Antiarrhythmic and Inotropic Effects of Selective Na+/Ca2+ Exchanger Inhibition What Can We Learn from the Pharmacological Studies? /

Life-long stable heart function requires a critical balance of intracellular Ca2+. Several ion channels and pumps cooperate in a complex machinery that controls the influx, release, and efflux of Ca2+. Probably one of the most interesting and most complex players of this crosstalk is the Na+/Ca2+ ex...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Nagy Norbert
Tóth Noémi
Nánási Péter Pál
Dokumentumtípus: Cikk
Megjelent: 2022
Sorozat:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 23 No. 23
Tárgyszavak:
doi:10.3390/ijms232314651

mtmt:33271845
Online Access:http://publicatio.bibl.u-szeged.hu/25672
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520 3 |a Life-long stable heart function requires a critical balance of intracellular Ca2+. Several ion channels and pumps cooperate in a complex machinery that controls the influx, release, and efflux of Ca2+. Probably one of the most interesting and most complex players of this crosstalk is the Na+/Ca2+ exchanger, which represents the main Ca2+ efflux mechanism; however, under some circumstances, it can also bring Ca2+ into the cell. Therefore, the inhibition of the Na+/Ca2+ exchanger has emerged as one of the most promising possible pharmacological targets to increase Ca2+ levels, to decrease arrhythmogenic depolarizations, and to reduce excessive Ca2+ influx. In line with this, as a response to increasing demand, several more or less selective Na+/Ca2+ exchanger inhibitor compounds have been developed. In the past 20 years, several results have been published regarding the effect of Na+/Ca2+ exchanger inhibition under various circumstances, e.g., species, inhibitor compounds, and experimental conditions; however, the results are often controversial. Does selective Na+/Ca2+ exchanger inhibition have any future in clinical pharmacological practice? In this review, the experimental results of Na+/Ca2+ exchanger inhibition are summarized focusing on the data obtained by novel highly selective inhibitors. 
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