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首页> 外文期刊>Inhalation toxicology >Total and regional deposition of ultrafine particles in a mouse model of allergic inflammation of the lung.
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Total and regional deposition of ultrafine particles in a mouse model of allergic inflammation of the lung.

机译:在肺部过敏性炎症的小鼠模型中,超细颗粒的全部和局部沉积。

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摘要

Epidemiological studies have shown an association between ambient particle inhalation and adverse respiratory heath effects. Inhalation of ultrafine particles (UFP, diameter <100 nm) has been suggested to contribute to exacerbation of allergic airway inflammation. Here we analyze the potential effects of allergen sensitization and challenge on total and regional deposition of UFP in the lung. Ovalbumin (OVA)-sensitized and nonsensitized mice were exposed for 1 h to ultrafine iridium particles radiolabeled with (192)Ir (UF-Ir) (0.2 mg m(-3)) at 2 different time points either before or after allergen (OVA) challenge. Additional sensitized and nonsensitized mice were exposed to UF-Ir without allergen challenge. Lung total and regional UF-Ir deposition were calculated according to the distribution of radioactivity in the body and in the excreta during 3 days following UF-Ir inhalation. OVA-sensitized mice showed a 21% relative increase of total UF-Ir deposited fraction compared to nonsensitized mice. When UF-Ir inhalation was performed after allergen challenge, no difference in total UF-Ir deposited fraction between sensitized and nonsensitized mice was detectable. Furthermore, no differences in extrathoracic deposition or in regional particle deposition were detected between all experimental groups. This study indicates that allergen sensitization alone can affect UFP deposition in the lungs. Whether higher UFP deposition in sensitized individuals compared to nonsensitized individuals or whether other factors, like alterations in long-term clearance kinetics, contribute substantially to the susceptibility of allergic individuals to particle exposure has yet to be elucidated.
机译:流行病学研究表明,周围环境颗粒物吸入与不利的呼吸健康影响之间存在关联。已建议吸入超细颗粒(UFP,直径<100 nm)有助于加剧过敏性气道炎症。在这里,我们分析了变应原致敏和挑战对UFP在肺中的全部和区域沉积的潜在影响。将卵清蛋白(OVA)致敏和未致敏的小鼠在变应原(OVA)之前或之后的两个不同时间点暴露于用(192)Ir(UF-Ir)(0.2 mg m(-3))放射性标记的超细铱粒子中暴露1小时)挑战。将另外的致敏和未致敏小鼠暴露于UF-Ir,而没有过敏原攻击。根据UF-Ir吸入后3天内人体和排泄物中放射性的分布,计算肺总和区域UF-Ir的沉积。与未致敏小鼠相比,OVA致敏小鼠显示出总UF-Ir沉积分数的相对增加21%。当过敏原激发后进行UF-Ir吸入时,在敏化和未敏化小鼠之间未检测到总UF-Ir沉积分数的差异。此外,在所有实验组之间未检测到胸外沉积或区域颗粒沉积的差异。这项研究表明,单独的变应原致敏作用会影响UFP在肺中的沉积。尚不清楚在敏化个体中与未敏化个体相比更高的UFP沉积或其他因素(如长期清除动力学的改变)是否在很大程度上造成了过敏性个体对颗粒暴露的敏感性。

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