Cargando…

Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats

Preservation or restoration of normal alveolar epithelial barrier function is crucial for pulmonary oedema resolution. Keratinocyte growth factor-2 (KGF-2), a potent epithelial cell mitogen, may have a role in preventing ventilator-induced lung injury (VILI), which occurs frequently in mechanically...

Descripción completa

Detalles Bibliográficos
Autores principales: Bi, Jing, Tong, Lin, Zhu, Xiaodan, Yang, Dong, Bai, Chunxue, Song, Yuanlin, She, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508161/
https://www.ncbi.nlm.nih.gov/pubmed/24650242
http://dx.doi.org/10.1111/jcmm.12269
_version_ 1782381903343517696
author Bi, Jing
Tong, Lin
Zhu, Xiaodan
Yang, Dong
Bai, Chunxue
Song, Yuanlin
She, Jun
author_facet Bi, Jing
Tong, Lin
Zhu, Xiaodan
Yang, Dong
Bai, Chunxue
Song, Yuanlin
She, Jun
author_sort Bi, Jing
collection PubMed
description Preservation or restoration of normal alveolar epithelial barrier function is crucial for pulmonary oedema resolution. Keratinocyte growth factor-2 (KGF-2), a potent epithelial cell mitogen, may have a role in preventing ventilator-induced lung injury (VILI), which occurs frequently in mechanically ventilated patients. The aim of the study was to test the role of KGF-2 in VILI in rats. Forty healthy adult male Sprague-Dawley rats were randomly allocated into four groups, where rats in Groups HVZP (high-volume zero positive end-expiratory pressure) and HVZP+KGF-2 were given intratracheally equal PBS and 5 mg/kg KGF-2 72 hrs before 4 hrs HVZP ventilation (20 ml/kg), respectively, while PBS and KGF-2 were administered in the same manner in Groups Control and KGF-2, which underwent tracheotomy only with spontaneous breathing. Inflammatory cytokines (tumour necrosis factor-α, macrophage inflammatory protein 2), neutrophil and total protein levels in bronchoalveolar lavage fluid and surfactant protein mRNA expression in lung tissue were detected; the number of alveolar type II cells, lung water content and lung morphology were also evaluated. The results indicate that pre-treatment with KGF-2 showed dramatic improvement in lung oedema and inflammation compared with HVZP alone, together with increased surfactant protein mRNA and alveolar type II cells. Our results suggest that KGF-2 might be considered a promising prevention for human VILI or other acute lung injury diseases.
format Online
Article
Text
id pubmed-4508161
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher John Wiley & Sons, Ltd
record_format MEDLINE/PubMed
spelling pubmed-45081612015-07-22 Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats Bi, Jing Tong, Lin Zhu, Xiaodan Yang, Dong Bai, Chunxue Song, Yuanlin She, Jun J Cell Mol Med Original Articles Preservation or restoration of normal alveolar epithelial barrier function is crucial for pulmonary oedema resolution. Keratinocyte growth factor-2 (KGF-2), a potent epithelial cell mitogen, may have a role in preventing ventilator-induced lung injury (VILI), which occurs frequently in mechanically ventilated patients. The aim of the study was to test the role of KGF-2 in VILI in rats. Forty healthy adult male Sprague-Dawley rats were randomly allocated into four groups, where rats in Groups HVZP (high-volume zero positive end-expiratory pressure) and HVZP+KGF-2 were given intratracheally equal PBS and 5 mg/kg KGF-2 72 hrs before 4 hrs HVZP ventilation (20 ml/kg), respectively, while PBS and KGF-2 were administered in the same manner in Groups Control and KGF-2, which underwent tracheotomy only with spontaneous breathing. Inflammatory cytokines (tumour necrosis factor-α, macrophage inflammatory protein 2), neutrophil and total protein levels in bronchoalveolar lavage fluid and surfactant protein mRNA expression in lung tissue were detected; the number of alveolar type II cells, lung water content and lung morphology were also evaluated. The results indicate that pre-treatment with KGF-2 showed dramatic improvement in lung oedema and inflammation compared with HVZP alone, together with increased surfactant protein mRNA and alveolar type II cells. Our results suggest that KGF-2 might be considered a promising prevention for human VILI or other acute lung injury diseases. John Wiley & Sons, Ltd 2014-06 2014-03-21 /pmc/articles/PMC4508161/ /pubmed/24650242 http://dx.doi.org/10.1111/jcmm.12269 Text en © 2014 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Bi, Jing
Tong, Lin
Zhu, Xiaodan
Yang, Dong
Bai, Chunxue
Song, Yuanlin
She, Jun
Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats
title Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats
title_full Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats
title_fullStr Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats
title_full_unstemmed Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats
title_short Keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats
title_sort keratinocyte growth factor-2 intratracheal instillation significantly attenuates ventilator-induced lung injury in rats
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508161/
https://www.ncbi.nlm.nih.gov/pubmed/24650242
http://dx.doi.org/10.1111/jcmm.12269
work_keys_str_mv AT bijing keratinocytegrowthfactor2intratrachealinstillationsignificantlyattenuatesventilatorinducedlunginjuryinrats
AT tonglin keratinocytegrowthfactor2intratrachealinstillationsignificantlyattenuatesventilatorinducedlunginjuryinrats
AT zhuxiaodan keratinocytegrowthfactor2intratrachealinstillationsignificantlyattenuatesventilatorinducedlunginjuryinrats
AT yangdong keratinocytegrowthfactor2intratrachealinstillationsignificantlyattenuatesventilatorinducedlunginjuryinrats
AT baichunxue keratinocytegrowthfactor2intratrachealinstillationsignificantlyattenuatesventilatorinducedlunginjuryinrats
AT songyuanlin keratinocytegrowthfactor2intratrachealinstillationsignificantlyattenuatesventilatorinducedlunginjuryinrats
AT shejun keratinocytegrowthfactor2intratrachealinstillationsignificantlyattenuatesventilatorinducedlunginjuryinrats