首页> 外文期刊>Inflammation research: Official journal of the European Histamine Research Society >Intra-luminal exposure of murine airways to peroxynitrite causes inflammation but not hyperresponsiveness.
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Intra-luminal exposure of murine airways to peroxynitrite causes inflammation but not hyperresponsiveness.

机译:鼠气管腔内暴露于过亚硝酸盐会引起炎症,但不会引起高反应性。

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摘要

OBJECTIVE AND DESIGN: There is increasing evidence for the involvement of reactive nitrogen species like peroxynitrite (ONOO-) in airway pathology, for example during allergic airway inflammation. Therefore, the effect of peroxynitrite exposure on airway responsiveness and inflammation was studied. MATERIALS: Male BALB/c mice were treated intra-tracheally with authentic peroxynitrite and the peroxynitrite donor 3-morpholinosydnonimine (SIN-1). Control animals received decomposed solutions of peroxynitrite and SIN- 1. METHODS: Airway inflammation was monitored by bronchoalveolar lavage, three and seven days after administration. Airway responsiveness to methacholine and acetylcholine was measured on day 1, 2, 3 and 7 post administration using whole body plethysmography. RESULTS: Intra-tracheal administration of peroxynitrite 200 microM in 50 microl phosphate buffered saline (PBS) induced a significant increase in macrophages (>35%, p < 0.05) in the airway lumen three days after administration. In contrast, neither intra-tracheal administration of authentic peroxynitrite (up to 5 mM) nor the peroxynitrite donor SIN-1 (1 mM, both intra-tracheal and nebulized) changed airway responsiveness to methacholine. Moreover, peroxynitrite (5 mM) did not alter responsiveness to acetylcholine. CONCLUSION: Administration of peroxynitrite directly into the airways of BALB/c mice, induces airway inflammation, but not airway hyperresponsiveness. It is suggested that antioxidants in the epithelial lining fluid and/or the epithelium itself form an efficient barrier, which prevents peroxynitrite from reaching putative targets in the airway interstitium.
机译:目的和设计:越来越多的证据表明反应性氮物质(如过氧亚硝酸盐(ONOO-))参与气道病理,例如在过敏性气道炎症期间。因此,研究了过亚硝酸盐暴露对气道反应性和炎症的影响。材料:雄性BALB / c小鼠经气管内用正过氧亚硝酸盐和过氧亚硝酸盐供体3-吗啉代亚砜亚胺(SIN-1)进行治疗。对照组动物接受过氧亚硝酸盐和SIN-1分解后的溶液。方法:给药后三天和七天,通过支气管肺泡灌洗监测气道炎症。使用全身体积描记法在给药后第1、2、3和7天测量气道对乙酰甲胆碱和乙酰胆碱的反应性。结果:气管内给予过氧亚硝酸盐在50微升磷酸盐缓冲盐水(PBS)中的200 microM气管内给药后三天引起气管腔巨噬细胞显着增加(> 35%,p <0.05)。相反,气管内施用真正的过氧亚硝酸盐(最高5 mM)或过氧亚硝酸盐供体SIN-1(1 mM,气管内和雾化)均未改变气道对乙酰甲胆碱的反应性。而且,过氧亚硝酸盐(5 mM)不会改变对乙酰胆碱的反应性。结论:过氧亚硝酸盐直接进入BALB / c小鼠气道可引起气道炎症,但不会引起气道高反应性。提示上皮内衬液和/或上皮本身中的抗氧化剂形成有效的屏障,从而防止过氧亚硝酸盐到达气道间质中假定的靶标。

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