Subcellular Ca²⁺ fluxes during ECC identified by fast Ca²⁺ imaging.

<p>A, global Ca²⁺ transient (ΔF/F₀) elicited by electrical field stimulation of a ventricular myocyte (panel <b>a</b>). Marker ‘1’ indicates the application of the electrical stimulus. Markers ‘2’ and ‘3’ were positioned according to the analysis in panel b. Panel <b>b</b>: first derivative of ΔF/F₀ (s⁻¹) from panel a, representing Ca²⁺ flux. Markers ‘2’ and ‘3’ indicate abrupt changes in Ca²⁺ flux rate, and marker ‘4’ indicates maximal Ca²⁺ flux. Panel <b>c</b>: spatially averaged Ca²⁺ flux under control conditions (Ctl) and during inhibition of SR function with thapsigargin (TG; 1 µM) and caffeine (Caff; 10 mM). <b>B</b>, subcellular Ca²⁺ transients (ΔF/F₀) elicited by electrical field stimulation and recorded from subsarcolemmal (SS) j-SR and central (CT) nj-SR regions of an atrial myocyte (panel <b>a</b>). Panel <b>b</b>: first derivative of SS and CT Ca²⁺ signals representing subcellular Ca²⁺ flux rates. Markers ‘1’ to ‘4’ as in panel A. Panel <b>c</b>: subcellular (SS, CT) Ca²⁺ flux rates in control and in the presence of thapsigargin+caffeine. 2-D images were recorded 1719 Hz time resolution.