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. 1996 Oct 1;16(19):6125–6133. doi: 10.1523/JNEUROSCI.16-19-06125.1996

Fig. 1.

NMDAR overstimulation evokes persistent elevation of [Ca2+]i in hippocampal neurons. A, Time course of changes in [Ca2+]i of a neuron in response to K+-induced membrane depolarization (35 mm KCl, 30 sec, K+), followed by 20 min exposure to 200 μm NMDA. Values are plotted as relative pixel fluorescence intensity (F) normalized to baseline fluorescence values (F0); upward deflection denotes an increase in [Ca2+]i. Horizontal bars(gray background) indicate duration of treatment.Numbers indicate critical points in the Ca2+signal and code panels 1 to 7 that are pseudocolor digital images of Fluo-3 fluorescence (Kao et al., 1989).Pseudocolor scale represents arbitrary fluorescence intensity values ranging from 0 to 255. The KCl control stimulus elicits a rapid and reversible increase of [Ca2+]i (2). NMDA evokes a fast elevation of