Golumbek P T, Rho J M, Spain W J, van Brederode J F M
Department of Neurology, University of Washington School of Medicine, Seattle, WA, USA.
Naunyn Schmiedebergs Arch Pharmacol. 2004 Sep;370(3):176-82. doi: 10.1007/s00210-004-0968-8. Epub 2004 Sep 1.
Flunarizine, a non-selective blocker of voltage-dependent Ca(2+) and Na(+) channels, is clinically effective against several neurological disorders, including epilepsy, migraine, and alternating hemiplegia of childhood. We examined the effects of flunarizine on spontaneous post-synaptic currents in acute brain slices maintained in vitro using patch-clamp electrophysiology. Flunarizine significantly attenuated the amplitude of spontaneous currents in pyramidal neurons from juvenile rat neocortex. Flunarizine had no effect on miniature spontaneous events recorded in the presence of tetrodotoxin, a blocker of voltage-dependent sodium channels. In high (9 mM) extracellular potassium, flunarizine reduced the amplitude and frequency of the spontaneous currents. Additionally, dimethyl sulfoxide, the solvent used in our experiments, reduced the amplitude of spontaneous currents, but only in high extracellular potassium. Our data suggest that the clinical activity of flunarizine may in part be a consequence of reducing spontaneous synaptic currents in the neocortex, especially under conditions of heightened neuronal activity.
氟桂利嗪是一种电压依赖性钙通道和钠通道的非选择性阻滞剂,临床上对多种神经系统疾病有效,包括癫痫、偏头痛和儿童交替性偏瘫。我们使用膜片钳电生理学方法研究了氟桂利嗪对体外培养的急性脑片中自发突触后电流的影响。氟桂利嗪显著降低了幼年大鼠新皮质锥体神经元自发电流的幅度。氟桂利嗪对在电压依赖性钠通道阻滞剂河豚毒素存在下记录的微小自发事件没有影响。在高(9 mM)细胞外钾浓度下,氟桂利嗪降低了自发电流的幅度和频率。此外,我们实验中使用的溶剂二甲基亚砜仅在高细胞外钾浓度下降低了自发电流的幅度。我们的数据表明,氟桂利嗪的临床活性可能部分是减少新皮质自发突触电流的结果,尤其是在神经元活动增强的情况下。