Fig. 6.
Influence of the severity of myasthenia gravis (MG) on endplate potential (EPP). Amplitude of the first EPP (EPP1amp; A) and the quotient between the averaged amplitude from the 21st to the 50th EPPs (EPP21–50amp) and EPP1amp, as an indication of EPP run-down (B), were significantly smaller at 0% inhibitory concentration (IC0) for first evoked isometric twitch tension of rocuronium in the moderate and severe MG groups than in the sham group. Quantal content of EPP1 (QC1; C) and EPP21–50 (QC21–50; D) were significantly different at IC0 of rocuronium among the three groups. EPP1amp (A) was significantly decreased by administration of IC50 of rocuronium in the three groups (A), whereas indicators of EPP run-down (B), QC1 (C), and QC21–50 (D) were significantly decreased in the sham and moderate MG groups by administration of IC50 of rocuronium. Data are shown as means ± SD, n = 8 in each group. **P < 0.01 versus sham group at IC0 of rocuronium, ††P < 0.01 versus moderate MG group at IC0 of rocuronium, §§P < 0.01 versus each group at IC0 of rocuronium. Data were analyzed by using two-way repeated-measures ANOVA with the Tukey test among three groups and two-tailed paired t test with Bonferroni correction between IC0 and IC50 in each group.

Influence of the severity of myasthenia gravis (MG) on endplate potential (EPP). Amplitude of the first EPP (EPP1amp; A) and the quotient between the averaged amplitude from the 21st to the 50th EPPs (EPP21–50amp) and EPP1amp, as an indication of EPP run-down (B), were significantly smaller at 0% inhibitory concentration (IC0) for first evoked isometric twitch tension of rocuronium in the moderate and severe MG groups than in the sham group. Quantal content of EPP1 (QC1; C) and EPP21–50 (QC21–50; D) were significantly different at IC0 of rocuronium among the three groups. EPP1amp (A) was significantly decreased by administration of IC50 of rocuronium in the three groups (A), whereas indicators of EPP run-down (B), QC1 (C), and QC21–50 (D) were significantly decreased in the sham and moderate MG groups by administration of IC50 of rocuronium. Data are shown as means ± SD, n = 8 in each group. **P < 0.01 versus sham group at IC0 of rocuronium, ††P < 0.01 versus moderate MG group at IC0 of rocuronium, §§P < 0.01 versus each group at IC0 of rocuronium. Data were analyzed by using two-way repeated-measures ANOVA with the Tukey test among three groups and two-tailed paired t test with Bonferroni correction between IC0 and IC50 in each group.

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