A, top: AP-clamp experiment showing representative ctrl spike. (middle) Kv currents (red traces) were measured in a Tyrode standard solution with TTX (300 nm) and Cd2+ (200 μm). Ca2+ currents (black) were measured in the presence of TTX (300 nm) and high extracellular TEA (135 mm). Ca2+-activated K+ currents (blue) were obtained by subtracting from a control recording in Tyrode standard with TTX (300 nm) the KV and the Ca2+ current. Bottom: close up. The grey rectangle indicates the AHP phase and the respective currents that sustain it. B and C, as for A, using a single spike stimulus protocol triggered from −40 mV and a spike doublet fired after complete block of Nav currents with 300 nm TTX. B, inset: net current amplitudes measured during the AHP phase indicated by the grey windows. C, inset: Ca2+ charge entering the cell during the AHP phase calculated by the integrating the corresponding Ca2+ inward current (*P < 0.05; ***P < 0.001; n = 9; ANOVA followed by a post hoc Bonferroni analysis).