IUPHAR/BPS Guide to Pharmacology CITE
https://doi.org/10.2218/gtopdb/F180/2019.4
SLC8 family of sodium/calcium exchangers (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
Jules Hancox1
- University of Bristol, UK
Abstract
The sodium/calcium exchangers (NCX) use the extracellular sodium concentration to facilitate the extrusion of calcium out of the cell. Alongside the plasma membrane Ca2+-ATPase (PMCA) and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase (SERCA), as well as the sodium/potassium/calcium exchangers (NKCX, SLC24 family), NCX allow recovery of intracellular calcium back to basal levels after cellular stimulation. When intracellular sodium ion levels rise, for example, following depolarisation, these transporters can operate in the reverse direction to allow calcium influx and sodium efflux, as an electrogenic mechanism. Structural modelling suggests the presence of 9 TM segments, with a large intracellular loop between the fifth and sixth TM segments.
Contents
This is a citation summary for SLC8 family of sodium/calcium exchangers in the
Guide to Pharmacology
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Database links
SLC8 family of sodium/calcium exchangers
http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=180
Transporters
NCX1(Sodium/calcium exchanger 1)
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=945
NCX2(Sodium/calcium exchanger 2)
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=946
NCX3(Sodium/calcium exchanger 3)
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=947
References
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- Iwamoto T and Kita S. (2006) YM-244769, a novel Na+/Ca2+ exchange inhibitor that preferentially inhibits NCX3, efficiently protects against hypoxia/reoxygenation-induced SH-SY5Y neuronal cell damage. Mol. Pharmacol. 70: 2075-83 [PMID:16973719]
- Jost N, Nagy N, Corici C, Kohajda Z, Horváth A, Acsai K, Biliczki P, Levijoki J, Pollesello P and Koskelainen T et al.. (2013) ORM-10103, a novel specific inhibitor of the Na+/Ca2+ exchanger, decreases early and delayed afterdepolarizations in the canine heart. Br. J. Pharmacol. 170: 768-78 [PMID:23647096]
- Secondo A, Pignataro G, Ambrosino P, Pannaccione A, Molinaro P, Boscia F, Cantile M, Cuomo O, Esposito A and Sisalli MJ et al.. (2015) Pharmacological characterization of the newly synthesized 5-amino-N-butyl-2-(4-ethoxyphenoxy)-benzamide hydrochloride (BED) as a potent NCX3 inhibitor that worsens anoxic injury in cortical neurons, organotypic hippocampal cultures, and ischemic brain. ACS Chem Neurosci 6: 1361-70 [PMID:25942323]
- Yamashita K, Watanabe Y, Kita S, Iwamoto T and Kimura J. (2016) Inhibitory effect of YM-244769, a novel Na+/Ca2+ exchanger inhibitor on Na+/Ca2+ exchange current in guinea pig cardiac ventricular myocytes. Naunyn Schmiedebergs Arch. Pharmacol. 389: 1205-1214 [PMID:27480939]