Early Deficits in Spatial Memory and Theta Rhythm in Experimental Temporal Lobe Epilepsy

Patients with temporal lobe epilepsy (TLE), the most common form of epilepsy in adults, often display cognitive deficits. The time course and underlying mechanisms of cognitive decline remain unknown during epileptogenesis (the process leading to epilepsy). Using the rat pilocarpine model of TLE, we...

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Veröffentlicht in:The Journal of neuroscience 2009-04, Vol.29 (17), p.5402-5410
Hauptverfasser: Chauviere, Laetitia, Rafrafi, Nadia, Thinus-Blanc, Catherine, Bartolomei, Fabrice, Esclapez, Monique, Bernard, Christophe
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container_issue 17
container_start_page 5402
container_title The Journal of neuroscience
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creator Chauviere, Laetitia
Rafrafi, Nadia
Thinus-Blanc, Catherine
Bartolomei, Fabrice
Esclapez, Monique
Bernard, Christophe
description Patients with temporal lobe epilepsy (TLE), the most common form of epilepsy in adults, often display cognitive deficits. The time course and underlying mechanisms of cognitive decline remain unknown during epileptogenesis (the process leading to epilepsy). Using the rat pilocarpine model of TLE, we performed a longitudinal study to assess spatial and nonspatial cognitive performance during epileptogenesis. In parallel, we monitored interictal-like activity (ILA) in the hippocampal CA1 region, as well as theta oscillations, a brain rhythm central to numerous cognitive processes. Here, we report that spatial memory was altered soon after pilocarpine-induced status epilepticus, i.e., already during the seizure-free, latent period. Spatial deficits correlated with a decrease in the power of theta oscillations but not with the frequency of ILA. Spatial deficits persisted when animals had spontaneous seizures (chronic stage) without further modification. In contrast, nonspatial memory performances remained unaffected throughout. We conclude that the reorganization of hippocampal circuitry that immediately follows the initial insult can affect theta oscillation mechanisms, in turn, resulting in deficits in hippocampus-dependent memory tasks. These deficits may be dissociated from the process that leads to epilepsy itself but could instead constitute, as ILA, early markers in at-risk patients and/or provide beneficial therapeutic targets.
doi_str_mv 10.1523/JNEUROSCI.4699-08.2009
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The time course and underlying mechanisms of cognitive decline remain unknown during epileptogenesis (the process leading to epilepsy). Using the rat pilocarpine model of TLE, we performed a longitudinal study to assess spatial and nonspatial cognitive performance during epileptogenesis. In parallel, we monitored interictal-like activity (ILA) in the hippocampal CA1 region, as well as theta oscillations, a brain rhythm central to numerous cognitive processes. Here, we report that spatial memory was altered soon after pilocarpine-induced status epilepticus, i.e., already during the seizure-free, latent period. Spatial deficits correlated with a decrease in the power of theta oscillations but not with the frequency of ILA. Spatial deficits persisted when animals had spontaneous seizures (chronic stage) without further modification. In contrast, nonspatial memory performances remained unaffected throughout. We conclude that the reorganization of hippocampal circuitry that immediately follows the initial insult can affect theta oscillation mechanisms, in turn, resulting in deficits in hippocampus-dependent memory tasks. 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subjects Animals
Cognitive science
Epilepsy, Temporal Lobe - chemically induced
Epilepsy, Temporal Lobe - physiopathology
Male
Memory - physiology
Memory Disorders - chemically induced
Memory Disorders - physiopathology
Pilocarpine - toxicity
Psychology
Rats
Rats, Wistar
Spatial Behavior - drug effects
Spatial Behavior - physiology
Theta Rhythm - drug effects
Time Factors
title Early Deficits in Spatial Memory and Theta Rhythm in Experimental Temporal Lobe Epilepsy
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