Cargando…
Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model
In patients, acute kidney injury (AKI) is often due to haemodynamic impairment associated with hepatic decompensation following extended liver surgery. Mesenchymal stem cells (MSCs) supported tissue protection in a variety of acute and chronic diseases, and might hence ameliorate AKI induced by exte...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454025/ https://www.ncbi.nlm.nih.gov/pubmed/28572613 http://dx.doi.org/10.1038/s41598-017-02670-8 |
_version_ | 1783240762820919296 |
---|---|
author | Tautenhahn, Hans-Michael Brückner, Sandra Uder, Christiane Erler, Silvio Hempel, Madlen von Bergen, Martin Brach, Janine Winkler, Sandra Pankow, Franziska Gittel, Claudia Baunack, Manja Lange, Undine Broschewitz, Johannes Dollinger, Matthias Bartels, Michael Pietsch, Uta Amann, Kerstin Christ, Bruno |
author_facet | Tautenhahn, Hans-Michael Brückner, Sandra Uder, Christiane Erler, Silvio Hempel, Madlen von Bergen, Martin Brach, Janine Winkler, Sandra Pankow, Franziska Gittel, Claudia Baunack, Manja Lange, Undine Broschewitz, Johannes Dollinger, Matthias Bartels, Michael Pietsch, Uta Amann, Kerstin Christ, Bruno |
author_sort | Tautenhahn, Hans-Michael |
collection | PubMed |
description | In patients, acute kidney injury (AKI) is often due to haemodynamic impairment associated with hepatic decompensation following extended liver surgery. Mesenchymal stem cells (MSCs) supported tissue protection in a variety of acute and chronic diseases, and might hence ameliorate AKI induced by extended liver resection. Here, 70% liver resection was performed in male pigs. MSCs were infused through a central venous catheter and haemodynamic parameters as well as markers of acute kidney damage were monitored under intensive care conditions for 24 h post-surgery. Cytokine profiles were established to anticipate the MSCs’ potential mode of action. After extended liver resection, hyperdynamic circulation, associated with hyponatraemia, hyperkalaemia, an increase in serum aldosterone and low urine production developed. These signs of hepatorenal dysfunction and haemodynamic impairment were corrected by MSC treatment. MSCs elevated PDGF levels in the serum, possibly contributing to circulatory homeostasis. Another 14 cytokines were increased in the kidney, most of which are known to support tissue regeneration. In conclusion, MSCs supported kidney and liver function after extended liver resection. They probably acted through paracrine mechanisms improving haemodynamics and tissue homeostasis. They might thus provide a promising strategy to prevent acute kidney injury in the context of post-surgery acute liver failure. |
format | Online Article Text |
id | pubmed-5454025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54540252017-06-06 Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model Tautenhahn, Hans-Michael Brückner, Sandra Uder, Christiane Erler, Silvio Hempel, Madlen von Bergen, Martin Brach, Janine Winkler, Sandra Pankow, Franziska Gittel, Claudia Baunack, Manja Lange, Undine Broschewitz, Johannes Dollinger, Matthias Bartels, Michael Pietsch, Uta Amann, Kerstin Christ, Bruno Sci Rep Article In patients, acute kidney injury (AKI) is often due to haemodynamic impairment associated with hepatic decompensation following extended liver surgery. Mesenchymal stem cells (MSCs) supported tissue protection in a variety of acute and chronic diseases, and might hence ameliorate AKI induced by extended liver resection. Here, 70% liver resection was performed in male pigs. MSCs were infused through a central venous catheter and haemodynamic parameters as well as markers of acute kidney damage were monitored under intensive care conditions for 24 h post-surgery. Cytokine profiles were established to anticipate the MSCs’ potential mode of action. After extended liver resection, hyperdynamic circulation, associated with hyponatraemia, hyperkalaemia, an increase in serum aldosterone and low urine production developed. These signs of hepatorenal dysfunction and haemodynamic impairment were corrected by MSC treatment. MSCs elevated PDGF levels in the serum, possibly contributing to circulatory homeostasis. Another 14 cytokines were increased in the kidney, most of which are known to support tissue regeneration. In conclusion, MSCs supported kidney and liver function after extended liver resection. They probably acted through paracrine mechanisms improving haemodynamics and tissue homeostasis. They might thus provide a promising strategy to prevent acute kidney injury in the context of post-surgery acute liver failure. Nature Publishing Group UK 2017-06-01 /pmc/articles/PMC5454025/ /pubmed/28572613 http://dx.doi.org/10.1038/s41598-017-02670-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tautenhahn, Hans-Michael Brückner, Sandra Uder, Christiane Erler, Silvio Hempel, Madlen von Bergen, Martin Brach, Janine Winkler, Sandra Pankow, Franziska Gittel, Claudia Baunack, Manja Lange, Undine Broschewitz, Johannes Dollinger, Matthias Bartels, Michael Pietsch, Uta Amann, Kerstin Christ, Bruno Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model |
title | Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model |
title_full | Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model |
title_fullStr | Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model |
title_full_unstemmed | Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model |
title_short | Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model |
title_sort | mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454025/ https://www.ncbi.nlm.nih.gov/pubmed/28572613 http://dx.doi.org/10.1038/s41598-017-02670-8 |
work_keys_str_mv | AT tautenhahnhansmichael mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT brucknersandra mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT uderchristiane mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT erlersilvio mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT hempelmadlen mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT vonbergenmartin mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT brachjanine mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT winklersandra mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT pankowfranziska mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT gittelclaudia mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT baunackmanja mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT langeundine mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT broschewitzjohannes mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT dollingermatthias mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT bartelsmichael mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT pietschuta mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT amannkerstin mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel AT christbruno mesenchymalstemcellscorrecthaemodynamicdysfunctionassociatedwithliverinjuryafterextendedresectioninapigmodel |