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Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes

OBJECTIVE: Asphyxia of newborns is a severe and frequent challenge of the peri- and postnatal period. The purpose of this study was to study early morphological, immunological and structural alterations in lung tissue after asphyxia and hemorrhage (AH). METHODS: 44 neonatal piglets (age 32 hrs) unde...

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Autores principales: Weber, Birte, Mendler, Marc Robin, Lackner, Ina, von Zelewski, Alexander, Höfler, Severin, Baur, Meike, Braun, Christian Karl, Hummler, Helmut, Schwarz, Stephan, Pressmar, Jochen, Kalbitz, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611609/
https://www.ncbi.nlm.nih.gov/pubmed/31276543
http://dx.doi.org/10.1371/journal.pone.0219211
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author Weber, Birte
Mendler, Marc Robin
Lackner, Ina
von Zelewski, Alexander
Höfler, Severin
Baur, Meike
Braun, Christian Karl
Hummler, Helmut
Schwarz, Stephan
Pressmar, Jochen
Kalbitz, Miriam
author_facet Weber, Birte
Mendler, Marc Robin
Lackner, Ina
von Zelewski, Alexander
Höfler, Severin
Baur, Meike
Braun, Christian Karl
Hummler, Helmut
Schwarz, Stephan
Pressmar, Jochen
Kalbitz, Miriam
author_sort Weber, Birte
collection PubMed
description OBJECTIVE: Asphyxia of newborns is a severe and frequent challenge of the peri- and postnatal period. The purpose of this study was to study early morphological, immunological and structural alterations in lung tissue after asphyxia and hemorrhage (AH). METHODS: 44 neonatal piglets (age 32 hrs) underwent asphyxia and hemorrhage (AH) and were treated according to the international liaison committee of resuscitation (ILCOR) guidelines. For this study, 15 piglets (blood transfusion (RBC) n = 9; NaCl n = 6, mean age 31 hrs) were randomly picked. 4 hours after ROSC (return of spontaneous circulation), lung tissue and blood samples were collected. RESULTS: An elevation of myeloperoxidase (MPO) activity was observed 4 hrs after AH accompanied by an increase of surfactant D after RBC treatment. After AH tight junction proteins Claudin 18 and junctional adhesion molecule 1 (JAM1) were down-regulated, whereas Occludin was increased. Furthermore, after AH and RBC treatment dephosphorylated active form of Connexin 43 was increased. CONCLUSIONS: AH in neonatal pigs is associated with early lung injury, inflammation and alterations of tight junctions (Claudin, Occludin, JAM-1) and gap junctions (Connexin 43) in lung tissue, which contributes to the development of lung edema and impaired function.
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spelling pubmed-66116092019-07-12 Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes Weber, Birte Mendler, Marc Robin Lackner, Ina von Zelewski, Alexander Höfler, Severin Baur, Meike Braun, Christian Karl Hummler, Helmut Schwarz, Stephan Pressmar, Jochen Kalbitz, Miriam PLoS One Research Article OBJECTIVE: Asphyxia of newborns is a severe and frequent challenge of the peri- and postnatal period. The purpose of this study was to study early morphological, immunological and structural alterations in lung tissue after asphyxia and hemorrhage (AH). METHODS: 44 neonatal piglets (age 32 hrs) underwent asphyxia and hemorrhage (AH) and were treated according to the international liaison committee of resuscitation (ILCOR) guidelines. For this study, 15 piglets (blood transfusion (RBC) n = 9; NaCl n = 6, mean age 31 hrs) were randomly picked. 4 hours after ROSC (return of spontaneous circulation), lung tissue and blood samples were collected. RESULTS: An elevation of myeloperoxidase (MPO) activity was observed 4 hrs after AH accompanied by an increase of surfactant D after RBC treatment. After AH tight junction proteins Claudin 18 and junctional adhesion molecule 1 (JAM1) were down-regulated, whereas Occludin was increased. Furthermore, after AH and RBC treatment dephosphorylated active form of Connexin 43 was increased. CONCLUSIONS: AH in neonatal pigs is associated with early lung injury, inflammation and alterations of tight junctions (Claudin, Occludin, JAM-1) and gap junctions (Connexin 43) in lung tissue, which contributes to the development of lung edema and impaired function. Public Library of Science 2019-07-05 /pmc/articles/PMC6611609/ /pubmed/31276543 http://dx.doi.org/10.1371/journal.pone.0219211 Text en © 2019 Weber et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Weber, Birte
Mendler, Marc Robin
Lackner, Ina
von Zelewski, Alexander
Höfler, Severin
Baur, Meike
Braun, Christian Karl
Hummler, Helmut
Schwarz, Stephan
Pressmar, Jochen
Kalbitz, Miriam
Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes
title Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes
title_full Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes
title_fullStr Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes
title_full_unstemmed Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes
title_short Lung injury after asphyxia and hemorrhagic shock in newborn piglets: Analysis of structural and inflammatory changes
title_sort lung injury after asphyxia and hemorrhagic shock in newborn piglets: analysis of structural and inflammatory changes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611609/
https://www.ncbi.nlm.nih.gov/pubmed/31276543
http://dx.doi.org/10.1371/journal.pone.0219211
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