Fig. 3. Comparative antagonism of gantacurium (0.5 mg/kg or ∼5 × ED95) by edrophonium (1.0 mg/kg with atropine 0.05 mg/kg) or l-cysteine (10 mg/kg). Gantacurium was injected at t = 0. Antagonist was given at the beginning of recovery at 2% twitch height (standard antagonism, B ); or at 1 min after gantacurium administration (immediate antagonism, A ). Antagonism by l-cysteine is faster than edrophonium at 2% twitch and is equally rapid at either 2% twitch or at 1 min after gantacurium (P < 0.05). Antagonism by l-cysteine at 1 min is significantly faster (P < 0.001) than edrophonium, which shifts the dose–duration curve to the left by only ∼2 min. Curves show summarized data from experiments in anesthetized rhesus monkeys in which twitch of the extensor digitorum was elicited at 0.15 Hz (see also fig. 4).

Fig. 3. Comparative antagonism of gantacurium (0.5 mg/kg or ∼5 × ED95) by edrophonium (1.0 mg/kg with atropine 0.05 mg/kg) or l-cysteine (10 mg/kg). Gantacurium was injected at t = 0. Antagonist was given at the beginning of recovery at 2% twitch height (standard antagonism, B ); or at 1 min after gantacurium administration (immediate antagonism, A ). Antagonism by l-cysteine is faster than edrophonium at 2% twitch and is equally rapid at either 2% twitch or at 1 min after gantacurium (P < 0.05). Antagonism by l-cysteine at 1 min is significantly faster (P < 0.001) than edrophonium, which shifts the dose–duration curve to the left by only ∼2 min. Curves show summarized data from experiments in anesthetized rhesus monkeys in which twitch of the extensor digitorum was elicited at 0.15 Hz (see also fig. 4).

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