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无阻断药物时哺乳动物标本中的神经肌肉传递及筒箭毒碱的作用。

Neuromuscular transmission in a mammalian preparation in the absence of blocking drugs and the effect of D-tubocurarine.

作者信息

Hubbard J I, Wilson D F

出版信息

J Physiol. 1973 Jan;228(2):307-25. doi: 10.1113/jphysiol.1973.sp010088.

Abstract
  1. Neuromuscular transmission in the presence and absence of D-tubocurarine was examined in cut muscle preparations of the rat diaphragm using intracellular recording techniques. The method of localizing the end-plates is described and evidence is presented indicating that end-plate potential (e.p.p.) recordings were made close to the end-plate region and that reliable estimates of the quantum content of e.p.p.s could be made.2. During repetitive nerve stimulation at rates between 2 and 10 Hz, e.p.p. amplitudes declined in response to the first 6-8 stimuli to reach a plateau level which was maintained for 1500 stimuli. At higher rates of stimulation some 500-700 stimuli were needed before a plateau level of amplitude was reached. It was demonstrated that these amplitude changes reflected similar changes in the quantal release of ACh.3. Tubocurarine in a concentration of 4 x 10(-8) g/ml. had no effect on quantal release but did reduce quantal size. In the presence of tubocurarine, 8 x 10(-8) g/ml., small reductions in the quantum content of the first e.p.p. in response to a train of stimuli and the maintained quantal release were observed. In the presence of tubocurarine 4 x 10(-7) g/ml., the quantum content of the first e.p.p. and the maintained release were further reduced, to the level previously described for curarized preparations. At this concentration a significant effect of tubocurarine upon the presynaptic measurements could be detected (t test). Studies on single junctions revealed that the post- and presynaptic effects of tubocurarine developed with different time courses.4. Neuromuscular preparations in vivo have been reported to be much more resistant to maintatined stimulation than curarized neuromuscular preparations in vitro. It is suggested that this disparity is explained by the presynaptic action of tubocurarine.5. From the quantal release rates of the present investigation and reports of ACh release/stimulus/end-plate in previous investigations it can be calculated that a quantum of ACh contains between 12,000 and 21,000 molecules.
摘要
  1. 运用细胞内记录技术,在大鼠膈肌的离体肌肉标本中,研究了有无筒箭毒碱(D - tubocurarine)存在时的神经肌肉传递。描述了定位终板的方法,并提供了证据表明终板电位(e.p.p.)记录是在靠近终板区域进行的,且能够对e.p.p.s的量子含量做出可靠估计。

  2. 在2至10赫兹的重复神经刺激期间,e.p.p.幅度在最初的6 - 8次刺激后下降,直至达到一个平台水平,并在随后的1500次刺激中保持稳定。在更高的刺激频率下,大约需要500 - 700次刺激才能达到幅度的平台水平。结果表明,这些幅度变化反映了乙酰胆碱(ACh)量子释放的类似变化。

  3. 浓度为4×10⁻⁸克/毫升的筒箭毒碱对量子释放没有影响,但会减小量子大小。在存在8×10⁻⁸克/毫升筒箭毒碱的情况下,观察到在一系列刺激下,第一个e.p.p.的量子含量有小幅下降,以及维持的量子释放也有下降。在存在4×10⁻⁷克/毫升筒箭毒碱的情况下,第一个e.p.p.的量子含量和维持释放进一步降低,达到了之前描述的箭毒化标本的水平。在此浓度下,可以检测到筒箭毒碱对突触前测量有显著影响(t检验)。对单个接头的研究表明,筒箭毒碱的突触后和突触前效应具有不同的时间进程。

  4. 据报道,体内的神经肌肉标本比体外箭毒化的神经肌肉标本对持续刺激的耐受性要强得多。有人认为,这种差异可以用筒箭毒碱的突触前作用来解释。

  5. 根据本研究的量子释放速率以及先前研究中ACh释放/刺激/终板的报告,可以计算出一个ACh量子包含12000至21000个分子。

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