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. 2011 Sep 8;106(6):1009–1022. doi: 10.1007/s00395-011-0218-4

Fig. 5.

Fig. 5

Characterisation of diastolic Ca2+ release events in the absence of ISO a perfusion protocol (upper) and typical records of Fuo-3 fluorescence (lower). b typical line scan images (upper) and corresponding fluorescence profiles (lower) in the presence of (i) 4.75 mmol/L [Ca2+]o and (ii) 4.75 mmol/L [Ca2+]o + 1.0 μmol/L K201; dashed lines (red) represent stimulus mark, circles represent wave initiation points. c mean ± SEM values of (i) number of wave initiation points/diastolic interval and (ii) fluorescence signals measured at the peak and at 950 ms post stimulation. White bars, 4.75: 4.75 mmol/L [Ca2+]o; Grey bars, 4.75 + K201: 4.75 mmol/L [Ca2+]o + 1.0 μmol/L K201; n = 4, *P < 0.05