» Articles » PMID: 38123150

The Concise Guide to PHARMACOLOGY 2023/24: Ion Channels

Abstract

The Concise Guide to PHARMACOLOGY 2023/24 is the sixth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of approximately 1800 drug targets, and over 6000 interactions with about 3900 ligands. There is an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (https://www.guidetopharmacology.org/), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes almost 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/10.1111/bph.16178. Ion channels are one of the six major pharmacological targets into which the Guide is divided, with the others being: G protein-coupled receptors, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2023, and supersedes data presented in the 2021/22, 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.

Citing Articles

Targeting Kv7 Potassium Channels for Epilepsy.

Perucca E, Taglialatela M CNS Drugs. 2025; 39(3):263-288.

PMID: 39853501 PMC: 11850491. DOI: 10.1007/s40263-024-01155-3.


In Vitro Hepatic Metabolism Input Parameters Support Toxicokinetic Simulations for the Formation of Methoxy Propionic Acid From β-Isomer Propylene Glycol Methyl Ether.

Werner S, Hegg L, Hopf N, Borgatta M, Suter-Dick L Pharmacol Res Perspect. 2024; 12(6):e70037.

PMID: 39655648 PMC: 11629119. DOI: 10.1002/prp2.70037.


NMDA Receptor-Mediated Ca Flux Attenuated by the NMDA Receptor/TRPM4 Interface Inhibitor Brophenexin.

Casby J, Gansemer B, Thayer S Pharmacol Res Perspect. 2024; 12(6):e70038.

PMID: 39574295 PMC: 11582383. DOI: 10.1002/prp2.70038.


Incidence and trend of cardiac events among children and young adults exposed to psychopharmacological treatment (2006-2018): A nationwide register-based study.

Elmowafi H, Kindblom J, Halldner L, Gyllenberg D, Naumburg E Br J Clin Pharmacol. 2024; 91(3):817-828.

PMID: 39448545 PMC: 11862795. DOI: 10.1111/bcp.16321.


Chronic ethanol exposure in mice evokes pre- and postsynaptic deficits in GABAergic transmission in ventral tegmental area GABA neurons.

Mitten E, Souders A, Marron Fernandez de Velasco E, Aguado C, Lujan R, Wickman K Br J Pharmacol. 2024; 182(1):69-86.

PMID: 39358985 PMC: 11831720. DOI: 10.1111/bph.17335.


References
1.
Hackos D, Hanson J . Diverse modes of NMDA receptor positive allosteric modulation: Mechanisms and consequences. Neuropharmacology. 2016; 112(Pt A):34-45. DOI: 10.1016/j.neuropharm.2016.07.037. View

2.
Cochet-Bissuel M, Lory P, Monteil A . The sodium leak channel, NALCN, in health and disease. Front Cell Neurosci. 2014; 8:132. PMC: 4033012. DOI: 10.3389/fncel.2014.00132. View

3.
Clapham D, Garbers D . International Union of Pharmacology. L. Nomenclature and structure-function relationships of CatSper and two-pore channels. Pharmacol Rev. 2005; 57(4):451-4. DOI: 10.1124/pr.57.4.7. View

4.
Di Virgilio F, Schmalzing G, Markwardt F . The Elusive P2X7 Macropore. Trends Cell Biol. 2018; 28(5):392-404. DOI: 10.1016/j.tcb.2018.01.005. View

5.
Lochner M, Thompson A . A review of fluorescent ligands for studying 5-HT3 receptors. Neuropharmacology. 2015; 98:31-40. DOI: 10.1016/j.neuropharm.2015.04.002. View