Multiple actions of the novel anticonvulsant drug topiramate in the rat subiculum in vitro

被引:26
作者
Kawasaki, H
Tancredi, V
D'Arcangelo, G
Avoli, M
机构
[1] McGill Univ, Montreal Neurol Inst, Res Grp Cell Biol Excitable Tissues, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Dept Physiol, Montreal, PQ H3A 2B4, Canada
[4] Univ Roma Tor Vergata, Dipartimento Neurosci, I-00173 Rome, Italy
基金
英国医学研究理事会;
关键词
subiculum; topiramate; Na+-electrogenesis; GABA; rat;
D O I
10.1016/S0006-8993(98)00785-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We used an in vitro slice preparation to study whether and how the anticonvulsant drug topiramate (TPM, 50-500 mu M) modulates the excitability of rat subicular neurons that generate action potential bursts mainly caused by voltage-dependent, Na+-electrogenesis. Subiculum is a gating structure for outputs originating from the hippocampus proper, and thus it may play a role in limbic seizures. In 28/45 neurons, TPM induced a steady hyperpolarization of the resting membrane potential (RMP) that ranged between -2 and -16 mV and was associated with a 24-62% decrease of the apparent membrane input resistance. TPM also depressed the ability of these cells to generate action potential bursts in response to brief (5-150 ms) depolarizing pulses, such an effect was characterized by an increase in the amount of intracellular depolarizing current required for eliciting action potential bursts, and it also occurred when the TPM-induced steady hyperpolarization was compensated by injecting steady depolarizing current. In addition TPM reduced by approx. 50% the regular action potential firing elicited by prolonged (350-1000 ms) depolarizing pulses (n = 15 of 27 neurons). Recovery of the TPM-induced changes was not seen during washout for periods of 20-80 min (n = 7). Both the steady hyperpolarization of the RMP and the input resistance decrease elicited by TPM were markedly reduced by the GABA(A) receptor antagonists bicuculline methiodide (10 mu M; n = 6) or picrotoxin (100 mu M; n = 2); such an effect was associated with a reduction, but not with blockade of the depressant action exerted by TPM on burst generation. Our findings indicate that TPM reduces subicular cell excitability, and modifies bursting ability and repetitive firing properties. These effects may be ascribed to actions on voltage-gated, Na+ electrogenesis and GABA(A) receptors. We propose that these changes in excitability may all contribute to the anticonvulsant action of TPM in limbic seizures that occur in temporal lobe epilepsy patients. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:125 / 134
页数:10
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