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Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury
OBJECTIVES: Antiorthostatic suspension (AOS) is ground-based model of simulated microgravity. There is still no study about the effect of long-term microgravity on the clinical course of acute lung injury. We evaluated the effect of simulated microgravity using AOS in a murine model of acute lung in...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society of Otorhinolaryngology-Head and Neck Surgery
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115144/ https://www.ncbi.nlm.nih.gov/pubmed/27334509 http://dx.doi.org/10.21053/ceo.2015.01599 |
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author | Jang, Tae Young Jung, Ah-Yeoun Kim, Young Hyo |
author_facet | Jang, Tae Young Jung, Ah-Yeoun Kim, Young Hyo |
author_sort | Jang, Tae Young |
collection | PubMed |
description | OBJECTIVES: Antiorthostatic suspension (AOS) is ground-based model of simulated microgravity. There is still no study about the effect of long-term microgravity on the clinical course of acute lung injury. We evaluated the effect of simulated microgravity using AOS in a murine model of acute lung injury by lipopolysaccharide (LPS). METHODS: Thirty BALB/c mice were used. During 4 weeks, mice were equally allocated to control (free movement), restraint (tail suspended, but hindlimbs not unloaded), and AOS group (hindlimb unloaded). After then, mice got intranasal challenge with LPS (20 mg/kg, 50 μL). We measured: weight gain before and after AOS, the number of inflammatory cells and titers of cytokines (interleukin [IL]-1β, IL-6, IL-10, tumor necrosis factor-α, and interferon-γ) in bronchoalveolar lavage (BAL) fluid, titer of myeloperoxidase (MPO) in serum and lung homogenate, and histopathologic examination of lung tissue. RESULTS: AOS group had significant weight loss compared to control and restraint group (P<0.001). AOS group also showed significantly decreased lymphocytes (P=0.023) compared to control group. In AOS group, titer for IL-1β in BAL fluid was significantly lower than restraint group (P=0.049). Titer for serum MPO was significantly decreased in AOS group compared to restraint group (P=0.004). However, there was no significant difference of MPO titers in lung tissue between groups. Histopathologic examination of lung tissue revealed no significant difference in the degree of pulmonary infiltration between restraint and AOS group. CONCLUSION: In spite of modest anti-inflammatory effect, prolonged AOS caused no significant change in LPS-induced pulmonary inflammation. |
format | Online Article Text |
id | pubmed-5115144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society of Otorhinolaryngology-Head and Neck Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-51151442016-12-01 Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury Jang, Tae Young Jung, Ah-Yeoun Kim, Young Hyo Clin Exp Otorhinolaryngol Original Article OBJECTIVES: Antiorthostatic suspension (AOS) is ground-based model of simulated microgravity. There is still no study about the effect of long-term microgravity on the clinical course of acute lung injury. We evaluated the effect of simulated microgravity using AOS in a murine model of acute lung injury by lipopolysaccharide (LPS). METHODS: Thirty BALB/c mice were used. During 4 weeks, mice were equally allocated to control (free movement), restraint (tail suspended, but hindlimbs not unloaded), and AOS group (hindlimb unloaded). After then, mice got intranasal challenge with LPS (20 mg/kg, 50 μL). We measured: weight gain before and after AOS, the number of inflammatory cells and titers of cytokines (interleukin [IL]-1β, IL-6, IL-10, tumor necrosis factor-α, and interferon-γ) in bronchoalveolar lavage (BAL) fluid, titer of myeloperoxidase (MPO) in serum and lung homogenate, and histopathologic examination of lung tissue. RESULTS: AOS group had significant weight loss compared to control and restraint group (P<0.001). AOS group also showed significantly decreased lymphocytes (P=0.023) compared to control group. In AOS group, titer for IL-1β in BAL fluid was significantly lower than restraint group (P=0.049). Titer for serum MPO was significantly decreased in AOS group compared to restraint group (P=0.004). However, there was no significant difference of MPO titers in lung tissue between groups. Histopathologic examination of lung tissue revealed no significant difference in the degree of pulmonary infiltration between restraint and AOS group. CONCLUSION: In spite of modest anti-inflammatory effect, prolonged AOS caused no significant change in LPS-induced pulmonary inflammation. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2016-12 2016-06-18 /pmc/articles/PMC5115144/ /pubmed/27334509 http://dx.doi.org/10.21053/ceo.2015.01599 Text en Copyright © 2016 by Korean Society of Otorhinolaryngology-Head and Neck Surgery This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jang, Tae Young Jung, Ah-Yeoun Kim, Young Hyo Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury |
title | Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury |
title_full | Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury |
title_fullStr | Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury |
title_full_unstemmed | Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury |
title_short | Effect of Long-Term Antiorthostatic Suspension in a Murine Model of Acute Lung Injury |
title_sort | effect of long-term antiorthostatic suspension in a murine model of acute lung injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115144/ https://www.ncbi.nlm.nih.gov/pubmed/27334509 http://dx.doi.org/10.21053/ceo.2015.01599 |
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