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. 2010 Aug 11;30(32):10683–10691. doi: 10.1523/JNEUROSCI.5210-09.2010

Table 1.

Amperometric spike parameters from chromaffin cells in different experimental conditions

Imax (pA) Rise time (ms) Decay time (ms)
Control 83 ± 4 5.2 ± 0.3 7.7 ± 0.5
Anti-Syn (10 μm) 81 ± 7 5.9 ± 0.5 10.6 ± 0.8*
Anti-Dyn (10 μm) 78 ± 6 5.4 ± 0.4 10.3 ± 0.7*
Anti-His (10 μm) 77 ± 4 5.5 ± 0.4 8.1 ± 0.4
GST (40 μm) 88 ± 8 4.8 ± 0.3 7.3 ± 0.5
GST-Cterm (10 μm) 95 ± 4* 4.9 ± 0.4 8.6 ± 0.6
GST-Cterm + anti-Syn (10 μm) 89 ± 5 4.7 ± 0.2 7.2 ± 0.4
GST-Cterm (40 μm) 89 ± 4 4.8 ± 0.4 11.9 ± 0.6*
GST-Cterm + anti-Syn (40 μm) 90 ± 9 4.5 ± 0.5 7.1 ± 0.6
C-term240-290 (10 μm) 92 ± 4 5.7 ± 0.5 10.6 ± 1.0*
C-term240-290 + anti-Syn (10 μm) 85 ± 9 5.0 ± 0.3 7.1 ± 0.3

Control cells correspond to noninjected cells. Cells were injected with monoclonal anti-Syn, anti-Dyn, or anti-His antibodies. Cells were also injected with the following peptides: GST, GST-Cterm, and C-term240-290. Peptides encompassing the C terminal of synaptophysin were also coinjected with anti-Syn (GST-Cterm + anti-Syn; C-term240-290 + anti-Syn). Rise time, Time needed to reach Imax; Decay time, time constant of a single exponential fit to the decay phase. Data are means ± SEM of cell median for each spike parameters (12–24 cells from 3–5 different cultures).

*p < 0.05 compared with control cells.