Habermeier-Muth A, Muscholl E
Pharmakologisches Institut, Universität Mainz, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 1995 Feb;351(2):156-63. doi: 10.1007/BF00169329.
The aim of the present study was to explore possible prejunctional effects mediated by impulse activity of sympathetic terminals on evoked acetylcholine release in an organ innervated by the autonomic ground plexus. Rabbit atria were isolated with the extrinsic right vagus and sympathetic nerves intact and perfused with Tyrode solution. Acetylcholine overflow was determined after labelling of the transmitter stores with [14C]choline and fractionation of the radioactivity on cation exchange columns. The overflow of endogenous noradrenaline was measured by HPLC and electrochemical detection. The vagus nerve was stimulated at 2 Hz for 3 min four times at intervals of 10 min. During the second stimulation the postganglionic sympathetic nerves were stimulated (2 Hz, 3 min) in such a way that the impulses preceded the vagus stimuli by a fixed time interval which was varied in different experiments (0, 7, 19, 50, 132, and 350 ms). Evoked acetylcholine release was significantly enhanced when the vagus was excited 7, 19 and 50 ms after the sympathetic nerves but it was unaltered at the 132 or 350 ms intervals, and when both nerves were stimulated simultaneously. Noradrenaline release was similar (about 6 ng per stimulation period) in all experimental groups. When sympathetic nerve stimulation had little effect in releasing noradrenaline (< 2.0 ng per stimulation period), facilitation of acetylcholine release at the 19 ms pulse interval was absent. The resting outflow of acetylcholine was unaffected by sympathetic nerve stimulation. The experiments show a facilitation of evoked acetylcholine release by sympathetic activity. As revealed by the pulse-to-pulse method this effect is confined to a relatively brief interval immediately following the excitation of the noradrenergic terminal, and is unlikely to be mimicked by exogenous drug application.
本研究的目的是探讨自主神经丛支配的器官中,交感神经末梢冲动活动介导的对诱发乙酰胆碱释放的可能的接头前效应。分离出兔心房,保留其右侧迷走神经和交感神经的完整性,并用台氏液灌注。在用[14C]胆碱标记递质储存并在阳离子交换柱上分离放射性后,测定乙酰胆碱的溢出量。用高效液相色谱法和电化学检测法测量内源性去甲肾上腺素的溢出量。以2 Hz的频率刺激迷走神经,每次刺激3分钟,间隔10分钟,共刺激4次。在第二次刺激期间,以这样的方式刺激节后交感神经(2 Hz,3分钟),即冲动比迷走神经刺激提前一个固定的时间间隔,该时间间隔在不同实验中有所变化(0、7、19、50、132和350毫秒)。当交感神经兴奋后7、19和50毫秒刺激迷走神经时,诱发的乙酰胆碱释放显著增强,但在132或350毫秒的间隔以及同时刺激两条神经时,乙酰胆碱释放没有变化。所有实验组中去甲肾上腺素的释放量相似(每次刺激期约6纳克)。当交感神经刺激在释放去甲肾上腺素方面作用很小时(每次刺激期<2.0纳克),在19毫秒的脉冲间隔时乙酰胆碱释放的促进作用不存在。乙酰胆碱的静息流出不受交感神经刺激的影响。实验表明交感神经活动促进了诱发的乙酰胆碱释放。通过逐脉冲法揭示,这种效应局限于去甲肾上腺素能末梢兴奋后紧接着的一个相对较短的时间间隔内,并且不太可能被外源性药物应用所模拟。