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福莫特罗与莫米松在小鼠过敏性肺部炎症模型中的协同作用。

Synergistic effect of formoterol and mometasone in a mouse model of allergic lung inflammation.

作者信息

Wyss D, Bonneau O, Trifilieff A

机构信息

Respiratory Diseases Area, Novartis Institute for BioMedical Research, CH-4002 Basel, Switzerland.

出版信息

Br J Pharmacol. 2007 Sep;152(1):83-90. doi: 10.1038/sj.bjp.0707381. Epub 2007 Jul 9.

Abstract

BACKGROUND AND PURPOSE

Controversy still exists as to whether or not inhaled beta (2)-adrenoceptor agonists and corticosteroids act synergistically in vivo. In this study, we have used a murine model of lung inflammation to study the synergistic effect of an inhaled beta (2)-adrenoceptor agonist (formoterol) and an inhaled corticosteroid (mometasone).

EXPERIMENTAL APPROACH

Actively sensitized mice were challenged with aerosolized ovalbumin, once a day, for three consecutive days. Three days after the last of the three challenges, a final allergen challenge was given. Allergen-induced increase in Penh was measured 4 h after the last challenge. A day after the last challenge, increased airway sensitivity to aerosolized methacholine was demonstrated and this was concomitant with an influx of inflammatory cells in the bronchoalveolar lavage fluids.

KEY RESULTS

Mometasone (0.1 to 3 mg kg(-1)) given intranasally either an hour before or after the last allergen challenge, dose-dependently inhibited all parameters. When given intranasally either one or three hours after the last allergen challenge, but not an hour before, formoterol (1.5 to 150 microg kg(-1)) also dose-dependently inhibited most of the parameters to different degree. A synergistic effect on the allergen-induced increase in Penh was demonstrated for mometasone and formoterol given in combination, an hour after the challenge, at the following doses: mometasone/formoterol (in microg kg(-1)) 1/10, 1/100, 5/10, and 5/100.

CONCLUSIONS AND IMPLICATIONS

Our results support the hypothesis that when given as a fixed combination, inhaled corticosteroid and beta (2)-adrenoceptor agonist act synergistically in vivo.

摘要

背景与目的

吸入性β₂肾上腺素受体激动剂和皮质类固醇在体内是否协同作用仍存在争议。在本研究中,我们使用小鼠肺部炎症模型来研究吸入性β₂肾上腺素受体激动剂(福莫特罗)和吸入性皮质类固醇(莫米松)的协同作用。

实验方法

对主动致敏的小鼠连续三天每天进行雾化卵清蛋白激发。在三次激发中的最后一次激发后三天,进行最终的过敏原激发。在最后一次激发后4小时测量过敏原诱导的Penh增加。在最后一次激发后一天,证明气道对雾化乙酰甲胆碱的敏感性增加,这与支气管肺泡灌洗液中炎症细胞的流入同时发生。

关键结果

在最后一次过敏原激发前或后一小时鼻内给予莫米松(0.1至3mg kg⁻¹),剂量依赖性地抑制所有参数。在最后一次过敏原激发后1或3小时但不是前一小时鼻内给予时,福莫特罗(1.5至150μg kg⁻¹)也不同程度地剂量依赖性地抑制大多数参数。在激发后一小时,以以下剂量联合给予莫米松和福莫特罗时,对过敏原诱导的Penh增加显示出协同作用:莫米松/福莫特罗(以μg kg⁻¹计)1/10、1/100、5/10和5/100。

结论与启示

我们的结果支持以下假设,即当以固定组合给药时,吸入性皮质类固醇和β₂肾上腺素受体激动剂在体内协同作用。

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