Circulation Research · 2002 · 191 citations · 30 references
Natural SciencesBiophysicsPhysiologyCell SignalingElectrophysiologyIon Channel BiophysicsAction PotentialsCardiac Action PotentialsCardiac PhysiologyIon ChannelsMembrane ElectrophysiologyVentricular ElectrophysiologyCardiac Action Potential PhysiologyCardiac Ion Channel RegulationCardiac RepolarizationCurrent-voltage RelationshipIntracellular Ventricular ElectrophysiologySteady-state VoltageVentricular Action PotentialsVoltage-dependence Of Channel Activation
Na(+)-Ca(2+) exchange (NCX) is crucial in the regulation of [Ca(2+)](i) and cardiac contractility, but key details of its dynamic function during the heartbeat are not known. In the present study, we assess how NCX current (I(NCX)) varies during a rabbit ventricular action potential (AP). First, we measured the steady-state voltage and [Ca(2+)](i) dependence of I(NCX) under conditions when [Ca(2+)](i) was heavily buffered. We then used this relationship to infer the submembrane [Ca(2+)](i) ([Ca(2+)](sm)) sensed by NCX during a normal AP and [Ca(2+)](i) transient (when the AP was interrupted to produce an I(NCX) tail current). The [Ca(2+)](i) dependence of I(NCX) at -90 mV allowed us to convert the peak inward I(NCX) tail currents to [Ca(2+)](sm). Peak [Ca(2+)](sm) measured via this technique was >3.2 micromol/L within < 32 ms of the AP upstroke (versus peak [Ca(2+)](i) of 1.1 micromol/L at 81 ms measured with the global Ca(2+) indicator indo-1). The voltage and [Ca(2+)](sm) dependence of I(NCX) allowed us to infer I(NCX) during the normal AP and Ca(2+) transient. The early rise in [Ca(2+)](sm) causes I(NCX) to be inward for the majority of the AP. Thus, little Ca(2+) influx via NCX is expected under physiological conditions, but this can differ among species and in pathophysiological conditions.
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Arrhythmogenesis and Contractile Dysfunction in Heart Failure
Steven M. Pogwizd, Klaus Schlotthauer, Li Li et al. · Circulation Research · 2001 · 757 citations · Full text
Medicine, Cardiology, Physiology +17
Gene expression of the cardiac Na(+)-Ca2+ exchanger in end-stage human heart failure.
R. Studer, Hans Reinecke, Johannes Bilger et al. · Circulation Research · 1994 · 632 citations