Hirshman C A, Downes H
J Appl Physiol Respir Environ Exerc Physiol. 1981 Apr;50(4):761-5. doi: 10.1152/jappl.1981.50.4.761.
To test the relative importance of cholinergic effects on the Basenji-Greyhound (BG) model of asthma, we administered Ascaris antigen to Ascaris-sensitive BG dogs without other treatment, and following intravenous atropine. Pulmonary resistance (RL) increased from 1.4 +/- 0.43 cmH2O . l-1 . s (mean + SE) to 26.0 +/- 5.21 after Ascaris antigen exposure in seven untreated dogs. In the same dogs pretreated with 0.2 mg/kg atropine, RL increased from 1.5 +/- 0.31 to 18 +/- 5.00. Atropine 0.4 and 1.0 mg/kg did not result in increased protection. Although 0.2 mg/kg atropine markedly inhibited the airway responses to both inhaled citric acid and methacholine, it only slightly prevented antigen-induced airway constriction. We conclude that in BG dogs, cholinergic pathways elicit bronchomotor responses to irritants but that the major component of antigen-induced bronchoconstriction is not cholinergically mediated.
为了测试胆碱能效应在哮喘巴仙吉犬-灵缇犬(BG)模型中的相对重要性,我们在未进行其他处理以及静脉注射阿托品后,给对蛔虫敏感的BG犬注射蛔虫抗原。7只未处理的犬在接触蛔虫抗原后,肺阻力(RL)从1.4±0.43厘米水柱·升⁻¹·秒(均值±标准误)增加到26.0±5.21。在用0.2毫克/千克阿托品预处理的同一只犬中,RL从1.5±0.31增加到18±5.00。0.4毫克/千克和1.0毫克/千克的阿托品并未带来更大的保护作用。尽管0.2毫克/千克阿托品显著抑制了气道对吸入柠檬酸和乙酰甲胆碱的反应,但它仅略微预防了抗原诱导的气道收缩。我们得出结论,在BG犬中,胆碱能途径引发对刺激物的支气管运动反应,但抗原诱导的支气管收缩的主要成分并非由胆碱能介导。