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磷酸二酯酶4和1抑制剂KF19514经吸入给药可预防豚鼠抗原诱导的肺部炎症。

The inhaled administration of KF19514, a phosphodiesterase 4 and 1 inhibitor, prevents antigen-induced lung inflammation in guinea pigs.

作者信息

Manabe H, Akuta K, Kawasaki H, Ohmori K

机构信息

Pharmaceutical Research Institute, Kyowa Hakko Kogyo Co. Ltd, 1188 Shimotogari, Nagaizumi-cho, Sunto-gun, Shizuoka, 411, Japan.

出版信息

Pulm Pharmacol Ther. 2000;13(1):5-11. doi: 10.1006/pupt.1999.0224.

DOI:10.1006/pupt.1999.0224
PMID:10718985
Abstract

We examined in this study the effect of KF19514, a phosphodiesterase 4 and 1 inhibitor, on antigen-induced lung inflammation by inhaled administration in guinea-pigs. It was previously reported that inhaled KF19514 prevented antigen-induced bronchoconstriction and platelet-activating factor (PAF)-induced lung inflammation. In fact, a variety of factors other than PAF are related to lung inflammation in real subjects with asthma. Guinea-pigs were actively sensitized by exposure to ovalbumin (OA). Fifteen to 20 days later, the guinea pigs were challenged by exposure to aerosols of five successively increasing concentrations of OA (0.01, 0.1, 0.5, 1 and 5 mg/ml). Bronchoalveolar lavages (BALs) were performed 24 h after the antigen challenge, and airway hyperresponsiveness to acetylcholine (ACh) was studied 24 h after the challenge by measuring lung resistance and dynamic compliance. Ovalbumin antigen challenge produced a marked and significant eosinophil accumulation in the BAL fluids and airway hyperresponsiveness to ACh 24 h after the challenge. Inhaled KF19514 (0.01-0.1%) inhibited the eosinophil accumulation significantly and dose-dependently but inhaled rolipram (0.01-0.1%) and aminophylline (0.1-1%) did not. In addition, the development of airway hyperresponsiveness was prevented by inhaled KF19514 (0.01%) but not by inhaled rolipram (0.01%) and aminophylline (0.1%). Based on these data, KF19514 was suggested to be a promising drug in the treatment of asthma by local administration to the lung.

摘要

在本研究中,我们通过对豚鼠进行吸入给药,研究了磷酸二酯酶4和1抑制剂KF19514对抗原诱导的肺部炎症的影响。此前有报道称,吸入KF19514可预防抗原诱导的支气管收缩和血小板活化因子(PAF)诱导的肺部炎症。事实上,在实际的哮喘患者中,除PAF外,还有多种因素与肺部炎症有关。豚鼠通过接触卵清蛋白(OA)进行主动致敏。15至20天后,对豚鼠依次吸入浓度递增的五种OA气雾剂(0.01、0.1、0.5、1和5 mg/ml)进行激发。抗原激发24小时后进行支气管肺泡灌洗(BAL),激发24小时后通过测量肺阻力和动态顺应性研究气道对乙酰胆碱(ACh)的高反应性。卵清蛋白抗原激发在激发后24小时导致BAL液中明显且显著的嗜酸性粒细胞积聚以及气道对ACh的高反应性。吸入KF19514(0.01 - 0.1%)可显著且剂量依赖性地抑制嗜酸性粒细胞积聚,但吸入咯利普兰(0.01 - 0.1%)和氨茶碱(0.1 - 1%)则无此作用。此外,吸入KF19514(0.01%)可预防气道高反应性的发展,但吸入咯利普兰(0.01%)和氨茶碱(0.1%)则不能。基于这些数据,KF19514被认为是一种通过肺部局部给药治疗哮喘的有前景的药物。

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