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Comparison of the effect of lps and pam3 on ventilated lungs
BACKGROUND: While lipopolysaccharide (LPS) from Gram-negative bacteria has been shown to augment inflammation in ventilated lungs information on the effect of Gram-positive bacteria is lacking. Therefore the effect of LPS and a lipopetide from Gram-positive bacteria, PAM3, on ventilated lungs were i...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873469/ https://www.ncbi.nlm.nih.gov/pubmed/20403209 http://dx.doi.org/10.1186/1471-2466-10-20 |
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author | Hauber, Hans P Karp, Dörte Goldmann, Torsten Vollmer, Ekkehard Zabel, Peter |
author_facet | Hauber, Hans P Karp, Dörte Goldmann, Torsten Vollmer, Ekkehard Zabel, Peter |
author_sort | Hauber, Hans P |
collection | PubMed |
description | BACKGROUND: While lipopolysaccharide (LPS) from Gram-negative bacteria has been shown to augment inflammation in ventilated lungs information on the effect of Gram-positive bacteria is lacking. Therefore the effect of LPS and a lipopetide from Gram-positive bacteria, PAM3, on ventilated lungs were investigated. METHODS: C57/Bl6 mice were mechanically ventilated. Sterile saline (sham) and different concentrations of LPS (1 μg and 5 μg) and PAM3 (50 nM and 200 nM) were applied intratracheally. Lung function parameters and expression of MIP-2 and TNFα as well as influx of neutrophils were measured. RESULTS: Mechanical ventilation increased resistance and decreased compliance over time. PAM3 but not LPS significantly increased resistance compared to sham challenge (P < 0.05). Both LPS and PAM3 significantly increased MIP-2 and TNFα mRNA expression compared to sham challenge (P < 0.05). The numbers of neutrophils were significantly increased after LPS at a concentration of 5 μg compared to sham (P < 0.05). PAM3 significantly increased the numbers of neutrophils at both concentrations compared to sham (P < 0.05). CONCLUSIONS: These data suggest that PAM3 similar to LPS enhances ventilator-induced inflammation. Moreover, PAM3 but not LPS increases pulmonary resistance in ventilated lungs. Further studies are warranted to define the role of lipopetides in ventilator-associated lung injury. |
format | Text |
id | pubmed-2873469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28734692010-05-20 Comparison of the effect of lps and pam3 on ventilated lungs Hauber, Hans P Karp, Dörte Goldmann, Torsten Vollmer, Ekkehard Zabel, Peter BMC Pulm Med Research article BACKGROUND: While lipopolysaccharide (LPS) from Gram-negative bacteria has been shown to augment inflammation in ventilated lungs information on the effect of Gram-positive bacteria is lacking. Therefore the effect of LPS and a lipopetide from Gram-positive bacteria, PAM3, on ventilated lungs were investigated. METHODS: C57/Bl6 mice were mechanically ventilated. Sterile saline (sham) and different concentrations of LPS (1 μg and 5 μg) and PAM3 (50 nM and 200 nM) were applied intratracheally. Lung function parameters and expression of MIP-2 and TNFα as well as influx of neutrophils were measured. RESULTS: Mechanical ventilation increased resistance and decreased compliance over time. PAM3 but not LPS significantly increased resistance compared to sham challenge (P < 0.05). Both LPS and PAM3 significantly increased MIP-2 and TNFα mRNA expression compared to sham challenge (P < 0.05). The numbers of neutrophils were significantly increased after LPS at a concentration of 5 μg compared to sham (P < 0.05). PAM3 significantly increased the numbers of neutrophils at both concentrations compared to sham (P < 0.05). CONCLUSIONS: These data suggest that PAM3 similar to LPS enhances ventilator-induced inflammation. Moreover, PAM3 but not LPS increases pulmonary resistance in ventilated lungs. Further studies are warranted to define the role of lipopetides in ventilator-associated lung injury. BioMed Central 2010-04-20 /pmc/articles/PMC2873469/ /pubmed/20403209 http://dx.doi.org/10.1186/1471-2466-10-20 Text en Copyright ©2010 Hauber et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research article Hauber, Hans P Karp, Dörte Goldmann, Torsten Vollmer, Ekkehard Zabel, Peter Comparison of the effect of lps and pam3 on ventilated lungs |
title | Comparison of the effect of lps and pam3 on ventilated lungs |
title_full | Comparison of the effect of lps and pam3 on ventilated lungs |
title_fullStr | Comparison of the effect of lps and pam3 on ventilated lungs |
title_full_unstemmed | Comparison of the effect of lps and pam3 on ventilated lungs |
title_short | Comparison of the effect of lps and pam3 on ventilated lungs |
title_sort | comparison of the effect of lps and pam3 on ventilated lungs |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873469/ https://www.ncbi.nlm.nih.gov/pubmed/20403209 http://dx.doi.org/10.1186/1471-2466-10-20 |
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