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Comparison of the Pulmonary Oxidative Stress Caused by Intratracheal Instillation and Inhalation of NiO Nanoparticles when Equivalent Amounts of NiO Are Retained in the Lung

机译:当在肺中保留等效量的NiO时,通过气管内滴注和吸入NiO纳米颗粒引起的肺氧化应激的比较

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NiO nanoparticles were administered to rat lungs via intratracheal instillation or inhalation. During pulmonary toxicity caused by NiO nanoparticles, the induction of oxidative stress is a major factor. Both intratracheal instillation and inhalation of NiO nanoparticles induced pulmonary oxidative stress. The oxidative stress response protein, heme oxygenase-1 (HO-1), was induced by the administration of NiO nanoparticles at both the protein and gene expression level. Additionally, certain oxidative-stress markers in the lung, such as 8-iso-prostaglandin F2α, thioredoxin, and inducible nitric oxide synthase were increased. Furthermore, the concentration of myeloperoxidase (MPO) in the lung was also increased by the administration of NiO nanoparticles. When the amount of NiO in the lung is similar, the responses against pulmonary oxidative stress of intratracheal instillation and inhalation are also similar. However, the state of pulmonary oxidative stress in the early phase was different between intratracheal instillation and inhalation, even if the amount of NiO in the lung was similar. Inhalation causes milder oxidative stress than that caused by intratracheal instillation. On evaluation of the nanoparticle-induced pulmonary oxidative stress in the early phase, we should understand the different states of oxidative stress induced by intratracheal instillation and inhalation.
机译:通过气管内滴注或吸入法将NiO纳米颗粒施用于大鼠肺。在由NiO纳米颗粒引起的肺毒性过程中,氧化应激的诱导是主要因素。气管内滴注和吸入NiO纳米颗粒均引起肺氧化应激。氧化应激反应蛋白血红素加氧酶-1(HO-1),是通过在蛋白质和基因表达水平上施用纳米氧化镍诱导的。此外,肺中某些氧化应激标记物,例如8-异前列腺素F2α,硫氧还蛋白和诱导型一氧化氮合酶也增加了。此外,通过施用NiO纳米颗粒也增加了肺中髓过氧化物酶(MPO)的浓度。当肺中的NiO量相似时,气管内滴注和吸入对肺氧化应激的反应也相似。但是,即使在肺中的NiO量相似,气管内滴注和吸入之间早期的肺氧化应激状态也不同。与气管内滴注相比,吸入引起的氧化应激更轻。在评估早期纳米颗粒引起的肺氧化应激时,我们应该了解气管内滴注和吸入引起的氧化应激的不同状态。

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