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Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass
BACKGROUND AND OBJECTIVES: To explore the lung-protective effect of levosimendan (LS) during cardiopulmonary bypass in a canine model by determining the wet/dry weight (W/D) ratio of lung tissue, malonaldehyde (MDA) and superoxide dismutase (SOD) concentrations, and performing a histological evaluat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Cardiology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891605/ https://www.ncbi.nlm.nih.gov/pubmed/27275177 http://dx.doi.org/10.4070/kcj.2016.46.3.402 |
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author | Feng, Junbo Liu, Haiyuan Chen, Jiayi Wang, Jiyuan Liu, Zhuang Ge, Shenglin |
author_facet | Feng, Junbo Liu, Haiyuan Chen, Jiayi Wang, Jiyuan Liu, Zhuang Ge, Shenglin |
author_sort | Feng, Junbo |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: To explore the lung-protective effect of levosimendan (LS) during cardiopulmonary bypass in a canine model by determining the wet/dry weight (W/D) ratio of lung tissue, malonaldehyde (MDA) and superoxide dismutase (SOD) concentrations, and performing a histological evaluation. MATERIALS AND METHODS: Thirty-two canines were divided randomly into four groups and underwent a routine aortic cross-clamping cardiopulmonary bypass procedure for 1 h, followed by recovery for 2 h. Animals were handled as follows: group C (means control group), no special treatment after aortic cross clamping; group P (means pulmonary artery perfusion group), pulmonary artery perfusion with cold oxygenated blood after aortic cross clamping; group LSIV (means intravenous injection of LS group), intravenous injection of LS (65 µg/kg) before thoracotomy, and the rest of the procedure was identical to the control group; group LPS (means pulmonary perfusion with LS group), pulmonary perfusion with cold oxygenated blood combined with LS (65 µg/kg) after aortic cross clamping. Lung tissues were removed and subjected to evaluation of pathological alterations, W/D ratio and MDA and SOD concentrations. RESULTS: In group C, the W/D ratio and MDA concentration were higher, while the SOD concentrations were lower (p<0.05). Compared with groups P and LSIV, the MDA concentration was lower in group LPS, while that of SOD was higher (p<0.05); Light and electron microscopy indicated that LS intervention reduced impairment of lung tissues. CONCLUSION: Our findings suggest that LS plays an important role in protecting lung tissues. |
format | Online Article Text |
id | pubmed-4891605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society of Cardiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-48916052016-06-06 Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass Feng, Junbo Liu, Haiyuan Chen, Jiayi Wang, Jiyuan Liu, Zhuang Ge, Shenglin Korean Circ J Original Article BACKGROUND AND OBJECTIVES: To explore the lung-protective effect of levosimendan (LS) during cardiopulmonary bypass in a canine model by determining the wet/dry weight (W/D) ratio of lung tissue, malonaldehyde (MDA) and superoxide dismutase (SOD) concentrations, and performing a histological evaluation. MATERIALS AND METHODS: Thirty-two canines were divided randomly into four groups and underwent a routine aortic cross-clamping cardiopulmonary bypass procedure for 1 h, followed by recovery for 2 h. Animals were handled as follows: group C (means control group), no special treatment after aortic cross clamping; group P (means pulmonary artery perfusion group), pulmonary artery perfusion with cold oxygenated blood after aortic cross clamping; group LSIV (means intravenous injection of LS group), intravenous injection of LS (65 µg/kg) before thoracotomy, and the rest of the procedure was identical to the control group; group LPS (means pulmonary perfusion with LS group), pulmonary perfusion with cold oxygenated blood combined with LS (65 µg/kg) after aortic cross clamping. Lung tissues were removed and subjected to evaluation of pathological alterations, W/D ratio and MDA and SOD concentrations. RESULTS: In group C, the W/D ratio and MDA concentration were higher, while the SOD concentrations were lower (p<0.05). Compared with groups P and LSIV, the MDA concentration was lower in group LPS, while that of SOD was higher (p<0.05); Light and electron microscopy indicated that LS intervention reduced impairment of lung tissues. CONCLUSION: Our findings suggest that LS plays an important role in protecting lung tissues. The Korean Society of Cardiology 2016-05 2016-05-02 /pmc/articles/PMC4891605/ /pubmed/27275177 http://dx.doi.org/10.4070/kcj.2016.46.3.402 Text en Copyright © 2016 The Korean Society of Cardiology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Feng, Junbo Liu, Haiyuan Chen, Jiayi Wang, Jiyuan Liu, Zhuang Ge, Shenglin Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass |
title | Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass |
title_full | Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass |
title_fullStr | Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass |
title_full_unstemmed | Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass |
title_short | Levosimendan Reduces Lung Injury in a Canine Model of Cardiopulmonary Bypass |
title_sort | levosimendan reduces lung injury in a canine model of cardiopulmonary bypass |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891605/ https://www.ncbi.nlm.nih.gov/pubmed/27275177 http://dx.doi.org/10.4070/kcj.2016.46.3.402 |
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