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. 1998 May 15;509(Pt 1):103–116. doi: 10.1111/j.1469-7793.1998.103bo.x

Table 1.

Comparison of [Ca2+]i and [Na+]i at 2 min following washout in Ca2+-free, Na+-free, or Ca2+- and Na+-free buffers

Condition [Ca2+]1 (%) [Na+]1 (%)
Control 33.6 ± 4.7 73.7 ± 4.9
Ca2+ free 23.5 ± 4.0 80.0 ± 2.6
Na+ free 63.2 ± 4.8 * 47.4 ± 4.5 *
Ca2+, Na+ free 24.6 ± 3.4 55.3 ± 3.7 *

Neurones were stimulated with kainate (100 μm) for 15 s. Values shown are the respective intracellular ion concentration measured 2 min after agonist washout as a percentage of the peak value determined in the presence of agonist. The fluo-3 signal was measured as background-subtracted fluorescence intensity, while the SBFI data have been converted from ratios into [Na+]i as described in Methods. These data represent means ±s.e.m. of 5 different coverslips, with 10-36 cells for each coverslip.

*

Significantly different from control (P < 0.05, ANOVA with Dunnett's correction for multiple comparisons).