Marek W, Ulmer W T
Professional Association's Research Institute of Occupational Medicine (BGFA) (Director; Prof. X. Baur, Ruhr University Bochum, Germany.
Respiration. 1995;62(6):322-30. doi: 10.1159/000196474.
The interaction of vagal neuronal and pharmacological mediator mechanisms on the airway-constrictory responses obtained from challenges with aerosolized methacholine (MCH) before and after bilateral vagotomy and in combination with electrical stimulation of the peripheral ends of the cut vagal nerves was investigated in anesthetized Ascaris allergen skin-sensitive sheep. Inhalation of aerosols of 2 and 5% MCH for 2 min in a control group of 10 sheep resulted in airway muscle constriction indicated by an increase in dynamic elastance (Edyn) (+70 and +256% of the basic value) or inspiratory airway resistance (RI) (+45 and +155%) and was associated with a significant rise in plasma histamine concentration (HiPl) from 0.2 +/- 0.2 to 0.9 +/- 1.1 and 1.5 +/- 1.2 ng/ml, respectively. Respiratory and cardiovascular responses to MCH were reproducible after 90 min of recovery. A second group of another 6 intact sheep showed similar alterations of respiratory mechanical parameters and HiPl after MCH challenges. After bilateral vagotomy, Edyn and RI increased after 2 and 5% MCH inhalation only by 15-30% of the control responses with intact vagi. The diminished airway constriction was associated with similar changes in HiP1 as observed with intact vagi. Inspite of severe cardiovascular responses, the most effective electrical stimulation of the peripheral ends of the vagal nerves resulted in an increase in Edyn or RI by only 40-50% of the basic value. In a tracheal segment beneath the cuff of the endotracheal tube isometric pressure effectively increased by almost 500% of the basic value. Vagus nerve stimulation was found without detectable changes in HiPl. Stimulation of the central ends of the vagal nerves did not induce airway constriction or alterations in HiPl. The combination of electrical vagus nerve stimulation and MCH inhalation resulted in a more than additive increase in Edyn and RI, but the airway responses did not reach the same level of obstruction after challenge with 5% MCH as observed with intact vagi. Electrical stimulation of the efferent vagi failed to stimulate spontaneous vagal nerve activity at higher levels of airway muscle responses. The results demonstrate that vagal neuronal mechanisms interact with local mediator liberation in acute airway obstruction. Airway challenge tests using cholinergic substances liberate histamine from inflammatory cells in the lungs of Ascaris skin-sensitive sheep.
在麻醉的蛔虫变应原皮肤敏感绵羊中,研究了迷走神经神经元和药理学介质机制对雾化乙酰甲胆碱(MCH)激发前后气道收缩反应的相互作用,以及与切断迷走神经外周端电刺激相结合的情况。在10只绵羊的对照组中,吸入2%和5%的MCH气雾剂2分钟,导致气道肌肉收缩,表现为动态弹性(Edyn)增加(分别为基础值的+70%和+256%)或吸气气道阻力(RI)增加(+45%和+155%),并与血浆组胺浓度(HiPl)从0.2±0.2显著升高至0.9±1.1和1.5±1.2 ng/ml相关。恢复90分钟后,对MCH的呼吸和心血管反应可重现。另一组6只完整绵羊在MCH激发后,呼吸力学参数和HiPl也有类似变化。双侧迷走神经切断后,吸入2%和5%的MCH后,Edyn和RI仅增加了完整迷走神经时对照反应的15 - 30%。气道收缩减弱与完整迷走神经时观察到的HiP1类似变化相关。尽管有严重的心血管反应,但对迷走神经外周端最有效的电刺激导致Edyn或RI仅增加基础值的40 - 50%。在气管插管袖口下方的气管段,等长压力有效增加了近基础值的500%。发现迷走神经刺激未引起HiPl可检测到的变化。刺激迷走神经中枢端未诱导气道收缩或HiPl改变。电刺激迷走神经与吸入MCH相结合导致Edyn和RI增加超过相加效应,但在5% MCH激发后,气道反应未达到完整迷走神经时观察到的相同阻塞水平。在较高水平的气道肌肉反应时,电刺激传出迷走神经未能刺激自发迷走神经活动。结果表明,在急性气道阻塞中,迷走神经神经元机制与局部介质释放相互作用。使用胆碱能物质进行气道激发试验可使蛔虫皮肤敏感绵羊肺部的炎性细胞释放组胺。