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[纳米氧化铟锡诱导大鼠铟肺疾病模型的建立及其病理特征探讨]

[Establishment of Nano-ITO induced rat model of indium lung disease and exploration of its pathological characteristics].

作者信息

Qu X Y, Li W K, Zhao Y Z, Lin Y Q, Li X R, Chen X Y, Guan Y, Yu Y, Xue L, Liu N

机构信息

School of Public Health, North China University of Science and Technology, Hebei Key Laboratory of Occupational Health and Safety for Coal Industry, Tangshan 063210, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2024 Sep 12;47(9):815-826. doi: 10.3760/cma.j.cn112147-20240311-00138.

Abstract

To study the dynamic pathological characteristics of lung tissue in a Nano-ITO induced rat model of indium lung disease and to guide clinical and basic scientific research to further explore the mechanisms of pulmonary interstitial injury and pulmonary alveolar proteinosis (PAP). Dose-response (three divided doses) and time-course studies (six exposure periods) were performed to investigate the pulmonary toxicity induced by Nano-ITO. At the end of the experiment, cytokine levels and oxidative stress were analyzed in the bronchoalveolar lavage fluid. Rat lung tissues were also collected for staining with H&E, PAS, Masson's, Oil Red O, and Sirius Red. Ultrastructure of lung tissue cells was observed by transmission electron microscopy. Expression of IL-1β, HO-1, SP-A was observed by immunohistochemistry, and the expression of α-SMA was observed by immunofluorescence. Nano-ITO intratracheal instillation caused pulmonary toxicity by inducing acute inflammation at 3 days, granuloma (nodule) formation and collagen hyperplasia at 14 days, and alveolar proteinosis at 56 days post-exposure. Pathological features of lung tissue included typical alveolar exudates, cellular fibrous nodules, enlarged alveolar fat droplet fusion, cholesterol crystal granuloma and pulmonary alveolar proteinosis. The intra-alveolar eosinophilic material (multilamellated, lattice-shaped, and myelin-like structure) showed abnormal lamellar bodies (features of alveolar type Ⅱ epithelial cells) and abundant rough endoplasmic reticulum and mitochondria (features of fibroblasts) on transmission electron microscopy of the lung tissue from rats exposed to Nano-ITO on the 84th day. Cellular pathology revealed that a large amount of amorphous PAS stain-positive substances appear in BALF at 28 days post-exposure, and pink granular protein-like substances can be seen in alveolar macrophages. There are three characteristic developmental stages in Nano-ITO induced pulmonary injury in rats, acute inflammation, granuloma (nodule) formation and collagen proliferation, and pulmonary alveolar proteinosis, which provide a reference feature model for the pathogenesis of indium lung disease.

摘要

研究纳米氧化铟锡诱导的大鼠铟肺疾病模型肺组织的动态病理特征,为临床和基础科研进一步探索肺间质损伤及肺泡蛋白沉积症(PAP)的发病机制提供指导。进行剂量反应(分三次给药)和时间进程研究(六个暴露时间段)以探讨纳米氧化铟锡诱导的肺毒性。实验结束时,分析支气管肺泡灌洗液中的细胞因子水平和氧化应激。同时收集大鼠肺组织进行苏木精-伊红(H&E)、过碘酸雪夫(PAS)、Masson氏、油红O和天狼星红染色。通过透射电子显微镜观察肺组织细胞的超微结构。采用免疫组织化学法观察白细胞介素-1β(IL-1β)、血红素加氧酶-1(HO-1)、表面活性蛋白A(SP-A)的表达,采用免疫荧光法观察α平滑肌肌动蛋白(α-SMA)的表达。纳米氧化铟锡气管内滴注可导致肺毒性,表现为暴露后3天出现急性炎症,14天出现肉芽肿(结节)形成和胶原增生,56天出现肺泡蛋白沉积症。肺组织病理特征包括典型的肺泡渗出、细胞性纤维结节、肺泡内脂肪滴融合增大、胆固醇结晶肉芽肿和肺泡蛋白沉积症。在暴露84天的大鼠肺组织透射电镜检查中,肺泡内嗜酸性物质(多层、晶格状和髓鞘样结构)显示出异常板层小体(Ⅱ型肺泡上皮细胞特征)以及丰富的粗面内质网和线粒体(成纤维细胞特征)。细胞病理学显示,暴露后28天支气管肺泡灌洗液中出现大量无定形PAS染色阳性物质,肺泡巨噬细胞内可见粉红色颗粒状蛋白样物质。纳米氧化铟锡诱导的大鼠肺损伤有三个特征性发展阶段,即急性炎症、肉芽肿(结节)形成和胶原增生以及肺泡蛋白沉积症,为铟肺疾病的发病机制提供了参考特征模型。

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