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Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat

INTRODUCTION: Successful treatment of severe sepsis and septic shock remains a major challenge in critical care medicine. The recently introduced recombinant human activated protein C (APC) remarkably improved the outcome of septic patients. The influence of APC on intestinal circulation is still po...

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Autores principales: Lehmann, Christian, Meissner, Konrad, Knöck, Andreas, Diedrich, Stephan, Pavlovic, Dragan, Gründling, Matthias, Usichenko, Taras, Wendt, Michael, Birnbaum, Jürgen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794461/
https://www.ncbi.nlm.nih.gov/pubmed/17101035
http://dx.doi.org/10.1186/cc5093
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author Lehmann, Christian
Meissner, Konrad
Knöck, Andreas
Diedrich, Stephan
Pavlovic, Dragan
Gründling, Matthias
Usichenko, Taras
Wendt, Michael
Birnbaum, Jürgen
author_facet Lehmann, Christian
Meissner, Konrad
Knöck, Andreas
Diedrich, Stephan
Pavlovic, Dragan
Gründling, Matthias
Usichenko, Taras
Wendt, Michael
Birnbaum, Jürgen
author_sort Lehmann, Christian
collection PubMed
description INTRODUCTION: Successful treatment of severe sepsis and septic shock remains a major challenge in critical care medicine. The recently introduced recombinant human activated protein C (APC) remarkably improved the outcome of septic patients. The influence of APC on intestinal circulation is still poorly understood. Therefore, the present study aimed to investigate the effects of APC on intestinal microcirculation during experimental endotoxaemia in rats by using intravital microscopy. METHODS: A total of 44 male Lewis rats were randomly assigned to receive intravenous injections of 15 mg/kg lipopolysaccharide alone (LPS) (n = 11) or LPS followed by subsequent injection of 2 mg/kg recombinant human APC (LPS + APC) (n = 11), whereas control animals received either APC (n = 11) or saline (n = 11). Animals underwent observations of functional capillary density and leucocyte adherence on venular endothelium in the microcirculation of the intestinal wall by means of intravital fluorescence microscopy. Indicators of macrocirculation as well as plasma levels of tumour necrosis factor-α, interleukin (IL)-1β, IL-6, and IL-10 were measured. RESULTS: Although APC administration of both LPS-treated and control rats did not change macrocirculation or release of inflammatory cytokines, it increased mucosal and muscular functional capillary density (p < 0.001 and p < 0.05, respectively) and reduced the number of firmly adhering leucocytes in intestinal submucosal V1 and V3 venules (p < 0.01) in LPS + APC-treated compared with LPS-treated animals, which did not receive APC. No remarkable differences that could be attributed to APC treatment were observed between the two control groups. CONCLUSION: APC administration during experimental endotoxaemia improved intestinal microcirculation by protecting functional capillary density as a measure of microvascular perfusion and exerted anti-inflammatory effects by reducing leucocyte adherence to the endothelium in submucosal venules. Therefore, beneficial effects of APC in septic patients might be due, in part, to improved intestinal microcirculation.
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spelling pubmed-17944612007-02-08 Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat Lehmann, Christian Meissner, Konrad Knöck, Andreas Diedrich, Stephan Pavlovic, Dragan Gründling, Matthias Usichenko, Taras Wendt, Michael Birnbaum, Jürgen Crit Care Research INTRODUCTION: Successful treatment of severe sepsis and septic shock remains a major challenge in critical care medicine. The recently introduced recombinant human activated protein C (APC) remarkably improved the outcome of septic patients. The influence of APC on intestinal circulation is still poorly understood. Therefore, the present study aimed to investigate the effects of APC on intestinal microcirculation during experimental endotoxaemia in rats by using intravital microscopy. METHODS: A total of 44 male Lewis rats were randomly assigned to receive intravenous injections of 15 mg/kg lipopolysaccharide alone (LPS) (n = 11) or LPS followed by subsequent injection of 2 mg/kg recombinant human APC (LPS + APC) (n = 11), whereas control animals received either APC (n = 11) or saline (n = 11). Animals underwent observations of functional capillary density and leucocyte adherence on venular endothelium in the microcirculation of the intestinal wall by means of intravital fluorescence microscopy. Indicators of macrocirculation as well as plasma levels of tumour necrosis factor-α, interleukin (IL)-1β, IL-6, and IL-10 were measured. RESULTS: Although APC administration of both LPS-treated and control rats did not change macrocirculation or release of inflammatory cytokines, it increased mucosal and muscular functional capillary density (p < 0.001 and p < 0.05, respectively) and reduced the number of firmly adhering leucocytes in intestinal submucosal V1 and V3 venules (p < 0.01) in LPS + APC-treated compared with LPS-treated animals, which did not receive APC. No remarkable differences that could be attributed to APC treatment were observed between the two control groups. CONCLUSION: APC administration during experimental endotoxaemia improved intestinal microcirculation by protecting functional capillary density as a measure of microvascular perfusion and exerted anti-inflammatory effects by reducing leucocyte adherence to the endothelium in submucosal venules. Therefore, beneficial effects of APC in septic patients might be due, in part, to improved intestinal microcirculation. BioMed Central 2006 2006-11-13 /pmc/articles/PMC1794461/ /pubmed/17101035 http://dx.doi.org/10.1186/cc5093 Text en Copyright © 2006 Lehmann et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lehmann, Christian
Meissner, Konrad
Knöck, Andreas
Diedrich, Stephan
Pavlovic, Dragan
Gründling, Matthias
Usichenko, Taras
Wendt, Michael
Birnbaum, Jürgen
Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat
title Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat
title_full Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat
title_fullStr Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat
title_full_unstemmed Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat
title_short Activated protein C improves intestinal microcirculation in experimental endotoxaemia in the rat
title_sort activated protein c improves intestinal microcirculation in experimental endotoxaemia in the rat
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794461/
https://www.ncbi.nlm.nih.gov/pubmed/17101035
http://dx.doi.org/10.1186/cc5093
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