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. 2019 Jun 5;127(6):067003. doi: 10.1289/EHP4583

Figure 7.

Figures 7A, 7B, and 7C show the gating kinetics of R y R1 channels influenced by nanomolar delt.methrin. Figure 7D shows three bar graphs plotting tau sub c with fold of control at 0.0, 0.5, 1.0, and 1.5; tau sub o with fold of control at 0.0, 1.0, 2.0, and 3.0; and P sub o with fold of control at 0.0, 20.0, 40.0, and 60.0 (y-axis) across deltamethrin at three independent channels of control, 10, and 30 nanomolars (x-axis), representing data as standard error of mean.

Influence of nanomolar DM on the gating kinetics of RyR1 channels. (A–C) Representative traces of RyR1 activity in single-channel level in the (A) absence, and (B) presence of 10  nM and (C) 30  nM, respectively. (D) Analysis of the gating parameters of mean closed time (τc) (top), mean open time (τo) (middle), and open probability (Po) (bottom). Each data point represents the mean±standard error of the mean  (SEM) from three independent channels. Statistical significance between groups was calculated by one-way analysis of variance (ANOVA) followed by post hoc Bonferroni comparison. Note: C, closed state of the channel; DM, deltamethrin; O, open state of the RyR1 channel; Po, open probability; RyRs, ryanodine receptors; τo, mean open time; τc, mean closed time. **p<0.01, DM vs. control.