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N-乙酰天冬氨酰谷氨酸抑制变应原诱导的晚期鼻反应中的细胞募集和介质释放。

N-acetyl-aspartyl-glutamic acid inhibits cellular recruitment and mediator release during the late allergen-induced nasal reaction.

作者信息

Miadonna A, Milazzo N, Salmaso C, Cottini M, Lorini M, Tedeschi A

机构信息

Third Division of Internal Medicine, IRCCS Ospedale Maggiore Policlinico, Milan, Italy.

出版信息

Eur J Clin Pharmacol. 1998 Sep;54(7):515-20. doi: 10.1007/s002280050506.

DOI:10.1007/s002280050506
PMID:9832292
Abstract

OBJECTIVE

N-acetyl-aspartyl-glutamic acid (NAAGA) was effective in the treatment of allergic rhinitis, with an action on early allergen-induced nasal symptoms and mediator release. The aim of this study was to evaluate the clinical activity of NAAGA and its effects on the late antigen-induced reaction in the nose.

METHODS

Ten patients with allergic seasonal rhinitis were included in this randomized double-blind crossover trial of a 6% wt/vol solution of NAAGA (daily dosage 84 mg) versus placebo (lactose). The drug and placebo were administered intranasally five times daily for 1 week, with a 2-week interval between treatments.

RESULTS

Treatment with NAAGA, but not with placebo, significantly reduced the late antigen-induced nasal symptoms, mainly nasal obstruction. Eosinophil numbers in the nasal lavages collected 6 h and 24 h after challenge were significantly lower after NAAGA than after placebo. Active treatment also significantly reduced the neutrophil count 6 h after antigen challenge, and significantly lowered eosinophil cationic protein and myeloperoxidase levels in nasal lavages 6 h and 24 h after antigen challenge.

CONCLUSION

These results indicate that treatment for 1 week with NAAGA can reduce the late antigen-induced reaction in the nose. This is accompanied by a reduction in eosinophil and neutrophil recruitment and release of eosinophil cationic protein and myeloperoxidase.

摘要

目的

N - 乙酰 - 天冬氨酰 - 谷氨酸(NAAGA)对过敏性鼻炎有效,可作用于早期变应原诱导的鼻部症状及介质释放。本研究旨在评估NAAGA的临床活性及其对鼻部迟发性抗原诱导反应的影响。

方法

本随机双盲交叉试验纳入了10例季节性变应性鼻炎患者,对比6%重量/体积的NAAGA溶液(日剂量84毫克)与安慰剂(乳糖)。药物和安慰剂均经鼻给药,每日5次,持续1周,治疗间隔2周。

结果

使用NAAGA治疗可显著减轻迟发性抗原诱导的鼻部症状,主要是鼻塞,而安慰剂则无此效果。激发后6小时和24小时采集的鼻灌洗液中的嗜酸性粒细胞数量,NAAGA治疗组显著低于安慰剂组。积极治疗还可显著降低抗原激发后6小时的中性粒细胞计数,并显著降低抗原激发后6小时和24小时鼻灌洗液中嗜酸性粒细胞阳离子蛋白和髓过氧化物酶水平。

结论

这些结果表明,NAAGA治疗1周可减轻鼻部迟发性抗原诱导的反应。这伴随着嗜酸性粒细胞和中性粒细胞募集减少,以及嗜酸性粒细胞阳离子蛋白和髓过氧化物酶释放减少。

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