes separated by intervals of less than a defined maximum, or two spikes separated by less than half that maximum. The maximum interspike interval which defined a cluster was varied from 5 to 40 ms in 5-ms steps. Significantly smaller proportions of clustered spikes were discharged by neurons in the amygdala, hippocampus and entorhinal cortex from the temporal lobe commonly initiating seizures, compared to neurons in contralateral homotopic regions. When data from the same three structures were combined, significantly fewer cluster interspike intervals between 10 and 25 ms were recorded from cells on the side of seizure onset. Because clustered action potential discharge is a normal pattern of firing for cells that discharge endogenous bursts, the relative decrease in proportions of 10-25 ms clustered interspike intervals occurring in the temporal lobe initiating seizures might reflect a reduction in endogenous burst discharges from that side. Reduced endogenous bursting could be due to the loss of burst discharging neurons as a product of seizure-related excitotoxicity. The identification of decreased interictal single neuronal burst discharge in epileptogenic structures stresses the difference between the interictal and ictal states in patients with complex partial seizures, and the importance of the transition between those states.

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Year:  1996        PMID: 8782868     DOI: 10.1016/0006-8993(96)00107-2

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  8 in total

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2.  Gray matter loss correlates with mesial temporal lobe neuronal hyperexcitability inside the human seizure-onset zone.

Authors:  Richard J Staba; Arne D Ekstrom; Nanthia A Suthana; Alison Burggren; Itzhak Fried; Jerome Engel; Susan Y Bookheimer
Journal:  Epilepsia       Date:  2011-11-29       Impact factor: 5.864

3.  Sleep states differentiate single neuron activity recorded from human epileptic hippocampus, entorhinal cortex, and subiculum.

Authors:  Richard J Staba; Charles L Wilson; Anatol Bragin; Itzhak Fried; Jerome Engel
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Review 4.  Electrophysiological biomarkers of epilepsy.

Authors:  Richard J Staba; Matt Stead; Gregory A Worrell
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Review 5.  What is the importance of abnormal "background" activity in seizure generation?

Authors:  Richard J Staba; Gregory A Worrell
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Review 6.  Mechanisms of physiological and epileptic HFO generation.

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7.  In vivo neuronal firing patterns during human epileptiform discharges replicated by electrical stimulation.

Authors:  Gonzalo Alarcón; Juan Martinez; Shashivadan V Kerai; Maria E Lacruz; Rodrigo Quian Quiroga; Richard P Selway; Mark P Richardson; Jorge J García Seoane; Antonio Valentín
Journal:  Clin Neurophysiol       Date:  2012-03-11       Impact factor: 3.708

8.  A Purinergic P2 Receptor Family-Mediated Increase in Thrombospondin-1 Bolsters Synaptic Density and Epileptic Seizure Activity in the Amygdala-Kindling Rat Model.

Authors:  Hongliu Sun; Luyu Ma; Yurong Zhang; Xiaohong Pan; Chaoyun Wang; Jinjin Zhang; Xiuli Zhang; Hongwei Sun; Qiaoyun Wang; Wei Zhu
Journal:  Front Cell Neurosci       Date:  2018-10-01       Impact factor: 5.505

  8 in total

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