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阿昔洛韦对阿司匹林诱发哮喘患者支气管收缩及尿白三烯E4排泄的影响。

Effect of acyclovir on bronchoconstriction and urinary leukotriene E4 excretion in aspirin-induced asthma.

作者信息

Yoshida S, Sakamoto H, Yamawaki Y, Shoji T, Akahori K, Onuma K, Nakagawa H, Hasegawa H, Amayasu H

机构信息

Institute for Medical Sciences, Fujita Health University School of Medicine, Toyoake, Japan.

出版信息

J Allergy Clin Immunol. 1998 Dec;102(6 Pt 1):909-14. doi: 10.1016/s0091-6749(98)70327-6.

Abstract

BACKGROUND

Acyclovir (9-[2-hydroxyethoxymethyl] guanine), an inhibitor of the DNA polymerase of the herpes virus, has been reported to exhibit pharmacologic activity other than antiviral activity, including antiasthmatic effects.

OBJECTIVE

This study was designed to investigate the protective effect of acyclovir on airway responsiveness to the sulpyrine provocation test and to investigate whether this protective activity is associated with a reduction in aspirin-induced excretion of urinary leukotriene E4 (u-LTE4 ), a marker of cysteinyl leukotriene (LT) overproduction that participates in the pathogenesis of aspirin-induced asthma.

METHODS

We assessed the effects of pretreatment with acyclovir on bronchoconstriction precipitated by inhalation of sulpyrine in 16 adult patients with mild or moderate aspirin-induced asthma; those who were in stable clinical condition and were hyperresponsive to the sulpyrine provocation test were allocated to this study. A double-blind, randomized, cross-over design was used. u-LTE4 was measured by a combined reverse-phase HPLC enzyme immunoassay.

RESULTS

Acyclovir protects against aspirin-induced attacks of asthma through mechanisms unrelated to its bronchodilator property but related to the improvement of bronchial hypersensitivity to sulpyrine; protection was nearly complete in all patients (P <.0001). By contrast, after acyclovir, the maximum level of u-LTE4 in patients was significantly lower than that in control subjects (P <. 01).

CONCLUSION

Our results suggest that acyclovir is not only an antiviral drug but also an inhibitor of analgesic-induced bronchoconstriction, probably acting by inhibiting the release of cysteinyl LTs.

摘要

背景

阿昔洛韦(9-[2-羟乙氧甲基]鸟嘌呤)是一种疱疹病毒DNA聚合酶抑制剂,据报道它具有除抗病毒活性以外的药理活性,包括抗哮喘作用。

目的

本研究旨在探讨阿昔洛韦对气道反应性在舒必利激发试验中的保护作用,并研究这种保护活性是否与阿司匹林诱导的尿白三烯E4(u-LTE4)排泄减少有关,u-LTE4是半胱氨酰白三烯(LT)产生过多的标志物,参与阿司匹林诱发哮喘的发病机制。

方法

我们评估了16例轻度或中度阿司匹林诱发哮喘的成年患者,在吸入舒必利诱发支气管收缩前使用阿昔洛韦预处理的效果;将那些临床状况稳定且对舒必利激发试验反应过度的患者纳入本研究。采用双盲、随机、交叉设计。通过反相高效液相色谱酶联免疫分析法联合测定u-LTE4。

结果

阿昔洛韦通过与其支气管扩张特性无关但与改善支气管对舒必利的高反应性有关的机制,预防阿司匹林诱发的哮喘发作;在所有患者中保护作用几乎是完全的(P<.0001)。相比之下,使用阿昔洛韦后,患者的u-LTE4最高水平显著低于对照组(P<.01)。

结论

我们的结果表明,阿昔洛韦不仅是一种抗病毒药物,也是一种镇痛诱导支气管收缩的抑制剂,可能通过抑制半胱氨酰白三烯的释放发挥作用。

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