首页> 外文期刊>The Journal of toxicological sciences >Perinatal exposure to tetrabromobisphenol A (TBBPA), a brominated flame retardant, exacerbated the pneumonia in respiratory syncytial virus (RSV)-infected offspring mice
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Perinatal exposure to tetrabromobisphenol A (TBBPA), a brominated flame retardant, exacerbated the pneumonia in respiratory syncytial virus (RSV)-infected offspring mice

机译:围产期暴露于四溴双酚A(TBBPA),溴化阻燃剂,加剧了呼吸道合胞病毒(RSV)的肺炎(RSV)的后代小鼠

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摘要

To investigate the effects of perinatal exposure to tetrabromobisphenol A (TBBPA), a brominated flame retardant, on the immune system, a respiratory syncytial virus (RSV) infection mouse model was utilized. Female mice were exposed to TBBPA mixed with the diet from 10 days after conception to weaning on postnatal day 21. Offspring mice were infected intranasally with A2 strain of RSV. Although no general toxicological sign was observed, the pulmonary viral titers of offspring mice exposed to 0.1% TBBPA were significantly increased compared with the control on day 5 post-infection. TBBPA did not affect RSV growth in vitro. Histopathological analysis confirmed that the exacerbation of interstitial pneumonia was due to TBBPA-exposure in the lung tissues in RSV-infected offspring. Moreover, gene expression of interleukin (IL)-24 was shown to be elevated typically in the lung tissues of TBB-PA-treated offspring by a DNA microarray and was also confirmed by immunohistopathological analysis using an anti-IL-24 antibody. Thus, developmental exposure to TBBPA affected the immune response to RSV infection, resulting in the exacerbation of pneumonia. Thus, IL-24 should be a key molecule to understand the mechanism of action of TBBPA.
机译:为了探讨围产产暴露于四溴二苯酚A(TBBPA)的影响,使用溴化阻燃剂对免疫系统,使用呼吸道合胞病毒(RSV)感染小鼠模型。在第21天发生概念后10天将雌性小鼠暴露于与饮食混合的TBBPA混合在10天后。后代小鼠用A2株的RSV感染鼻内感染。虽然没有观察到一般的毒理学标志,但与感染后第5天的对照相比,暴露于0.1%TBBPA的后代小鼠的后代小鼠的肺病滴度显着增加。 TBBPA在体外没有影响RSV生长。组织病理学分析证实,间质肺炎的加剧是由于RSV感染后代的肺组织中的TBBPA暴露。此外,显示白细胞介素(IL)-24的基因表达通常在DNA微阵列的TBB-PA处理后代的肺组织中升高,并且还通过使用抗IL-24抗体来证实免疫病理学分析。因此,对TBBPA的发育暴露影响了对RSV感染的免疫应答,导致肺炎的加剧。因此,IL-24应该是理解TBBPA作用机制的关键分子。

著录项

  • 来源
  • 作者单位

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Microbiol 1714-1 Yoshino Nobeoka Miyazaki;

    Natl Inst Hlth Sci Div Risk Assessment Biol Safety Res Ctr Setagaya Ku 1-18-1 Kamiyoga Tokyo;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Biochem 1714-1 Yoshino Nobeoka Miyazaki;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Microbiol 1714-1 Yoshino Nobeoka Miyazaki;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Microbiol 1714-1 Yoshino Nobeoka Miyazaki;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Biochem 1714-1 Yoshino Nobeoka Miyazaki;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Microbiol 1714-1 Yoshino Nobeoka Miyazaki;

    Kyushu Univ Hlth &

    Welf Sch Pharmaceut Sci Dept Microbiol &

    Infect Dis 1714-1 Yoshino Nobeoka;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Biochem 1714-1 Yoshino Nobeoka Miyazaki;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Biochem 1714-1 Yoshino Nobeoka Miyazaki;

    Kyushu Univ Hlth &

    Welf Grad Sch Clin Pharm Dept Biochem 1714-1 Yoshino Nobeoka Miyazaki;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

    TBBPA; RSV; Pneumonia; IL-24;

    机译:TBBPA;RSV;肺炎;IL-24;
  • 入库时间 2022-08-20 07:21:22

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