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. 2017 Nov 15;7:15650. doi: 10.1038/s41598-017-15834-3

Table 1.

NaV channels in primary EC cells have similar properties.

ECJ ECC
Preps (n) 44 13
Cells (n) 125 18
P(INa) (%) 81.3 ± 4.0 64.1 ± 9.2
C (pF) 3.9 ± 1.0 2.1 ± 0.2*
IPEAK/C (pA/pF) −63.4 ± 5.6 −68.0 ± 11.5
GMAX (pA/pF) 1.57 ± 0.13 1.60 ± 0.19
V1/2I (mV) −48.2 ± 1.1 −53.3 ± 3.8
δVI 7.1 ± 0.1 8.9 ± 0.9
V1/2A (mV) −23.4 ± 0.9 −25.3 ± 2.2
δVA 6.7 ± 0.2 6.5 ± 0.3
EREV (mV) 39.0 ± 2.1 31.8 ± 4.3
τA (ms) 0.26 ± 0.02 0.23 ± 0.03
τF (ms) 1.00 ± 0.04 0.68 ± 0.04*
τS (ms) 11.4 ± 0.6 11.2 ± 1.1

Parameters of Na+ current under control conditions in CFP+ enterochromaffin cell cultures from mouse small bowel (ECJ) or colon (ECC). Preps, preparations of EC cell primary cultures. Cells, patch clamped murine TPH1-CFP+ EC cells with measurable Na+ current. P(I Na), average proportion of EC cells with measurable Na+ current in any given EC preparation. C, cell capacitance. I PEAK /C, peak Na+ current normalized to cell capacitance. G MAX, maximum conductance. V 1/2I, voltage of half inactivation. δV I, slope of voltage dependence of inactivation. V 1/2A, voltage of half activation. δV A, slope of voltage dependence of activation. E REV, reversal potential of Na+ current. τ A, time constant of activation. τ F, time constant of fast inactivation. τ S, time constant of slow inactivation. Values shown for time constants are at 0 mV. *P < 0.05 ECC vs. ECJ by a non-parametric two-tailed t-test.