A, somatic Ca2+ transients from 33 cells with decreasing and constant amplitudes were elicited by repetitive applications of GABA (G, 50 μm, 15 s pulse) and KCl (K20, 20 mm, 15 s pulse), respectively, in the presence of 0.3 μm TTX and 20 μm DNQX. Washout of TTX and DNQX (*) resulted in small spontaneous rises in [Ca2+]i in a few cells. After blockade of GABAA receptor-mediated inhibition (Bic, 20 μm), cells displayed spontaneous synchronized Ca2+ oscillations that were reversibly blocked by DNQX (20 μm). Synchronous activity ceased after washout of bicuculline. B, average of the 33 traces shown in A. Ca2+ transients were recorded in solutions buffered with HCO3−. Inset shows fluorescence image of Fura-2-AM-loaded neurons from this experiment excited at 357 nm; scale bar, 50 μm. The change in [Ca2+]i is presented as the change (Δ) in the fluorescence ratio obtained at the two excitation wavelengths (F357/F380). Δ is given in arbitrary units in this and all other figures.