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Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model

BACKGROUND: Blood purification is an emerging approach to dampening the cytokine storm. This study aims to assess the efficacy of HA330 resin-directed hemoadsorption (HA) on endotoxin-induced porcine acute respiratory distress syndrome (ARDS) model. METHODS: Twenty-four Chinese domestic pigs were al...

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Autores principales: Xu, Xuefeng, Jia, Chune, Luo, Sa, Li, Yanming, Xiao, Fei, Dai, Huaping, Wang, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555961/
https://www.ncbi.nlm.nih.gov/pubmed/28808944
http://dx.doi.org/10.1186/s13613-017-0287-0
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author Xu, Xuefeng
Jia, Chune
Luo, Sa
Li, Yanming
Xiao, Fei
Dai, Huaping
Wang, Chen
author_facet Xu, Xuefeng
Jia, Chune
Luo, Sa
Li, Yanming
Xiao, Fei
Dai, Huaping
Wang, Chen
author_sort Xu, Xuefeng
collection PubMed
description BACKGROUND: Blood purification is an emerging approach to dampening the cytokine storm. This study aims to assess the efficacy of HA330 resin-directed hemoadsorption (HA) on endotoxin-induced porcine acute respiratory distress syndrome (ARDS) model. METHODS: Twenty-four Chinese domestic pigs were allocated into saline group receiving intravenous infusion of saline (N = 6) and endotoxin group receiving intravenous infusion of LPS (N = 18). When ALI model was initially diagnosed, six pigs in the LPS and saline group were killed for BALF and histopathological analysis. The remaining 12 pigs in LPS group received 3-h HA (N = 6) or HA-sham (N = 6) treatment, respectively. Following another 5-h observation, animals were killed. Variables on hemodynamics, blood gases and lung mechanics were recorded at a series of time points. Differentially expressed cytokines and proteins were determined by ELISA and proteomics. RESULTS: HA treatment significantly improved injured oxygenation induced by LPS. HA also partially improved the barrier permeability and reduced lung edema and inflammation/injury induced by LPS infusion. Proteomic analysis showed the differentially expressed proteins between HA- and HA-sham-treated groups mostly belonged to the categories of acute inflammation/immune response, and proteolysis. CONCLUSIONS: Hemoadsorption improved ARDS possibly by blunting the cytokine storm and by restoring homeostasis of the disordered proteome milieu in the exudative phase. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-017-0287-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-55559612017-08-29 Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model Xu, Xuefeng Jia, Chune Luo, Sa Li, Yanming Xiao, Fei Dai, Huaping Wang, Chen Ann Intensive Care Research BACKGROUND: Blood purification is an emerging approach to dampening the cytokine storm. This study aims to assess the efficacy of HA330 resin-directed hemoadsorption (HA) on endotoxin-induced porcine acute respiratory distress syndrome (ARDS) model. METHODS: Twenty-four Chinese domestic pigs were allocated into saline group receiving intravenous infusion of saline (N = 6) and endotoxin group receiving intravenous infusion of LPS (N = 18). When ALI model was initially diagnosed, six pigs in the LPS and saline group were killed for BALF and histopathological analysis. The remaining 12 pigs in LPS group received 3-h HA (N = 6) or HA-sham (N = 6) treatment, respectively. Following another 5-h observation, animals were killed. Variables on hemodynamics, blood gases and lung mechanics were recorded at a series of time points. Differentially expressed cytokines and proteins were determined by ELISA and proteomics. RESULTS: HA treatment significantly improved injured oxygenation induced by LPS. HA also partially improved the barrier permeability and reduced lung edema and inflammation/injury induced by LPS infusion. Proteomic analysis showed the differentially expressed proteins between HA- and HA-sham-treated groups mostly belonged to the categories of acute inflammation/immune response, and proteolysis. CONCLUSIONS: Hemoadsorption improved ARDS possibly by blunting the cytokine storm and by restoring homeostasis of the disordered proteome milieu in the exudative phase. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-017-0287-0) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-08-14 /pmc/articles/PMC5555961/ /pubmed/28808944 http://dx.doi.org/10.1186/s13613-017-0287-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Xu, Xuefeng
Jia, Chune
Luo, Sa
Li, Yanming
Xiao, Fei
Dai, Huaping
Wang, Chen
Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model
title Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model
title_full Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model
title_fullStr Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model
title_full_unstemmed Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model
title_short Effect of HA330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model
title_sort effect of ha330 resin-directed hemoadsorption on a porcine acute respiratory distress syndrome model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555961/
https://www.ncbi.nlm.nih.gov/pubmed/28808944
http://dx.doi.org/10.1186/s13613-017-0287-0
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