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. 2016 Mar 16;115(6):3174–3185. doi: 10.1152/jn.00036.2015

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Fig. 1. — Effect of the NO donors GSNO and SNAP on K_Na channel activity in isolated Kenyon cells. A, top: representative traces of K_Na channel current in the control (left) and 10 μM GSNO (right) groups. Bottom: corresponding all-point amplitude histograms. C and O, closed and complete opening levels, respectively. B: NP_o before the application of GSNO (Control), in the presence of 10 μM GSNO (GSNO), and after washout of GSNO (Wash-out). Matching symbols connected with a line show the sequential experiment in the same cell. C, top: representative traces of K_Na channel current in the control (left) and 10 μM SNAP (right) groups. Bottom: corresponding all-point amplitude histograms. D: NP_o before application of SNAP (Control), in the presence of 10 μM SNAP (SNAP), and after washout of SNAP (Wash-out). B and D: repeated-measures ANOVA.