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左乙拉西坦抑制大鼠海马切片锥体神经元中的高电压激活钙电流。

Levetiracetam inhibits the high-voltage-activated Ca(2+) current in pyramidal neurones of rat hippocampal slices.

作者信息

Niespodziany I, Klitgaard H, Margineanu D G

机构信息

UCB S.A. Pharma Sector, Preclinical CNS Research, B-1420, Braine-l'Alleud, Belgium.

出版信息

Neurosci Lett. 2001 Jun 22;306(1-2):5-8. doi: 10.1016/s0304-3940(01)01884-5.

Abstract

The effect of the new antiepileptic drug levetiracetam (LEV; KEPPRA) on the neuronal high-voltage-activated (HVA) Ca(2+) current was investigated on pyramidal neurones, visually identified in the CA1 area of rat hippocampal slices. Nystatin-perforated patch clamp recordings were made under experimental conditions designed to study HVA Ca(2+) currents. The HVA current, activated by steadily increasing voltage-ramps, was reversibly eliminated by Cd(2+) and depressed by either nimodipine, or omega-Conotoxin GVIA. After 30 min perfusion of the slices with LEV 32 microM, the current decayed to 55+/-9% (mean+/-SEM; n=9) of the initial value, which is significantly (P<0.05, two-tailed t-test) lower than the rundown to 84+/-10% in a control group (n=10) of neurones. The limited, but significant depression of the neuronal HVA Ca(2+) current, produced by LEV at a clinically relevant concentration, might contribute to the antiepileptic action of the drug.

摘要

在大鼠海马切片CA1区经视觉识别的锥体神经元上,研究了新型抗癫痫药物左乙拉西坦(LEV;开浦兰)对神经元高电压激活(HVA)Ca(2+)电流的影响。在旨在研究HVA Ca(2+)电流的实验条件下,进行了制霉菌素穿孔膜片钳记录。由逐渐增加的电压斜坡激活的HVA电流可被Cd(2+)可逆性消除,并被尼莫地平或ω-芋螺毒素GVIA抑制。在用32μM的LEV灌注切片30分钟后,电流衰减至初始值的55±9%(平均值±标准误;n=9),这显著(P<0.05,双侧t检验)低于对照组(n=10)神经元衰减至84±10%的水平。LEV在临床相关浓度下对神经元HVA Ca(2+)电流产生的有限但显著的抑制作用,可能有助于该药物的抗癫痫作用。

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