Wessler I, Klein A, Pohan D, Maclagan J, Racké K
Department of Pharmacology, University of Mainz, Federal Republic of Germany.
Naunyn Schmiedebergs Arch Pharmacol. 1991 Oct;344(4):403-11. doi: 10.1007/BF00172579.
Basal and stimulated outflow of radioactive acetylcholine, phosphorylcholine and choline from rat and guinea-pig isolated tracheae were measured by reverse phase HPLC followed by liquid-scintillation-spectrometry. Tracheae were stimulated either by an electrical field (transmural stimulation) or by a local stimulation of the innervating parasympathetic nerves (preganglionic stimulation). Epithelium was removed in most experiments, as the epithelium inhibits acetylcholine release. The basal tritium efflux (1,600 dpm/3 min) from rat isolated tracheae incubated with [3H]choline consisted of 56% [3H]phosphorylcholine and 38% [3H]choline. Preganglionic stimulation (15 Hz, 1,200 pulses) caused a 2-fold increase in tritium outflow that was abolished by the removal of extracellular calcium or by the addition of tetrodotoxin. The stimulated outflow of tritium induced by preganglionic nerve stimulation was caused by an exclusive release of [3H]acetylcholine, whereas the efflux of [3H]phosphorylcholine and [3H]choline remained unaffected by this stimulation mode. Transmural stimulation of the rat or guinea-pig trachea, however, caused, in addition to the release of [3H]acetylcholine, the outflow of [3H]phosphorylcholine. Hexamethonium (300 mumol/l) or tubocurarine (100 mumol/l) inhibited (80%) the increase in tritium outflow evoked by preganglionic stimulation, but did not affect tritium outflow evoked by transmural stimulation. Oxotremorine reduced [3H]acetylcholine release evoked by both stimulation modes, but oxotremorine was less potent with transmural stimulation. Scopolamine (0.3 mumol/l) enhanced (120%) the release of [3H]acetylcholine evoked by preganglionic nerve stimulation indicating the blockade of an endogenous negative muscarinic feedback mechanism. Epithelium-dependent inhibition of [3H]acetylcholine release was evident with both preganglionic and transmural stimulation. The present experiments demonstrate that release of [3H]acetylcholine evoked from the isolated trachea by stimulation of the preganglionic trunk of the parasympathetic cholinergic nerves.(ABSTRACT TRUNCATED AT 250 WORDS)
通过反相高效液相色谱法结合液体闪烁光谱法,测量了大鼠和豚鼠离体气管中放射性乙酰胆碱、磷酰胆碱和胆碱的基础分泌量及刺激后的分泌量。气管通过电场(跨壁刺激)或支配的副交感神经局部刺激(节前刺激)进行刺激。在大多数实验中去除了上皮,因为上皮会抑制乙酰胆碱释放。用[³H]胆碱孵育的大鼠离体气管的基础氚流出量(1600 dpm/3分钟)中,56%为[³H]磷酰胆碱,38%为[³H]胆碱。节前刺激(15 Hz,1200个脉冲)使氚流出量增加了两倍,去除细胞外钙或添加河豚毒素可消除这种增加。节前神经刺激诱导的氚刺激流出是由[³H]乙酰胆碱的单独释放引起的,而[³H]磷酰胆碱和[³H]胆碱的流出不受这种刺激模式的影响。然而,大鼠或豚鼠气管的跨壁刺激,除了[³H]乙酰胆碱的释放外,还导致[³H]磷酰胆碱的流出。六甲铵(300 μmol/L)或筒箭毒碱(100 μmol/L)抑制(80%)节前刺激引起的氚流出增加,但不影响跨壁刺激引起的氚流出。氧化震颤素减少了两种刺激模式引起的[³H]乙酰胆碱释放,但氧化震颤素对跨壁刺激的作用较弱。东莨菪碱(0.3 μmol/L)增强(120%)节前神经刺激引起的[³H]乙酰胆碱释放,表明内源性负毒蕈碱反馈机制被阻断。上皮依赖性对[³H]乙酰胆碱释放的抑制在节前和跨壁刺激中均很明显。本实验表明,刺激副交感胆碱能神经的节前干可从离体气管中诱发[³H]乙酰胆碱的释放。(摘要截于250字)