Bukharaeva E A, Kim K K, Nikol'skii E E, Vyskochil F
Kazan' State Medical University, Russia.
Neurosci Behav Physiol. 2000 Mar-Apr;30(2):139-46. doi: 10.1007/BF02463151.
Experiments on frog neuromuscular junction preparations with extracellular recording of nerve terminal action potentials and single-quantum end-plate currents (EPC) were used to assess the time course of evoked quantum secretion of mediator by analyzing histograms of the distribution of true synaptic delays. These studies showed that noradrenaline, isoproterenol, and dobutamine change the kinetics of secretion of quanta, leading to synchronization of the process of mediator release; substances blocking beta-adrenoceptors (atenolol, propranolol) blocked this effect. Clonidine and phenylephrine, which activate alpha-receptors, had no effect on the kinetics of secretion, while the alpha-blocker phentolamine had no effect on the synchronizing action of noradrenaline. Reconstruction of multiquantum EPC from changes in the level of synchronization in the release of individual quanta, showed that EPC amplitude increased in response to noradrenaline by 17%, and that this was due only to alterations in the time course of secretion. These data led to the conclusion that there is a special presynaptic mechanism which facilitates the action of sympathomimetics, acting via beta-adrenoceptors.
通过细胞外记录神经末梢动作电位和单量子终板电流(EPC),对青蛙神经肌肉接头标本进行实验,以通过分析真实突触延迟分布的直方图来评估诱发的介质量子分泌的时间进程。这些研究表明,去甲肾上腺素、异丙肾上腺素和多巴酚丁胺改变了量子分泌的动力学,导致介质释放过程同步;阻断β-肾上腺素能受体的物质(阿替洛尔、普萘洛尔)阻断了这种效应。激活α-受体的可乐定和去氧肾上腺素对分泌动力学没有影响,而α-阻滞剂酚妥拉明对去甲肾上腺素的同步作用也没有影响。根据单个量子释放同步水平的变化重建多量子EPC,结果表明,去甲肾上腺素使EPC幅度增加了17%,这仅归因于分泌时间进程的改变。这些数据得出结论,存在一种特殊的突触前机制,该机制促进了通过β-肾上腺素能受体起作用的拟交感神经药的作用。