Ontology type: schema:ScholarlyArticle
1986-02
AUTHORS ABSTRACTIn cardiac muscle the exchange of intracellular Ca2+ for extracellular Na+ is an important transport mechanism for regulation of the intracellular free Ca2+ concentration ([Ca]i) and hence the contractile strength of the heart (ref. 1 ; for reviews see refs 2–4). Due to its stoichiometry of ≥3:l Na+/Ca2+ (refs 3,5), Na-Ca exchange is supposed to generate a current across the cell membrane. It is thought that such a current may contribute to cardiac action potential and physiological or pathological pacemaker activity6,7. Although the occurrence of Na-Ca exchange is well documented, a membrane current generated by this transport has not been identified unequivocally. Previous attempts to detect such a current-in multicellular preparations, for example, by measuring small current differences after varying the extracellular ionic composition8, although providing evidence, did not rule out other possible interpretations. Here we demonstrate that a transient rise in [Ca]i caused by release of Ca from sarcoplasmic reticulum (SR) generates a membrane current in cardiac myocytes. The dependence of this current on the transmembrane gradients for Na+ and Ca2+ and on membrane potential meets the criteria for a current produced by electrogenic Na-Ca exchange. Cyclic activation of this current by release of Ca from the SR can cause maintained spontaneous activity, suggesting that Na-Ca exchange contributes to certain forms of cardiac pacemaking. More... »
PAGES597-599
http://scigraph.springernature.com/pub.10.1038/319597a0
DOIhttp://dx.doi.org/10.1038/319597a0
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PUBMEDhttps://www.ncbi.nlm.nih.gov/pubmed/2418367
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