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长期暴露于柴油废气颗粒会导致小鼠肺泡增大。

Chronic exposure of diesel exhaust particles induces alveolar enlargement in mice.

作者信息

Yoshizaki Kelly, Brito Jôse Mára, Moriya Henrique T, Toledo Alessandra C, Ferzilan Sandra, Ligeiro de Oliveira Ana Paula, Machado Isabel D, Farsky Sandra H P, Silva Luiz F F, Martins Milton A, Saldiva Paulo H N, Mauad Thais, Macchione Mariangela

出版信息

Respir Res. 2015 Feb 7;16(1):18. doi: 10.1186/s12931-015-0172-z.

Abstract

BACKGROUND

Diesel exhaust particles (DEPs) are deposited into the respiratory tract and are thought to be a risk factor for the development of diseases of the respiratory system. In healthy individuals, the timing and mechanisms of respiratory tract injuries caused by chronic exposure to air pollution remain to be clarified.

METHODS

We evaluated the effects of chronic exposure to DEP at doses below those found in a typical bus corridor in Sao Paulo (150 μg/m3). Male BALB/c mice were divided into mice receiving a nasal instillation: saline (saline; n = 30) and 30 μg/10 μL of DEP (DEP; n = 30). Nasal instillations were performed five days a week, over a period of 90 days. Bronchoalveolar lavage (BAL) was performed, and the concentrations of interleukin (IL)-4, IL-10, IL-13 and interferon-gamma (INF-γ) were determined by ELISA-immunoassay. Assessment of respiratory mechanics was performed. The gene expression of Muc5ac in lung was evaluated by RT-PCR. The presence of IL-13, MAC2+ macrophages, CD3+, CD4+, CD8+ T cells and CD20+ B cells in tissues was analysed by immunohistochemistry. Bronchial thickness and the collagen/elastic fibers density were evaluated by morphometry. We measured the mean linear intercept (Lm), a measure of alveolar distension, and the mean airspace diameter (D0) and statistical distribution (D2).

RESULTS

DEP decreased IFN-γ levels in BAL (p = 0.03), but did not significantly alter IL-4, IL-10 and IL-13 levels. MAC2+ macrophage, CD4+ T cell and CD20+ B cell numbers were not altered; however, numbers of CD3+ T cells (p ≤ 0.001) and CD8+ T cells (p ≤ 0.001) increased in the parenchyma. Although IL-13 (p = 0.008) expression decreased in the bronchiolar epithelium, Muc5ac gene expression was not altered in the lung of DEP-exposed animals. Although respiratory mechanics, elastic and collagen density were not modified, the mean linear intercept (Lm) was increased in the DEP-exposed animals (p ≤ 0.001), and the index D2 was statistically different (p = 0.038) from the control animals.

CONCLUSION

Our data suggest that nasal instillation of low doses of DEP over a period of 90 days results in alveolar enlargement in the pulmonary parenchyma of healthy mice.

摘要

背景

柴油尾气颗粒(DEPs)沉积于呼吸道,被认为是呼吸系统疾病发生的一个风险因素。在健康个体中,长期暴露于空气污染所导致的呼吸道损伤的时间和机制仍有待阐明。

方法

我们评估了低于圣保罗典型公交走廊中发现的剂量(150μg/m³)的长期暴露于DEP的影响。雄性BALB/c小鼠被分为接受滴鼻的小鼠:生理盐水(生理盐水组;n = 30)和30μg/10μL的DEP(DEP组;n = 30)。每周进行5天滴鼻,持续90天。进行支气管肺泡灌洗(BAL),并通过ELISA免疫测定法测定白细胞介素(IL)-4、IL-10、IL-13和干扰素-γ(INF-γ)的浓度。进行呼吸力学评估。通过RT-PCR评估肺中Muc5ac的基因表达。通过免疫组织化学分析组织中IL-13、MAC2+巨噬细胞、CD3+、CD4+、CD8+ T细胞和CD20+ B细胞的存在情况。通过形态计量学评估支气管厚度和胶原/弹性纤维密度。我们测量了平均线性截距(Lm),这是肺泡扩张的一种度量,以及平均气腔直径(D0)和统计分布(D2)。

结果

DEP降低了BAL中的IFN-γ水平(p = 0.03),但未显著改变IL-4、IL-10和IL-13水平。MAC2+巨噬细胞、CD4+ T细胞和CD20+ B细胞的数量未改变;然而,实质中CD3+ T细胞(p≤0.001)和CD8+ T细胞(p≤0.001)的数量增加。尽管细支气管上皮中IL-13(p = 0.008)表达降低,但DEP暴露动物肺中的Muc5ac基因表达未改变。尽管呼吸力学、弹性和胶原密度未改变,但DEP暴露动物的平均线性截距(Lm)增加(p≤0.001),并且指数D2与对照动物在统计学上有差异(p = 0.038)。

结论

我们的数据表明,在90天内对健康小鼠进行低剂量DEP滴鼻会导致肺实质中的肺泡扩大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1b/4345004/8e8cb1c05b0c/12931_2015_172_Fig1_HTML.jpg

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