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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.
폐섬유증의 발병기전을 규명하고 새로운 약물 표적을 찾기 위해 블레오마이신을 이용한 다양한 폐섬유증 동물모델을 확립하였습니다. 그러나 폐 조직을 표적으로 하는 대부분의 폐섬유증 모델은 약물 투여가 고르지 않습니다. 여기에서는 비강 표백균 분무에 의해 유도되는 균일한 폐섬유증 모델을 제안합니다.
이 연구에서는 Bleomycin의 폐 간 투여를 비강 분무에 의해 수행하여 임상 질병 특성을 밀접하게 모방한 폐 섬유증의 마우스 모델을 만듭니다. 마취 후 쥐의 발가락을 검지와 엄지로 눌러 사지 후퇴 반사가 사라졌는지 확인합니다. 기기가 보정되면 부드러운 메쉬 커버로 마취된 마우스를 고정합니다.
피펫을 사용하여 작동하는 BLM 용액을 노광탑의 상단 분무 헤드에 추가하고 분무기를 30분 동안 작동시켜 안정적인 분무를 달성합니다. 이제 FlexiWare 8 아이콘을 두 번 클릭합니다. 실험 세션을 선택하고 새 연구 버튼을 클릭합니다.
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