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. 2000 Jan 15;20(2):606–616. doi: 10.1523/JNEUROSCI.20-02-00606.2000

Fig. 7.

Fig. 7.

P2Y receptor activation inhibited ΔCm evoked by a train of depolarizing pulses. A, Superimposed Cmtraces recorded from a single cell in response to a train of twenty 20 msec depolarizing pulses to +20 mV from −90 mV. A control train (top trace) evoked an appreciable change inCm, and superfusion of 2-MeSATP (bottomtrace) inhibited the ΔCm in response to a subsequent train. Gaps in the traces and schematic in the top panelindicate timing of the pulses. B, Summary of the mean ± SEM inhibition of integrated Ca2+ entry (▿) and ΔCm (▴) by 2-MeSATP for each pulse in the train of depolarizations. Significant differences between inhibition of integrated Ca2+ entry and ΔCm changes are shown: ***p < 0.005; *p < 0.05 (n = 23). C, Plot of the mean Ca2+-dependence of ΔCmmeasured in response to a train of depolarizing pulses in the absence (♦) and presence (○) of 2-MeSATP (n = 23). Error bars are omitted for clarity.