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致敏和变应原激发后棕色挪威大鼠肺中诱导型一氧化氮合酶的变化

Inducible nitric oxide synthase after sensitization and allergen challenge of Brown Norway rat lung.

作者信息

Liu S F, Haddad E B, Adcock I, Salmon M, Koto H, Gilbey T, Barnes P J, Chung K F

机构信息

National Heart and Lung Institute, Imperial College School of Medicine, London.

出版信息

Br J Pharmacol. 1997 Aug;121(7):1241-6. doi: 10.1038/sj.bjp.0701242.

Abstract
  1. We studied the effects of ovalbumin (OA) sensitization and challenge on inducible nitric oxide synthase (iNOS) gene and protein expression in Brown-Norway rats in vivo. 2. By use of Northern analysis, a 4.4-kb iNOS mRNA transcript was weakly observed in control rat lung but there was a 3 fold increase in lungs sensitized to OA alone (P<0.05). In sensitized rats, four hours after exposure to OA aerosol, there was a 6 fold increase in iNOS mRNA transcript (P<0.05), which returned to baseline at 24 h. 3. Immunostaining with an anti-mouse iNOS antibody revealed some patchy staining of airway epithelium in naive rats. There were no changes in sensitized rats exposed to saline, but sensitized and OA-exposed rats showed increased expression in iNOS staining in macrophages. 4. Electrophoretic mobility shift assays of lung nuclear extracts showed a marked increase in nuclear factor-kappaB (NF-kappaB)-binding activity at 2 h after allergen exposure with return to baseline at 6, 12 and 24 h. 5. We concluded that there is increased iNOS gene and protein expression associated with increased NF-kappaB DNA-binding in lungs of sensitized and challenged rats. The increase in iNOS expression may underlie the increase in exhaled NO found after allergen challenge and may contribute to the development of allergen-induced airway hyperresponsiveness.
摘要
  1. 我们在体内研究了卵清蛋白(OA)致敏和激发对Brown-Norway大鼠诱导型一氧化氮合酶(iNOS)基因及蛋白表达的影响。2. 通过Northern分析,在对照大鼠肺中微弱观察到一条4.4 kb的iNOS mRNA转录本,但仅对OA致敏的大鼠肺中该转录本增加了3倍(P<0.05)。在致敏大鼠中,暴露于OA气雾剂4小时后,iNOS mRNA转录本增加了6倍(P<0.05),并在24小时恢复至基线水平。3. 用抗小鼠iNOS抗体进行免疫染色显示,未致敏大鼠气道上皮有一些斑片状染色。暴露于生理盐水的致敏大鼠无变化,但致敏并暴露于OA的大鼠巨噬细胞中iNOS染色表达增加。4. 肺核提取物的电泳迁移率变动分析显示,变应原暴露后2小时核因子κB(NF-κB)结合活性显著增加,并在6、12和24小时恢复至基线水平。5. 我们得出结论,致敏和激发大鼠肺中iNOS基因及蛋白表达增加与NF-κB DNA结合增加相关。iNOS表达的增加可能是变应原激发后呼出NO增加的基础,并可能有助于变应原诱导的气道高反应性的发展。

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