Antiepileptic drugs abolish ictal but not interictal epileptiform discharges in vitro

被引:67
作者
D'Antuono, Margherita [1 ,2 ,3 ]
Koehling, Ruediger [4 ]
Ricalzone, Serena [1 ,2 ,3 ]
Gotman, Jean [1 ,2 ,3 ]
Biagini, Giuseppe [5 ]
Avoli, Massimo [1 ,2 ,3 ,6 ]
机构
[1] McGill Univ, Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Dept Neurol, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Dept Neurosurg, Montreal, PQ H3A 2B4, Canada
[4] Univ Rostock, Inst Physiol, Rostock, Germany
[5] Univ Modena & Reggio Emilia, Dipartimento Sci Biomed, Modena, Italy
[6] Univ Roma La Sapienza, Dipartimento Med Sperimentale, I-00185 Rome, Italy
基金
加拿大健康研究院;
关键词
Antiepileptic drugs; 4-Aminopyridine; Entorhinal Cortex; Epilepsy; Hippocampus; Picrotoxin; GABA-MEDIATED POTENTIALS; TEMPORAL-LOBE EPILEPSY; RAT HIPPOCAMPAL SLICES; ENTORHINAL CORTEX; LOW MAGNESIUM; CEREBROSPINAL-FLUID; LIMBIC SEIZURES; ANTICONVULSANTS; SYNCHRONIZATION; 4-AMINOPYRIDINE;
D O I
10.1111/j.1528-1167.2009.02273.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
P>Purpose: We established the effects of the antiepileptic drugs (AEDs) carbamazepine (CBZ), topiramate (TPM), and valproic acid (VPA) on the epileptiform activity induced by 4-aminopyridine (4AP) in the rat entorhinal cortex (EC) in an in vitro brain slice preparation. Methods: Brain slices were obtained from Sprague-Dawley rats (200-250 g). Field and intracellular recordings were made from the EC during bath application of 4AP (50 mu m). AEDs, and in some experiments, picrotoxin were bath applied concomitantly. Results: Prolonged (> 3 s), ictal-like epileptiform events were abolished by CBZ (50 mu m), TPM (50 mu m), and VPA (1 mm), whereas shorter (< 3 s) interictal-like discharges continued to occur, even at concentrations up to 4-fold as high. gamma-Aminobutyric acid (GABA)(A)-receptor antagonism changed the 4AP-induced activity into recurrent interictal-like events that were not affected by CBZ or TPM, even at the highest concentrations. To establish whether these findings reflected the temporal features of the epileptiform discharges, we tested CBZ and TPM on 4AP-induced epileptiform activity driven by stimuli delivered at 100-, 10-, and 5-s intervals; these AEDs reduced ictal-like responses to stimuli at 100-s intervals at nearly therapeutic concentrations, but did not influence shorter interictal-like events elicited by stimuli delivered every 10 or 5 s. Conclusions: We conclude that the AED ability to control epileptiform synchronization in vitro depends mainly on activity-dependent characteristics such as discharge duration. Our data are in keeping with clinical evidence indicating that interictal activity is unaffected by AED levels that are effective to stop seizures.
引用
收藏
页码:423 / 431
页数:9
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