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Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0

Maintaining adequate oxygenation during one-lung ventilation (OLV) requires high inspired oxygen fraction (FiO(2)). However, high FiO(2) also causes inflammatory response and lung injury. Therefore, it remains a great interest to clinicians and scientists to optimize the care of patients undergoing...

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Autores principales: Xu, Zeping, Gu, Lianbing, Bian, Qingming, Li, Pengyi, Wang, Lijun, Zhang, Jingyuan, Qian, Yanning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5274513/
https://www.ncbi.nlm.nih.gov/pubmed/28808186
http://dx.doi.org/10.7555/JBR.31.20160108
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author Xu, Zeping
Gu, Lianbing
Bian, Qingming
Li, Pengyi
Wang, Lijun
Zhang, Jingyuan
Qian, Yanning
author_facet Xu, Zeping
Gu, Lianbing
Bian, Qingming
Li, Pengyi
Wang, Lijun
Zhang, Jingyuan
Qian, Yanning
author_sort Xu, Zeping
collection PubMed
description Maintaining adequate oxygenation during one-lung ventilation (OLV) requires high inspired oxygen fraction (FiO(2)). However, high FiO(2) also causes inflammatory response and lung injury. Therefore, it remains a great interest to clinicians and scientists to optimize the care of patients undergoing OLV. The aim of this study was to determine and compare oxygenation, inflammatory response and lung injury during OLV in rabbits using FiO(2) of 0.6 vs. 1.0. After 30 minutes of two-lung ventilation (TLV) as baseline, 30 rabbits were randomly assigned to three groups receiving mechanical ventilation for 3 hours: the sham group, receiving TLV with 0.6 FiO(2); the 1.0 FiO(2) group, receiving OLV with 1.0 FiO(2); the 0.6 FiO(2) group, receiving OLV with 0.6 FiO(2). Pulse oximetry was continuously monitored and arterial blood gas analysis was intermittently conducted. Histopathologic study of lung tissues was performed and inflammatory cytokines and the mRNA and protein of nuclear factor kappa B (NF-κB) p65 were determined. Three of the 10 rabbits in the 0.6 FiO(2) group suffered hypoxemia, defined by pulse oximetric saturation (SpO(2)) less than 90%. Partial pressure of oxygen (PaO(2)), acute lung injury (ALI) score, myeloperoxidase (MPO), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), mRNA and protein of NF-κB p65 were lower in the 0.6 FiO(2) group than in the 1.0 FiO(2) group. In conclusion, during OLV, if FiO(2) of 0.6 can be tolerated, lung injury associated with high FiO(2) can be minimized. Further study is needed to validate this finding in human subjects.
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spelling pubmed-52745132017-04-24 Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0 Xu, Zeping Gu, Lianbing Bian, Qingming Li, Pengyi Wang, Lijun Zhang, Jingyuan Qian, Yanning J Biomed Res Original Article Maintaining adequate oxygenation during one-lung ventilation (OLV) requires high inspired oxygen fraction (FiO(2)). However, high FiO(2) also causes inflammatory response and lung injury. Therefore, it remains a great interest to clinicians and scientists to optimize the care of patients undergoing OLV. The aim of this study was to determine and compare oxygenation, inflammatory response and lung injury during OLV in rabbits using FiO(2) of 0.6 vs. 1.0. After 30 minutes of two-lung ventilation (TLV) as baseline, 30 rabbits were randomly assigned to three groups receiving mechanical ventilation for 3 hours: the sham group, receiving TLV with 0.6 FiO(2); the 1.0 FiO(2) group, receiving OLV with 1.0 FiO(2); the 0.6 FiO(2) group, receiving OLV with 0.6 FiO(2). Pulse oximetry was continuously monitored and arterial blood gas analysis was intermittently conducted. Histopathologic study of lung tissues was performed and inflammatory cytokines and the mRNA and protein of nuclear factor kappa B (NF-κB) p65 were determined. Three of the 10 rabbits in the 0.6 FiO(2) group suffered hypoxemia, defined by pulse oximetric saturation (SpO(2)) less than 90%. Partial pressure of oxygen (PaO(2)), acute lung injury (ALI) score, myeloperoxidase (MPO), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), mRNA and protein of NF-κB p65 were lower in the 0.6 FiO(2) group than in the 1.0 FiO(2) group. In conclusion, during OLV, if FiO(2) of 0.6 can be tolerated, lung injury associated with high FiO(2) can be minimized. Further study is needed to validate this finding in human subjects. Editorial Department of Journal of Biomedical Research 2017-01 2016-09-29 /pmc/articles/PMC5274513/ /pubmed/28808186 http://dx.doi.org/10.7555/JBR.31.20160108 Text en This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Xu, Zeping
Gu, Lianbing
Bian, Qingming
Li, Pengyi
Wang, Lijun
Zhang, Jingyuan
Qian, Yanning
Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0
title Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0
title_full Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0
title_fullStr Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0
title_full_unstemmed Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0
title_short Oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0
title_sort oxygenation, inflammatory response and lung injury during one lung ventilation in rabbits using inspired oxygen fraction of 0.6 vs. 1.0
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5274513/
https://www.ncbi.nlm.nih.gov/pubmed/28808186
http://dx.doi.org/10.7555/JBR.31.20160108
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