首页> 外文期刊>Toxicology and Applied Pharmacology >Inhalation of diesel exhaust enhances allergen-related eosinophil recruitment and airway hyperresponsiveness in mice.
【24h】

Inhalation of diesel exhaust enhances allergen-related eosinophil recruitment and airway hyperresponsiveness in mice.

机译:吸入柴油机废气会增强小鼠变应原相关的嗜酸性粒细胞募集和气道高反应性。

获取原文
获取原文并翻译 | 示例
           

摘要

We have previously shown that intratracheal instillation of suspension of diesel exhaust particles enhances allergen-related eosinophilic airway inflammation, airway hyperresponsiveness, and local expression of interleukin (IL)-5 and granulocyte macrophage-colony stimulating factor (GM-CSF) in mice. The present study was designed to elucidate the effects of daily inhalation of diesel exhaust (DE) on the allergen-related respiratory disease. ICR mice were exposed for 40 weeks to clean air or DE at a soot concentration of 0.3, 1.0, or 3.0 mg/m3 with aerosol allergen challenges (1% ovalbumin in isotonic saline for 6 min) at 3-week intervals during the last 24 weeks of exposures. Exposure to DE enhanced allergen-related eosinophil recruitment to the submucosal layers of the airways and to the bronchoalveolar space, and increased protein levels of GM-CSF and IL-5 in the lung in a dose-dependent manner compared to exposure to clean air. There were strong correlations between the number of eosinophils in bronchoalveolar lavage (BAL) fluid and IL-5 concentrations in BAL supernatants and lung tissue supernatants. In addition, the increases in eosinophil recruitment and local cytokine expression were accompanied by goblet cell proliferation in the bronchial epithelium and airway hyperresponsiveness to inhaled acetylcholine. In contrast, the control mice exposed for 40 weeks to clean air or DE at a soot concentration of 0.3, 1.0, or 3.0 mg/m3 without allergen provocation showed no eosinophil recruitment to the submucosal layers of the airways nor to the bronchoalveolar space and few goblet cells in the bronchial epithelium. The present study provides experimental evidence that daily inhalation of DE can enhance allergen-related respiratory diseases such as allergic asthma. This effect may be mediated by the enhanced local expression of IL-5 and GM-CSF. Increased ambient levels of DE may be implicated in the increasing prevalence of bronchial asthma in recent years.
机译:我们以前已经表明,气管内滴注柴油机排气颗粒的悬浮液可增强变应原相关的嗜酸性气道炎症,气道高反应性以及小鼠中白介素(IL)-5和粒细胞巨噬细胞集落刺激因子(GM-CSF)的局部表达。本研究旨在阐明每日吸入柴油机废气(DE)对与变应原相关的呼吸系统疾病的影响。在最后24小时内,每隔3周将ICR小鼠暴露在空气中,烟尘浓度为0.3、1.0或3.0 mg / m3的烟尘浓度为0.3、1.0或3.0 mg / m3的清洁空气或DE(等渗盐水中1%卵清蛋白6分钟)。数周的曝光。与暴露于清洁空气相比,暴露于DE可以增强剂量相关的变应原相关嗜酸性粒细胞募集至气道粘膜下层和支气管肺泡空间,并增加肺中GM-CSF和IL-5的蛋白质​​水平。支气管肺泡灌洗(BAL)液中嗜酸性粒细胞的数量与BAL上清液和肺组织上清液中IL-5浓度之间存在很强的相关性。此外,嗜酸性粒细胞募集和局部细胞因子表达的增加伴随着杯状细胞在支气管上皮中的增殖以及气道对吸入乙酰胆碱的高反应性。相比之下,对照组小鼠暴露于烟尘浓度为0.3、1.0或3.0 mg / m3的清洁空气或DE中,但未引起过敏原的情况下,暴露40周后,没有嗜酸性粒细胞募集到气道粘膜下层或支气管肺泡间隙,几乎没有支气管上皮中的杯状细胞。本研究提供实验证据,每天吸入DE可以增强与变应原有关的呼吸系统疾病,例如过敏性哮喘。 IL-5和GM-CSF的局部表达增强可能介导了这种作用。近年来,DE的环境水平升高可能与支气管哮喘的患病率增加有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号