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A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model

BACKGROUND: Recurrent lower respiratory tract infection or chronic pulmonary infection often occur in children with chronic lung diseases (CLDs). By continuous lung inflammation, recurrent and chronic infection could cause irreversible airway structural and lung function damage, which eventually lea...

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Autores principales: Mai, Kailin, Chen, Xiaowen, Zhang, Kangkang, Gu, Shujun, Wu, Xiao, Gu, Zihao, Wu, Zhongji, Huang, Kaiyin, Liu, Zhenwei, Yang, Zifeng, Chen, Dehui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442212/
https://www.ncbi.nlm.nih.gov/pubmed/36072534
http://dx.doi.org/10.21037/tp-22-44
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author Mai, Kailin
Chen, Xiaowen
Zhang, Kangkang
Gu, Shujun
Wu, Xiao
Gu, Zihao
Wu, Zhongji
Huang, Kaiyin
Liu, Zhenwei
Yang, Zifeng
Chen, Dehui
author_facet Mai, Kailin
Chen, Xiaowen
Zhang, Kangkang
Gu, Shujun
Wu, Xiao
Gu, Zihao
Wu, Zhongji
Huang, Kaiyin
Liu, Zhenwei
Yang, Zifeng
Chen, Dehui
author_sort Mai, Kailin
collection PubMed
description BACKGROUND: Recurrent lower respiratory tract infection or chronic pulmonary infection often occur in children with chronic lung diseases (CLDs). By continuous lung inflammation, recurrent and chronic infection could cause irreversible airway structural and lung function damage, which eventually leads to respiratory failure and death. METHODS: In purpose of recapitulating persistent high-intensity lung inflammation caused by recurrent lower respiratory tract infection or chronic infection, we established a juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillations of lipopolysaccharides (LPS) from Pseudomonas aeruginosa once a week for 4 weeks. Four-week-old C57BL/6N mice were divided into 4 groups, including LPS(0.5) group (n=15), LPS(1.0) group (n=15), Control group (n=15) and Normal group (n=15). Mice in LPS(0.5) group and LPS(1.0) group were instilled intratracheally with 0.5 mg/kg LPS and 1.0 mg/kg LPS respectively. Mice in control group were instilled intratracheally with LPS-free sterile 0.9% NaCl, whereas normal group received no treatment. The successful chronic lung inflammation murine model was validated via (I) pathological manifestations of chronic inflammatory mononuclear-cell infiltration and lung parenchyma damage; (II) decreased lung function. RESULTS: All mice in LPS(1.0) group died before the third instillation. No death after instillation was observed in Control and LPS(0.5) group. Histological analysis revealed that in LPS(0.5) group, 7 days after the third instillation, most bronchus and parabronchial vessels were wrapped by infiltrating monocytes and lymphocyte and alveolar cavities were compressed, which were not observed in control and normal group. Also, ratio of forced expiratory volume in 0.1 second (FEV(0.1)) and forced vital capacity (FVC) in LPS(0.5) group was significantly lower (P<0.0001) than both control group and normal group, suggesting ventilatory dysfunction developed after repeatedly intratracheal instillation once a week for 4 weeks. CONCLUSIONS: Intratracheal instillation of 0.5 mg/kg LPS once a week for 4 weeks can cause chronic lung inflammation in young mice.
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spelling pubmed-94422122022-09-06 A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model Mai, Kailin Chen, Xiaowen Zhang, Kangkang Gu, Shujun Wu, Xiao Gu, Zihao Wu, Zhongji Huang, Kaiyin Liu, Zhenwei Yang, Zifeng Chen, Dehui Transl Pediatr Original Article BACKGROUND: Recurrent lower respiratory tract infection or chronic pulmonary infection often occur in children with chronic lung diseases (CLDs). By continuous lung inflammation, recurrent and chronic infection could cause irreversible airway structural and lung function damage, which eventually leads to respiratory failure and death. METHODS: In purpose of recapitulating persistent high-intensity lung inflammation caused by recurrent lower respiratory tract infection or chronic infection, we established a juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillations of lipopolysaccharides (LPS) from Pseudomonas aeruginosa once a week for 4 weeks. Four-week-old C57BL/6N mice were divided into 4 groups, including LPS(0.5) group (n=15), LPS(1.0) group (n=15), Control group (n=15) and Normal group (n=15). Mice in LPS(0.5) group and LPS(1.0) group were instilled intratracheally with 0.5 mg/kg LPS and 1.0 mg/kg LPS respectively. Mice in control group were instilled intratracheally with LPS-free sterile 0.9% NaCl, whereas normal group received no treatment. The successful chronic lung inflammation murine model was validated via (I) pathological manifestations of chronic inflammatory mononuclear-cell infiltration and lung parenchyma damage; (II) decreased lung function. RESULTS: All mice in LPS(1.0) group died before the third instillation. No death after instillation was observed in Control and LPS(0.5) group. Histological analysis revealed that in LPS(0.5) group, 7 days after the third instillation, most bronchus and parabronchial vessels were wrapped by infiltrating monocytes and lymphocyte and alveolar cavities were compressed, which were not observed in control and normal group. Also, ratio of forced expiratory volume in 0.1 second (FEV(0.1)) and forced vital capacity (FVC) in LPS(0.5) group was significantly lower (P<0.0001) than both control group and normal group, suggesting ventilatory dysfunction developed after repeatedly intratracheal instillation once a week for 4 weeks. CONCLUSIONS: Intratracheal instillation of 0.5 mg/kg LPS once a week for 4 weeks can cause chronic lung inflammation in young mice. AME Publishing Company 2022-08 /pmc/articles/PMC9442212/ /pubmed/36072534 http://dx.doi.org/10.21037/tp-22-44 Text en 2022 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Mai, Kailin
Chen, Xiaowen
Zhang, Kangkang
Gu, Shujun
Wu, Xiao
Gu, Zihao
Wu, Zhongji
Huang, Kaiyin
Liu, Zhenwei
Yang, Zifeng
Chen, Dehui
A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model
title A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model
title_full A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model
title_fullStr A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model
title_full_unstemmed A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model
title_short A juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model
title_sort juvenile murine model with chronic lung inflammation induced by repeated intratracheal instillation of lipopolysaccharides: a versatile and replicable model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442212/
https://www.ncbi.nlm.nih.gov/pubmed/36072534
http://dx.doi.org/10.21037/tp-22-44
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