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

机译:在不存在封闭药物的情况下哺乳动物制剂中的神经肌肉传递和D-微管尿素的作用

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摘要

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 × 10-8 g/ml. had no effect on quantal release but did reduce quantal size. In the presence of tubocurarine, 8 × 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 × 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.
机译:1.使用细胞内记录技术在大鼠diaphragm肌的切开的肌肉制剂中检查存在和不存在D-微管尿素时的神经肌肉传递。描述了端板的定位方法,并提供了证据表明端板电位(e.p.p.)记录靠近端板区域,并且可以对e.p.p.s的量子含量进行可靠的估算。2。在重复性神经刺激期间,频率为2到10 Hz。振幅响应于最初的6-8刺激而下降,直至达到1500刺激的平稳水平。在较高的刺激速率下,在达到平稳水平的振幅之前,需要约500-700个刺激。结果表明,这些幅度变化反映了ACh.3定量释放中的类似变化。图布库拉林的浓度为4×10 -8 g / ml。对定量释放没有影响,但确实减小了定量大小。在存在8×10 -8 g / ml的微管尿素时,第一个e.p.p.响应一系列刺激,观察到维持的定量释放。在微管尿素4×10 -7 g / ml的存在下,第一个e.p.p.缓释剂和缓释剂的含量进一步降低至先前对固化制剂所述的水平。在该浓度下,可以检测到微管尿素对突触前测量的显着影响(t检验)。对单个连接点的研究表明,微管尿素的突触后和突触前效应随着时间的推移而发展。4。据报道,体内的神经肌肉制剂比体外整理的神经肌肉制剂对维持刺激的抵抗力强得多。建议这种差异可以通过微管神经素的突触前作用来解释。5。根据当前研究的定量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ACh的量子包含12,000到21,000个分子。

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