Effects of Topiramate on Sustained Repetitive Firing and Spontaneous Recurrent Seizure Discharges in Cultured Hippocampal Neurons

Purpose: In this study, we examined the effects of topiramate (TPM) on the electrophysiologic properties of cultured rat hippocampal pyramidal neurons. Methods: Whole‐cell current‐clamp recording techniques were used to determine the effects of TPM on sustained repetitive firing (SRF), spontaneous e...

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Veröffentlicht in:Epilepsia (Copenhagen) 2000-01, Vol.41 (s1), p.40-44
Hauptverfasser: DeLorenzo, Robert J., Sombati, Sompong, Coulter, Douglas A.
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Sprache:eng
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Zusammenfassung:Purpose: In this study, we examined the effects of topiramate (TPM) on the electrophysiologic properties of cultured rat hippocampal pyramidal neurons. Methods: Whole‐cell current‐clamp recording techniques were used to determine the effects of TPM on sustained repetitive firing (SRF), spontaneous epileptiform‐burst firing, and spontaneous recurrent seizures (SRS). Results: Topiramate at therapeutic concentrations (10–100 μM) significantly decreased or abolished SRF in a dose‐dependent and partially reversible manner. When transiently exposed to a medium in which Mg2+ is omitted, hippocampal neurons in culture develop SRS (“epilepsy”) and epileptiform discharges. Application of TPM at concentrations ranging from 10 to 100 μM to cells displaying seizure activity caused a concentration‐dependent decrease in the number of action potentials within a burst and in the average duration of epileptiform activity. Both effects were partially reversed during a 5‐ to 30‐min drug washout period. Conclusions: These effects on the electrophysiologic properties of cultured neurons are consistent with the concept that TPM exerts modulatory effects on voltage‐dependent Na+ and/ or Ca2+ conductances responsible for the generation and propagation of action potentials. Topiramate also may inhibit synaptic conductances responsible for transmission of epileptiform discharges.
ISSN:0013-9580
1528-1167
DOI:10.1111/j.1528-1157.2000.tb02170.x