Sodium entry through tetrodotoxin-sensitive channels triggered calcium release from the sarcoplasmic reticulum via sodium-calcium exchange in isolated cardiac myocytes.
Isolated cardiac myocytes
Membrane depolarization
Release of calcium from cardiac sarcoplasmic reticulum
The role of sodium-calcium exchange at the sarcolemma in the release of calcium from cardiac sarcoplasmic reticulum was investigated in voltage-clamped, isolated cardiac myocytes. In the absence of calcium entry through voltage-dependent calcium channels, membrane depolarization elicited release of calcium from ryanodine-sensitive internal stores. This process was dependent on sodium entry through tetrodotoxin-sensitive sodium channels. Calcium release under these conditions was also dependent on extracellular calcium concentration, suggesting a calcium-induced trigger release mechanism that involves calcium entry into the cell by sodium-calcium exchange. This sodium current-induced calcium release mechanism may explain, in part, the positive inotropic effects of cardiac glycosides and the negative inotropic effects of a variety of antiarrhythmic drugs that interact with cardiac sodium channels. In response to a transient rise of intracellular sodium, sodium-calcium exchange may promote calcium entry into cardiac cells and trigger sarcoplasmic calcium release during physiologic action potentials.
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Normand Leblanc
University of Nevada, Reno
Joseph R. Hume
Electrophysiology
Science
University of Nevada, Reno
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Leblanc et al. (Fri,) conducted a other in Isolated cardiac myocytes. Membrane depolarization was evaluated on Release of calcium from cardiac sarcoplasmic reticulum. Sodium entry through tetrodotoxin-sensitive channels triggered calcium release from the sarcoplasmic reticulum via sodium-calcium exchange in isolated cardiac myocytes.
synapsesocial.com/papers/6a153a49cb0379474a8207aa — DOI: https://doi.org/10.1126/science.2158146