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益智药长春西汀对延迟整流钾电流的阻断作用比对高阈值钙电流的阻断作用更强。

Nootropic agent vinpocetine blocks delayed rectified potassium currents more strongly than high-threshold calcium currents.

作者信息

Solntseva E I

机构信息

Science Research Institute of the Brain, Russian Academy, Medical Sciences, Moscow.

出版信息

Neurosci Behav Physiol. 1998 Mar-Apr;28(2):116-20. doi: 10.1007/BF02461956.

DOI:10.1007/BF02461956
PMID:9604212
Abstract

A two-microelectrode potential clamping method was used on isolated common snail neurons to measure high-threshold Ca2+ and delayed rectified K+ currents. Addition of the nootropic agent vinpocetine (VPC) to the bathing solution rapidly and reversibly inhibited both types of current. The effects of VPC were dose-dependent and were independent of the test stimulus voltage. Maximum blockade of the Ca2+ current averaged 27% at a VPC concentration of 600 microM. Maximum blockade of the K+ current averaged 76% at a VPC concentration of 30 microM. It is concluded that K+ channels are more likely targets of VPC than Ca2+ channels.

摘要

采用双微电极电压钳制方法,在分离的普通蜗牛神经元上测量高阈值Ca2+电流和延迟整流K+电流。向浴液中添加促智药长春西汀(VPC)可快速且可逆地抑制这两种电流。VPC的作用呈剂量依赖性,且与测试刺激电压无关。在VPC浓度为600 microM时,Ca2+电流的最大阻断平均为27%。在VPC浓度为30 microM时,K+电流的最大阻断平均为76%。得出的结论是,与Ca2+通道相比,K+通道更可能是VPC的作用靶点。

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Neurosci Behav Physiol. 1998 Mar-Apr;28(2):116-20. doi: 10.1007/BF02461956.
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本文引用的文献

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9-Amino-1,2,3,4-tetrahydroacridine (THA), an alleged drug for the treatment of Alzheimer's disease, inhibits acetylcholinesterase activity and slow outward K+ current.9-氨基-1,2,3,4-四氢吖啶(THA),一种据称可用于治疗阿尔茨海默病的药物,可抑制乙酰胆碱酯酶活性并减慢外向钾电流。
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