vecuronium诱导的离体大鼠肌肉破伤风消退的机制。

M J de Oliveira, A C Oliveira
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引用次数: 10

摘要

结合肌图和电生理技术,在体外研究维库溴铵对强直收缩作用的细胞机制。我们采用离体大鼠坐骨神经指长伸肌制备。0.1 Hz脉冲诱发间接抽搐,50 Hz脉冲诱发破伤风。在50 Hz下产生端板电位序列。在分析终板电位时使用的电生理变量有:振幅、强直跳动、量子大小和量子含量。肌图研究表明,0.4 μ m维库溴铵引起强直性衰退,但不影响抽搐。在电生理方面,维库溴铵(0.4微米)降低了终板电位的振幅,增加了它们的强直损耗。这些变化是由于端板电位的量子含量和量子大小的显著减少。结论:维库溴铵在神经肌肉接点具有突触前和突触后作用,并通过这些作用的总和诱导强直收缩消退。
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Mechanisms underlying the vecuronium-induced tetanic fade in the isolated rat muscle.

The cellular mechanisms underlying the effects of vecuronium on the tetanic contraction were studied in vitro with a combination of myographic and electrophysiologic techniques. We used the isolated sciatic nerve extensor digitorum longus muscle preparation of the rat. Indirect twitches were evoked at 0.1 Hz pulses and tetani at 50 Hz pulses. Trains of end-plate potentials were generated at 50 Hz. The electrophysiological variables used in the analysis of the end-plate potentials were: amplitude, tetanic run-down, quantal size and quantal content. The myographic study demonstrated that vecuronium at 0.4 microM caused tetanic fade, but left the twitch unaffected. Regarding electrophysiology, vecuronium (0.4 microM) decreased the amplitude of end-plate potentials and increased their tetanic run-down. These changes were due to significant reductions in both the quantal content of the end-plate potentials and the quantal size. It is concluded that vecuronium has both pre- and postsynaptic effects at the neuromuscular junction, and that it induces fade of the tetanic contraction via a summation of these effects.

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