首页> 外文期刊>The Journal of Physiology >Long-term in vivo modulation of synaptic efficacy at the neuromuscular junction of Rana pipiens frogs.
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Long-term in vivo modulation of synaptic efficacy at the neuromuscular junction of Rana pipiens frogs.

机译:长期在体内调节突触蛙的神经肌肉交界处的突触效力。

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摘要

Prolonged changes in motor neurone activity can result in long-term changes in synaptic transmission. We investigated whether mechanisms commonly thought to be involved in determining synaptic efficacy of vertebrate motor neurones are involved in these long-term changes. The nerve supplying the cutaneous pectoris muscle was chronically stimulated via skin surface electrodes in freely moving frogs for 5-7 days. Chronic stimulation induced a 50% reduction in evoked endplate potential (EPP) amplitude at stimulated neuromuscular junctions (NMJs). These changes appear to be presynaptic since miniature EPP (mEPP) amplitude was unchanged while mEPP frequency was decreased by 46% and paired-pulse facilitation was increased by 26%. High frequency facilitation (40 Hz, 2 s) was also increased by 89%. Moreover, stimulated NMJs presented a 92% decrease in synaptic depression (40 Hz, 2 s). An increase in mitochondrial metabolism was observed as indicated by a more pronounced labelling of active mitochondria (Mitotracker) in stimulated nerve terminals, which could account for their greater resistance to synaptic depression. NMJ length visualized by alpha-bungarotoxin staining of nAChRs was not affected. Presynaptic calcium signals measured with Calcium Green-1 were larger in stimulated NMJs at low frequency (0.2 Hz) and not different from control NMJs at higher frequency (40 Hz, 2 s and 30 s). These results suggest that some mechanisms downstream of calcium entry are responsible for the determination of synaptic output, such as a down-regulation of some calcium-binding proteins, which could explain the observed results. The possibility of a change in frequenin expression, a calcium-binding protein that is more prominently expressed in phasic synapses, was, however, refuted by our results.
机译:运动神经元活性的长期变化可导致突触传递的长期变化。我们调查了通常认为与确定脊椎动物运动神经元的突触功效有关的机制是否与这些长期变化有关。通过皮肤表面电极在自由移动的青蛙中长期刺激供应皮肤胸肌的神经5-7天。慢性刺激引起神经肌肉接头(NMJs)诱发的终板电位(EPP)幅度降低50%。这些变化似乎是突触前的,因为微型EPP(mEPP)幅度没有变化,而mEPP频率降低了46%,而配对脉冲易化性提高了26%。高频简化(40 Hz,2 s)也增加了89%。此外,受刺激的NMJs突触抑制能力降低了92%(40 Hz,2 s)。刺激的神经末梢中活性线粒体(Mitotracker)的标记更为明显,表明线粒体代谢增加,这可能说明它们对突触抑制的抵抗力增强。通过nAChRs的α-真菌毒素染色可见的NMJ长度不受影响。用钙绿1测定的突触前钙信号在低频(0.2 Hz)下受刺激的NMJ较大,而与较高频率(40 Hz,2 s和30 s)的对照NMJ相同。这些结果表明,钙进入下游的某些机制负责确定突触输出,例如一些钙结合蛋白的下调,这可以解释观察到的结果。然而,我们的研究结果驳斥了弗雷明宁表达发生改变的可能性,弗雷明宁表达是一种在阶段性突触中更明显表达的钙结合蛋白。

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