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西格玛-1受体与神经元兴奋性

Sigma-1 Receptor and Neuronal Excitability.

作者信息

Kourrich Saïd

机构信息

Department of Psychiatry, University of Texas Southwestern Medical Center, 2201 Inwood Road, Dallas, TX, 75390-9070, USA.

出版信息

Handb Exp Pharmacol. 2017;244:109-130. doi: 10.1007/164_2017_8.

Abstract

The sigma-1 receptor (Sig-1R), via interaction with various proteins, including voltage-gated and ligand-gated ion channels (VGICs and LGICs), is involved in a plethora of neuronal functions. This capability to regulate a variety of ion channel targets endows the Sig-1R with a powerful capability to fine tune neuronal excitability, and thereby the transmission of information within brain circuits. This versatility may also explain why the Sig-1R is associated to numerous diseases at both peripheral and central levels. To date, how the Sig-1R chooses its targets and how the combinations of target modulations alter overall neuronal excitability is one of the challenges in the field of Sig-1R-dependent regulation of neuronal activity. Here, we will describe and discuss the latest findings on Sig-1R-dependent modulation of VGICs and LGICs, and provide hypotheses that may explain the diverse excitability outcomes that have been reported so far.

摘要

σ-1受体(Sig-1R)通过与包括电压门控离子通道和配体门控离子通道(VGICs和LGICs)在内的多种蛋白质相互作用,参与了众多神经元功能。这种调节多种离子通道靶点的能力赋予了Sig-1R强大的精细调节神经元兴奋性的能力,从而影响脑回路内信息的传递。这种多功能性也可以解释为什么Sig-1R在周围和中枢水平都与多种疾病相关。迄今为止,Sig-1R如何选择其靶点以及靶点调节的组合如何改变整体神经元兴奋性,是Sig-1R依赖性神经元活动调节领域的挑战之一。在此,我们将描述和讨论关于Sig-1R依赖性VGICs和LGICs调节的最新发现,并提出一些假说,以解释迄今为止报道的各种兴奋性结果。

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