A, a myocyte was first dialysed with cA-PK inhibitory peptide (PKI; 20 μm) and exposed to external control solution. Applications of Iso (100 pM, 10 nm) and SNAP (1 nm, 1 μm) are indicated by the lines. Traces were recorded at the times indicated by the corresponding letters on the main graph (a-h). The dotted line indicates the zero-current level. B, summary of the effects of Iso (100 pm), SNAP (1 nm, 1 μm), in myocytes dialysed with PKI (20 μm). C, overview of the effects of Iso (1–100 pm), SNAP (1 nm), in the absence or in the presence of external adenosine-3′,5′-cyclic monophosphothioate, Rp-isomer (Rp-cA 300 μm). The amplitude of ICa,L in the presence of agonists was normalised to the amplitude of the basal ICa,L in the absence of agonists. Bars are the means and vertical lines are the s.e.m. of the number of experiments indicated near the bars. Significant differences from the Iso (*) or the Iso plus SNAP (#) levels: *P≤ 0.05; #P≤ 0.01.