Patterson R, Harris K E
J Lab Clin Med. 1976 Jan;87(1):65-72.
Rhesus monkeys with reagin-mediated, immediate-type respiratory responses to ascaris antigen were used for comparison with the type of responses that occur from certain pharmacologic agents. Carbacholine produces a respiratory response that is the same type as an antigen-induced respiratory response and will sensitize an animal's airway so that a dose of antigen not reactive alone will stimulate a response. Antigen and histamine will sensitize the airway so that a subthreshold dose of carbacholine will produce a respiratory response. Atropine completely inhibited the carbacholine response and reversed the increased sensitivity to carbacholine that occurs after an antigen response. Atropine did not block the antigen-induced respiratory response or the respiratory response to prostagladin F2alpha. Partial inhibition of these responses may have occurred but was not detected in the systems used in these studies. A double-antigen challenge system in the rhesus model of asthma provides a useful technique for evaluating the effect of pharmacologic agents on the reagin-mediated respiratory response.
对蛔虫抗原有反应素介导的速发型呼吸反应的恒河猴被用于与某些药物制剂所引发的反应类型进行比较。卡巴胆碱产生的呼吸反应与抗原诱导的呼吸反应类型相同,并且会使动物气道致敏,从而使单独无反应的一定剂量抗原能够刺激产生反应。抗原和组胺会使气道致敏,以至于低于阈值剂量的卡巴胆碱会产生呼吸反应。阿托品完全抑制了卡巴胆碱反应,并逆转了抗原反应后出现的对卡巴胆碱敏感性增加的情况。阿托品并未阻断抗原诱导的呼吸反应或对前列腺素F2α的呼吸反应。这些反应可能发生了部分抑制,但在这些研究中所使用的系统中未检测到。恒河猴哮喘模型中的双抗原激发系统为评估药物制剂对反应素介导的呼吸反应的影响提供了一种有用的技术。