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阿米替林对上皮钠通道的传导特性具有双重作用。

Amitriptyline has a dual effect on the conductive properties of the epithelial Na channel.

作者信息

Pena Florentina, Neaga Emil, Amuzescu Bogdan, Nitu Alina, Flonta Maria-Luisa

机构信息

Department of Animal Physiology and Biophysics, University of Bucharest, Faculty of Biology, Splaiul Independentei 91-95, Bucharest R-76201, Romania.

出版信息

J Pharm Pharmacol. 2002 Oct;54(10):1393-8. doi: 10.1211/002235702760345482.

Abstract

This study was undertaken with the aim of testing the action of amitriptyline on the epithelial Na channel (ENaC), which belongs to the same family (Deg/ENaC) as ASICs (acid-sensing ion channels) and many other putative members in the brain. We assumed that, having a common protein structure, characterization of the amitriptyline-ENaC interaction could help to elucidate the analgesic mechanism of this tricyclic antidepressant. Na-channel characteristics were derived from the analysis of blocker-induced lorentzian noise produced by amiloride. The effect of amitriptyline, present in the mucosal bathing solution, on the transepithelial short-circuit current (I(sc)) and conductance (G(t)), and on the blocker-induced noise of apical Na channels, was studied on isolated ventral skin of the frog Rana ridibunda. Amitriptyline exerted a dual effect on the macroscopic short-circuit current and conductance of the epithelia, increasing these two parameters in the concentration range 0.1-50 microM, while at higher concentrations (100-1000 microM) it showed an inhibitory action. The decrease in the association rate (k(01)) of amiloride to the apical Na channels from 15.6+/-4.2 microM(-1) s(-1) in control Cl-Ringer to 7.4+/-1.7 microM(-1) s(-1) at 200 microM amitriptyline in a concentration-dependent manner suggests a competitive binding of amitriptyline to the pyrazine ring binding site for amiloride.

摘要

本研究旨在测试阿米替林对上皮钠通道(ENaC)的作用,该通道与酸敏感离子通道(ASICs)以及大脑中许多其他假定成员属于同一家族(Deg/ENaC)。我们假设,由于具有共同的蛋白质结构,对阿米替林与ENaC相互作用的表征有助于阐明这种三环类抗抑郁药的镇痛机制。钠通道特性来自对氨氯地平产生的阻滞剂诱导的洛伦兹噪声的分析。在青蛙泽蛙的离体腹侧皮肤中,研究了存在于黏膜浴液中的阿米替林对跨上皮短路电流(I(sc))和电导(G(t))以及对顶端钠通道的阻滞剂诱导噪声的影响。阿米替林对上皮的宏观短路电流和电导产生双重作用,在0.1 - 50 microM的浓度范围内增加这两个参数,而在较高浓度(100 - 1000 microM)时则表现出抑制作用。氨氯地平与顶端钠通道的结合速率(k(01))从对照Cl - 林格液中的15.6±4.2 microM(-1) s(-1)以浓度依赖性方式降低至200 microM阿米替林时的7.4±1.7 microM(-1) s(-1),这表明阿米替林与氨氯地平的吡嗪环结合位点存在竞争性结合。

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