Misawa M, Chiba Y
Department of Pharmacology, School of Pharmacy, Hoshi University, Tokyo, Japan.
Jpn J Pharmacol. 1993 Jan;61(1):41-50. doi: 10.1254/jjp.61.41.
Airway hyperresponsiveness (AHR) is a critical component in bronchial asthma, but the underlying mechanisms remain to be disclosed. Our present studies were performed to establish a new good experimental animal model of AHR. Male Wistar rats actively sensitized with DNP-Ascaris antigen (DNP-Asc) were challenged by inhaling DNP-Asc 8 days after the first immunization (single antigenic challenge). Another sensitization group received 3 challenges every 48 hr (repeated antigenic challenge). The airway responsiveness to inhalations of acetylcholine (ACh) and neurokinin A (NKA) were determined under anesthesia. The airway microvascular leakage was also determined with Evans blue (E.B.). At 24 hr after the single antigen challenge, the airway responsiveness to ACh and NKA were slightly enhanced, and the E.B. exudation was increased in the main bronchus. In contrast, the airway responsiveness to ACh and NKA and the E.B. exudation in the main bronchus were much more markedly enhanced 24 hr after the repeated antigenic challenge. The isolated main bronchial strip from the challenged rats had obtained AHR towards ACh and serotonin. These findings suggest that repeated antigenic challenge causes a distinct AHR, both in vivo and in vitro, and that the airway inflammation may be closely related to pathogenesis of AHR.
气道高反应性(AHR)是支气管哮喘的一个关键组成部分,但其潜在机制仍有待揭示。我们目前的研究旨在建立一种新的良好的AHR实验动物模型。用DNP-蛔虫抗原(DNP-Asc)主动致敏的雄性Wistar大鼠在首次免疫后8天通过吸入DNP-Asc进行激发(单次抗原激发)。另一个致敏组每48小时接受3次激发(重复抗原激发)。在麻醉状态下测定气道对吸入乙酰胆碱(ACh)和神经激肽A(NKA)的反应性。还用伊文思蓝(E.B.)测定气道微血管渗漏情况。单次抗原激发后24小时,气道对ACh和NKA的反应性略有增强,主支气管中E.B.渗出增加。相比之下,重复抗原激发后24小时,气道对ACh和NKA的反应性以及主支气管中E.B.渗出明显增强。从激发大鼠分离出的主支气管条对ACh和5-羟色胺产生了AHR。这些发现表明,重复抗原激发在体内和体外均会导致明显的AHR,并且气道炎症可能与AHR的发病机制密切相关。