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Review
. 2019 Sep 15;20(18):4572.
doi: 10.3390/ijms20184572.

Noncanonical Ion Channel Behaviour in Pain

Affiliations
Review

Noncanonical Ion Channel Behaviour in Pain

Cosmin I Ciotu et al. Int J Mol Sci. .

Abstract

Ion channels contribute fundamental properties to cell membranes. Although highly diverse in conductivity, structure, location, and function, many of them can be regulated by common mechanisms, such as voltage or (de-)phosphorylation. Primarily considering ion channels involved in the nociceptive system, this review covers more novel and less known features. Accordingly, we outline noncanonical operation of voltage-gated sodium, potassium, transient receptor potential (TRP), and hyperpolarization-activated cyclic nucleotide (HCN)-gated channels. Noncanonical features discussed include properties as a memory for prior voltage and chemical exposure, alternative ion conduction pathways, cluster formation, and silent subunits. Complementary to this main focus, the intention is also to transfer knowledge between fields, which become inevitably more separate due to their size.

Keywords: HCN channel; TRP channel; drug development; pharmacology; potassium channel; sodium channel.

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Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Hille B. Ion Channels of Excitable Membranes. 3rd ed. Sinauer Associates; Sunderland, MA, USA: 2001.
    1. Catterall W.A. From Ionic Currents to Molecular Mechanisms: The Structure and Function of Voltage-Gated Sodium Channels. Neuron. 2000;26:13–25. doi: 10.1016/S0896-6273(00)81133-2. - DOI - PubMed
    1. Catterall W.A. International Union of Pharmacology. XLVII. Nomenclature and Structure-Function Relationships of Voltage-Gated Sodium Channels. Pharmacol. Rev. 2005;57:397–409. doi: 10.1124/pr.57.4.4. - DOI - PubMed
    1. Lampert A., O’Reilly A.O., Reeh P., Leffler A. Sodium channelopathies and pain. Pflugers Arch. 2010;460:249–263. doi: 10.1007/s00424-009-0779-3. - DOI - PubMed
    1. Emery E.C., Luiz A.P., Wood J.N. Nav1.7 and other voltage-gated sodium channels as drug targets for pain relief. Expert Opin Ther Targets. 2016;20:975–983. doi: 10.1517/14728222.2016.1162295. - DOI - PMC - PubMed