| Literature DB >> 28275909 |
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.Entities:
Keywords: AMPA receptor; Auxiliary subunit; Calcium channels; Chaperone protein; Intrinsic excitability; NMDA receptor; Potassium channels; Sigma-1 receptor; Sodium channels; Voltage-gated ion channels
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Year: 2017 PMID: 28275909 DOI: 10.1007/164_2017_8
Source DB: PubMed Journal: Handb Exp Pharmacol ISSN: 0171-2004