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. 2010 Mar 19;298(6):H1939–H1950. doi: 10.1152/ajpheart.00607.2009

Fig. 2.

Fig. 2.

ATP-induced increases in intracellular Ca2+ concentration ([Ca2+]i) in Ca2+-buffered developing cardiomyocytes. A: normalized fluorescence images from a neonatal cardiomyocyte show low noise before activation (control; F/Fo ≅ 1) and subsarcolemmal increases in [Ca2+]i following application of 100 μM ATP. B: average cellular Ca2+ transients (ΔF/Fo) in neonatal (Neo; solid bars; 1 to 2 days old) and juvenile (Juv; hatched bars; 8–10 days old) cardiomyocytes in response to 100 μM ATP (left) or 100 nM endothelin-1 (ET-1; right). Voltage-clamped cells are same color scale as Fig. 1.