Effects of dexamethasone on leukotriene synthesis and airway responses to antigen and leukotriene D4 in rats.

医学 卵清蛋白 地塞米松 白三烯 白三烯D4 内科学 抗原 白三烯C4 气道阻力 内分泌学 体内 支气管收缩 免疫学 哮喘 生物 生物技术
作者
William S. Powell,L J Xu,James G. Martin
出处
期刊:American Journal of Respiratory and Critical Care Medicine [American Thoracic Society]
卷期号:151 (4): 1143-1150 被引量:9
标识
DOI:10.1164/ajrccm.151.4.7697244
摘要

Cysteinyl-leukotrienes (cysteinyl-LTs) are important mediators of both early and late allergen-induced airway responses in atopic asthmatics. We have investigated the effects of glucocorticoids on the in vivo synthesis of cysteinyl-LTs and airway responses to these mediators. Ovalbumin (OA)-sensitized Brown Norway rats, which exhibit early responses and, in most cases, also late responses to late antigen challenge, were treated with either one dose (1 h before antigen challenge) or two doses (2 and 14 h before challenge) of dexamethasone (dex; 300 micrograms/kg). A third group of sensitized rats which did not receive dex served as control animals. All rats were subjected to bile duct cannulation and tracheal intubation 2 h before intratracheal instillation of OA. All of the OA-treated control rats had pronounced early responses (5.5 +/- 1.0 times baseline pulmonary resistance [RL]), whereas 5 of 7 rats had late responses. Biliary levels of N-acetyl-LTE4 increased in all control rats following antigen challenge with a maximum occurring between 1 to 2 h, followed by a decline. There appeared to be a second maximum between 6 to 7 h after challenge, although this could not be demonstrated statistically because of the variability in the response among animals. Treatment with two doses of dex reduced the early response by 57%, completely eliminated the late response, and reduced the levels of N-acetyl-LTE4 in bile by about 80% at all time points.(ABSTRACT TRUNCATED AT 250 WORDS)
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