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COX-2抑制剂对幼鼠海马CA1区锥体神经元钠通道的影响
引用本文:张海菊,姚宝珍,凌伟. COX-2抑制剂对幼鼠海马CA1区锥体神经元钠通道的影响[J]. 临床神经电生理学杂志, 2012, 21(3): 129-134,148
作者姓名:张海菊  姚宝珍  凌伟
作者单位:武汉大学人民医院儿科,湖北武汉,430063
基金项目:本研究为武汉大学青年教师资助项目(编号:111171)
摘    要:目的:研究环氧合酶-2(cyclooxygenase-2,COX-2)抑制剂硝基苯一甲磺酸(NS398)对大鼠海马CAl区锥体神经元电压依赖性钠通道的影响,以及在幼鼠痫性发作中的作用。方法:出生后14d龄SD大鼠制作海马组织脑切片,脑片灌流液中灌流不同浓度NS-398,全细胞记录在阶跃模式(episod—ic)中,通过相应的刺激方案(protocol),记录对电压依赖性钠通道电流密度及幅度的影响,观察对钠通道激活及失活曲线的影响。结果:①加入20μMol/L(μM)NS-398能明显抑制电流密度,而且在最大激活电位时抑制最明显(P〈O.01),抑制呈电压依赖性,但是不能改变其最大激活电位;②加入20μmol/LNS-398不能明显改变钠通道的电压依赖性激活状态(P〉0.05);③加入20Fmol/LNS-398,电压依赖性钠失活电流的失活曲线明显向负极化方向移动(左移5.2mV,P〈0.05);④相同指令电压的刺激下,加入NS-398组的1/Lmax比正常组减小,NS-398能明显延长电压依赖性钠电流的失活时间。结论:COX-2抑制剂能抑制大鼠海马脑片CAl区锥体神经元电压依赖性钠通道,延长电压依赖性钠电流的失活时间;减少Na+电流,延缓动作电位的发放和传播,降低神经元的兴奋性。

关 键 词:癫痫  坏氧合酶-2(COX-2)抑制剂  钠离子通道  全细胞记录

The effects of COX-2 inhibitor on voltage-dependent sodium channel in hippocampal CA1 pyramidal neuron in immature rats
ZHANG Haiju , YAO Baozhen , LING Wei. The effects of COX-2 inhibitor on voltage-dependent sodium channel in hippocampal CA1 pyramidal neuron in immature rats[J]. Journal of Clinical Electroneurophysiology, 2012, 21(3): 129-134,148
Authors:ZHANG Haiju    YAO Baozhen    LING Wei
Affiliation:Department of Pediatrics, Renmin Hospital of Wuhan University, Wuhan (430063), Hubei China
Abstract:Objective:To study the mechanism of COX-2 inhibitor in immature epileptic ratsby ob- serving the effects of COX-2 inhibitor on hippocampal pyramidal neuron in vitro hippocampal tissue epi- leptiform discharges and the alterations of synaptie activities. Methods.. Hippocampal slices were prepared from 2wk-old rats with for Sprague-Dawley (SD)whole-cell patch clamp recording. The hippocampal slice epileptic models were induced by dabbling penicillin into the slices. The alterations of the CA1 py- ramidal neurons electrophysiologica[ properties in epileptic rats after dabbling different concentration of COX-2 inhibitor (NS-398) into the slices were analyzed with whole cell recording technology. Results.. In the brain slices of penicillin-induced epileptic discharges Meanwhile NS -398 significantly enhanced the frequency and prolonged the decayed time of SLPSCs, but little impact on the current rate. Concluslon: The impact of NS-398 occurred in the voltage-dependent sodium current: NS -398 can reduce the current rate and extent the no-answer period of the voltage-dependent sodium channel to decreaseg the open frequency of sodium channel by extending inactivation recovery phase from deactivation,and neuronal action potential frequency of issuance corresponding declined;
Keywords:Epilepsy  COX-2 inhibitor  Voltage-dependent sodium channel  Whole cell recording
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