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变应性哮喘BALB/c小鼠模型的研究

Study of a BALB/c Mouse Model for Allergic Asthma.

作者信息

Yang Young-Su, Yang Mi-Jin, Cho Kyu-Hyuk, Lee Kyuhong, Kim Yong-Bum, Kim Jin-Sung, Kang Myung-Gyun, Song Chang-Woo, Song Chang-Woo

机构信息

13Division of Inhalation Toxicology, Korea Institute of Toxicology, Korea Research Institute of Chemical Technology, 1051 Shinjeong-dong, Jeongeup, Jeollabuk-do, 580-185 Republic of Korea.

23Division of Toxicological Pathology, Korea institute of Toxicology, Daejeon, 305-343 Korea.

出版信息

Toxicol Res. 2008 Dec;24(4):253-261. doi: 10.5487/TR.2008.24.4.253. Epub 2008 Dec 1.

Abstract

Allergic asthma is a worldwide public health problem and a major socioeconomic burden disease. It is a chronic inflammatory disease marked by airway eosinophilia and goblet cell hyperplasia with mucus hypersecretion. Mouse models have proven as a valuable tool for studying human asthma. In the present report we describe a comparison of mouse asthma models. The experiments were designed as follows: Group I was injected with ovalbumin (OVA, i.p.) on day 1 and challenged with 1% OVA (aerosol exposure) on days 1421. Group II was injected on day 1, 14 and aerosol-immunized on days 1421. Group III was injected on day 1, 14 and immunized by 1% OVA aerosol on days 18~21. We assessed asthma induction by determining the total number of white blood cells (WBC) and eosinophils as well as by measuring cytokine levels in bronchoalveolar lavage fluid (BALF). In addition, we evaluated the histopathological changes of the lungs and determined the concentration of immunoglobulin E (IgE) in serum. Total WBC, eosinophils, Th2 cytokines (IL-4, IL-13) and IgE were significantly increased in group I relative to the other groups. Moreover, histopathological studies show that group I mice show an increase in the infiltration of inflammatory cell-in peribronchial and perivascular areas as well as an overall increase in the number of mucus-containing goblet cells relative to other groups. These data suggest that group I can be a useful model for the study of human asthma pathobiology and the evaluation of existing and novel therapeutic agents.

摘要

过敏性哮喘是一个全球性的公共卫生问题,也是一种主要的社会经济负担疾病。它是一种慢性炎症性疾病,其特征为气道嗜酸性粒细胞增多和杯状细胞增生伴黏液分泌过多。小鼠模型已被证明是研究人类哮喘的宝贵工具。在本报告中,我们描述了小鼠哮喘模型的比较。实验设计如下:第一组在第1天腹腔注射卵清蛋白(OVA),并在第14至21天用1% OVA(雾化暴露)进行激发。第二组在第1天、第14天注射,并在第14至21天进行雾化免疫。第三组在第1天、第14天注射,并在第18至21天用1% OVA气雾剂进行免疫。我们通过测定白细胞(WBC)和嗜酸性粒细胞的总数以及测量支气管肺泡灌洗液(BALF)中的细胞因子水平来评估哮喘的诱导情况。此外,我们评估了肺部的组织病理学变化,并测定了血清中免疫球蛋白E(IgE)的浓度。相对于其他组,第一组的总WBC、嗜酸性粒细胞、Th2细胞因子(IL-4、IL-13)和IgE显著增加。此外,组织病理学研究表明,相对于其他组,第一组小鼠在支气管周围和血管周围区域的炎症细胞浸润增加,以及含黏液的杯状细胞数量总体增加。这些数据表明,第一组可作为研究人类哮喘病理生物学以及评估现有和新型治疗药物的有用模型。

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Study of a BALB/c Mouse Model for Allergic Asthma.变应性哮喘BALB/c小鼠模型的研究
Toxicol Res. 2008 Dec;24(4):253-261. doi: 10.5487/TR.2008.24.4.253. Epub 2008 Dec 1.

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