Establishment of particulate matter-induced lung injury model in mouse.

IF 2.7 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Laboratory Animal Research Pub Date : 2021-07-30 DOI:10.1186/s42826-021-00097-x
Se Yong Park, Kyu Sup An, Buhyun Lee, Ju-Hee Kang, Hyun Jin Jung, Min Woo Kim, Hyeon Yeol Ryu, Kyu-Suk Shim, Ki Taek Nam, Yeo Sung Yoon, Seung Hyun Oh
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引用次数: 5

Abstract

Background: Particulate matter (PM) is one of the principal causes of human respiratory disabilities resulting from air pollution. Animal models have been applied to discover preventive and therapeutic drugs for lung diseases caused by PM. However, the induced severity of lung injury in animal models using PM varies from study to study due to disparities in the preparation of PM, and the route and number of PM administrations. In this study, we established an in vivo model to evaluate PM-induced lung injury in mice.

Results: PM dispersion was prepared using SRM2975. Reactive oxygen species were increased in MLE 12 cells exposed to this PM dispersion. In vivo studies were conducted in the PM single challenge model, PM multiple challenge model, and PM challenge with ovalbumin-induced asthma using the PM dispersion. No histopathological changes were observed in lung tissues after a single injection of PM, whereas mild to moderate lung inflammation was obtained in the lungs of mice exposed to PM three times. However, fibrotic changes were barely seen, even though transmission electron microscopy (TEM) studies revealed the presence of PM particles in the alveolar macrophages and alveolar capillaries. In the OVA-PM model, peribronchial inflammation and mucous hypersecretion were more severe in the OVA+PM group than the OVA group. Serum IgE levels tended to increase in OVA+PM group than in OVA group.

Conclusions: In this study, we established a PM-induced lung injury model to examine the lung damage induced by PM. Based on our results, repeated exposures of PM are necessary to induce lung inflammation by PM alone. PM challenge, in the presence of underlying diseases such as asthma, can also be an appropriate model for studying the health effect of PM.

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小鼠颗粒性肺损伤模型的建立。
背景:颗粒物(PM)是空气污染导致人类呼吸功能障碍的主要原因之一。动物模型已被用于发现PM引起的肺部疾病的预防和治疗药物。然而,由于PM的制备方法、给药途径和给药次数的差异,PM在动物模型中诱导的肺损伤严重程度因研究而异。在这项研究中,我们建立了一个体内模型来评估pm引起的小鼠肺损伤。结果:用SRM2975制备了PM分散体。暴露于PM分散体的MLE 12细胞中活性氧增加。体内研究分别采用PM单次攻击模型、PM多次攻击模型和PM分散体对卵清蛋白诱导哮喘的PM攻击。单次注射PM后,肺组织未见组织病理学改变,而三次注射PM后,小鼠肺部出现轻度至中度炎症。然而,尽管透射电镜(TEM)研究显示肺泡巨噬细胞和肺泡毛细血管中存在PM颗粒,但纤维化变化几乎未见。在OVA-PM模型中,OVA+PM组支气管周围炎症和粘液高分泌比OVA组更严重。血清IgE水平在OVA+PM组较OVA组有升高的趋势。结论:本研究建立PM致肺损伤模型,检测PM致肺损伤。根据我们的研究结果,反复暴露于PM是必要的,以单独诱导PM肺部炎症。在存在诸如哮喘等潜在疾病的情况下,PM挑战也可以作为研究PM对健康影响的适当模型。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
32
审稿时长
8 weeks
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