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DOI: 10.3791/64097-v
Dingyun Song1,2, Yicong Chen1,3, Xin Wang1,4, Xueying Chen1,2, Shuwei Gao1,3, Wenxiu Xu1,3, Shengnan Yang5, Zai Wang6, Liang Peng7, Huaping Dai1,2
1Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Diseases, Institute of Respiratory Medicine,Chinese Academy of Medical Sciences, 2Graduate School of Peking Union Medical College,Chinese Academy of Medical Science and Peking Union Medical College, 3Capital Medical University, 4Beijing University of Chinese Medicine, 5Tianjin Chest Hospital, 6Institute of Clinical Medical Sciences,China-Japan Friendship Hospital, 7Beijing Key Laboratory for Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Sciences,China-Japan Friendship Hospital
Please note that some of the translations on this page are AI generated. Click here for the English version.
The study introduces a novel model for pulmonary fibrosis using nasal nebulization of bleomycin, allowing for uniform drug distribution in the lungs. This model closely mimics clinical disease characteristics and aids in understanding the pathogenesis of pulmonary fibrosis.
已经使用博来霉素建立了各种肺纤维化动物模型,以阐明肺纤维化的发病机制并寻找新的药物靶点。然而,大多数针对肺组织的肺纤维化模型给药不均匀。在这里,我们提出了一个由鼻腔博来霉素雾化诱导的均匀肺纤维化模型。
在这项研究中,博来霉素的肺间给药是通过鼻雾化进行的,以创建一个与临床疾病特征非常相似的肺纤维化小鼠模型。麻醉后,用食指和拇指按压小鼠的脚趾,确保肢体退缩反射消失。校准仪器后,用柔软的网罩固定麻醉的鼠标。
使用移液管将工作中的 BLM 溶液添加到曝光塔的顶部雾化头中,并运行雾化器 30 分钟以实现稳定的雾化。现在双击 FlexiWare 8 图标。选择 Experimentation Session 并单击 New Study 按钮。
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