Fig. 4.
Effects of 400 µM isoflurane on the activity of inositol trisphosphate receptor (InsP3R) channel in various [InsP3]. (A–D) Typical single-channel current traces of InsP3R channels in various [InsP3] in the absence and presence of 400 μM isoflurane, as indicated. Currents shown were recorded at room temperature with applied potential (Vapp) = −40 mV, and arrows indicate the closed channel current level. See figure 1, A–C, for InsP3R channel current traces in 0, 1, and 10 μM InsP3 with no isoflurane, and figure 1D for InsP3R channel current trace in 400 μM isoflurane only. (E) Statistically similar InsP3R channel activities (P > 0.05, ANOVA test) were observed in 100 nM ≤ [InsP3] ≤ 1 μM in the absence of isoflurane. With 400 μM isoflurane, statistically similar InsP3R channel activities (P > 0.05, ANOVA test) were also observed in 0 ≤ [InsP3] ≤ 1 μM. Importantly, 400 μM isoflurane significantly increased InsP3R channel activity at low [InsP3] (0, 100, and 500 nM). Error bars indicate SEM, and number of experiments analyzed is tabulated. **, *P (t test) <0.005 and 0.05, respectively, for the quantities connected by the brackets. InsP3R channel Po in saturating 10 μM InsP3 were significantly higher (P < 0.05, t test with Bonferronic correction) than those in subsaturating [InsP3], in the presence or absence of 400 μM isoflurane. However, InsP3R channel activity in saturating (10 μM) InsP3 was not enhanced by 400 μM isoflurane (P > 0.05, t test).

Effects of 400 µM isoflurane on the activity of inositol trisphosphate receptor (InsP3R) channel in various [InsP3]. (AD) Typical single-channel current traces of InsP3R channels in various [InsP3] in the absence and presence of 400 μM isoflurane, as indicated. Currents shown were recorded at room temperature with applied potential (Vapp) = −40 mV, and arrows indicate the closed channel current level. See figure 1, A–C, for InsP3R channel current traces in 0, 1, and 10 μM InsP3 with no isoflurane, and figure 1D for InsP3R channel current trace in 400 μM isoflurane only. (E) Statistically similar InsP3R channel activities (P > 0.05, ANOVA test) were observed in 100 nM ≤ [InsP3] ≤ 1 μM in the absence of isoflurane. With 400 μM isoflurane, statistically similar InsP3R channel activities (P > 0.05, ANOVA test) were also observed in 0 ≤ [InsP3] ≤ 1 μM. Importantly, 400 μM isoflurane significantly increased InsP3R channel activity at low [InsP3] (0, 100, and 500 nM). Error bars indicate SEM, and number of experiments analyzed is tabulated. **, *P (t test) <0.005 and 0.05, respectively, for the quantities connected by the brackets. InsP3R channel Po in saturating 10 μM InsP3 were significantly higher (P < 0.05, t test with Bonferronic correction) than those in subsaturating [InsP3], in the presence or absence of 400 μM isoflurane. However, InsP3R channel activity in saturating (10 μM) InsP3 was not enhanced by 400 μM isoflurane (P > 0.05, t test).

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