[Regulation of the activity of monoaminergic neurons by ion channels: an opportunity for new therapeutic approaches?].

V Seutin
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引用次数: 0

Abstract

Small-conductance ca2+ -activated potassium (SK) channels underlie one component of the afterhyperpolarization which follows one or several action potentials in neurons. Their blockade enhances neuronal excitability and, in some cases, produces a significant depolarization within dendrites. Three subtypes of SK subunits exist and are differentially expressed in the brain. We have developed SK channel blockers, we have characterized their potency and have used some of them as pharmacological tools. Moreover, we have shown that SK channel blockade increases dopaminergic and serotonergic, but not noradrenergic transmission. We believe that this is an original way of modulating brain function. Our next goal is to find subtype-selective blockers, using a variety of approaches, including molecular modelling.

[通过离子通道调节单胺能神经元的活动:新治疗方法的机会?]。
小电导ca2+活化钾(SK)通道是后超极化的一个组成部分,它遵循神经元中的一个或几个动作电位。它们的阻断增强了神经元的兴奋性,在某些情况下,在树突内产生显著的去极化。SK亚基存在三种亚型,并在大脑中有差异表达。我们已经开发了SK通道阻滞剂,我们已经描述了它们的效力,并将它们中的一些用作药理工具。此外,我们已经表明SK通道阻断增加多巴胺能和血清素能,但不增加去甲肾上腺素能的传递。我们相信这是调节大脑功能的一种原始方式。我们的下一个目标是找到亚型选择性阻滞剂,使用各种方法,包括分子建模。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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