d-安非他明诱发蜗牛中央神经元动作电位的突然放电:抗惊厥药的作用

Yi-Hung Chen , Cheng-Hsuan Chang , Gow-Jaw Liang , Shiang-Suo Huang , Hung-Ming Hsieh , Chen-Ming Teng , Ming-Cheng Tsai
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引用次数: 5

摘要

以鉴定的非洲蜗牛(Achatina fulica Ferussac) RP4神经元为实验对象,研究了抗惊厥药物对d-安非他明诱发的蜗牛中枢神经元动作电位爆发的影响。d-安非他明可引起膜电位振荡和动作电位爆发,并呈浓度依赖性。电压箝位研究表明,d-安非他明在- 40 ~ - 10 mV的稳态I-V曲线上产生负斜率电阻(NSR)。细胞外应用苯妥英可减轻动作电位的突发放电,但对乙氧亚胺、卡马西平和丙戊酸没有影响。苯妥英阻断了d-安非他明引起的非甾体受体反应。然而,如果添加卡马西平,NSR不会改变。上述结果表明,在4种抗惊厥药中,只有苯妥英能减轻d-安非他命引起的蜗牛神经元动作电位的突然放电。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Burst firing of action potentials in central snail neurons elicited by d-amphetamine: effect of anticonvulsants

The effect of anticonvulsants on the burst firing of action potentials in snail central neuron elicited by d-amphetamine was studied in the identified RP4 neuron of the African snail, Achatina fulica Ferussac. Oscillation of membrane potential and burst firing of action potentials were elicited by d-amphetamine in a concentration-dependent manner. Voltage clamped studies revealed that d-amphetamine elicited a negative slope resistance (NSR) in steady-state IV curve between −40 and −10 mV. The burst firing of action potentials was alleviated following extracellular application of phenytoin, but was not affected after ethosuximide, carbamazepine, and valproic acid. The NSR elicited by d-amphetamine was blocked by phenytoin. However, the NSR was not altered if carbamazepine was added. These results suggest that of the four anticonvulsants tested, only phenytoin could alleviate the burst firing of action potentials elicited by d-amphetamine in snail neuron.

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