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The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model

BACKGROUND: Endothelial injury and permeability are a hallmark of sepsis. Initial resuscitation of septic patients with crystalloids is associated with aggravation of endothelial permeability, which may be related either to low protein content or to volume. We investigated whether initial resuscitat...

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Autores principales: van den Brink, Daan P., Kleinveld, Derek J. B., Bongers, Annabel, Vos, Jaël, Roelofs, Joris J. T. H., Weber, Nina C., van Buul, Jaap D., Juffermans, Nicole P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511387/
https://www.ncbi.nlm.nih.gov/pubmed/37728777
http://dx.doi.org/10.1186/s40635-023-00549-9
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author van den Brink, Daan P.
Kleinveld, Derek J. B.
Bongers, Annabel
Vos, Jaël
Roelofs, Joris J. T. H.
Weber, Nina C.
van Buul, Jaap D.
Juffermans, Nicole P.
author_facet van den Brink, Daan P.
Kleinveld, Derek J. B.
Bongers, Annabel
Vos, Jaël
Roelofs, Joris J. T. H.
Weber, Nina C.
van Buul, Jaap D.
Juffermans, Nicole P.
author_sort van den Brink, Daan P.
collection PubMed
description BACKGROUND: Endothelial injury and permeability are a hallmark of sepsis. Initial resuscitation of septic patients with crystalloids is associated with aggravation of endothelial permeability, which may be related either to low protein content or to volume. We investigated whether initial resuscitation with different types of plasma or albumin decreases endothelial dysfunction and organ injury in a pneumosepsis rat model compared to the same volume of crystalloids. STUDY DESIGN AND METHODS: Sprague–Dawley rats were intratracheally inoculated with Streptococcus pneumoniae. Twenty-four hours after inoculation, animals were randomized to 2 control groups and 5 intervention groups (n = 11 per group) to receive resuscitation with a fixed volume (8 mL/kg for 1 h) of either Ringer’s Lactate, 5% human albumin, fresh frozen plasma derived from syngeneic donor rats (rFFP), human-derived plasma (hFFP) or human-derived solvent detergent plasma (SDP). Controls were non-resuscitated (n = 11) and healthy animals. Animals were sacrificed 5 h after start of resuscitation (T = 5). Pulmonary FITC-dextran leakage as a reflection of endothelial permeability was used as the primary outcome. RESULTS: Inoculation with S. Pneumoniae resulted in sepsis, increased median lactate levels (1.6–2.8 mM, p < 0.01), pulmonary FITC-dextran leakage (52–134 µg mL(−1), p < 0.05) and lung injury scores (0.7–6.9, p < 0.001) compared to healthy controls. Compared to animals receiving no resuscitation, animals resuscitated with rFFP had reduced pulmonary FITC leakage (134 vs 58 µg/mL, p = 0.011). However, there were no differences in any other markers of organ or endothelial injury. Resuscitation using different human plasma products or 5% albumin showed no differences in any outcome. CONCLUSIONS: Resuscitation with plasma did not reduce endothelial and organ injury when compared to an equal resuscitation volume of crystalloids. Rat-derived FFP may decrease pulmonary leakage induced by shock. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40635-023-00549-9.
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spelling pubmed-105113872023-09-22 The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model van den Brink, Daan P. Kleinveld, Derek J. B. Bongers, Annabel Vos, Jaël Roelofs, Joris J. T. H. Weber, Nina C. van Buul, Jaap D. Juffermans, Nicole P. Intensive Care Med Exp Research Articles BACKGROUND: Endothelial injury and permeability are a hallmark of sepsis. Initial resuscitation of septic patients with crystalloids is associated with aggravation of endothelial permeability, which may be related either to low protein content or to volume. We investigated whether initial resuscitation with different types of plasma or albumin decreases endothelial dysfunction and organ injury in a pneumosepsis rat model compared to the same volume of crystalloids. STUDY DESIGN AND METHODS: Sprague–Dawley rats were intratracheally inoculated with Streptococcus pneumoniae. Twenty-four hours after inoculation, animals were randomized to 2 control groups and 5 intervention groups (n = 11 per group) to receive resuscitation with a fixed volume (8 mL/kg for 1 h) of either Ringer’s Lactate, 5% human albumin, fresh frozen plasma derived from syngeneic donor rats (rFFP), human-derived plasma (hFFP) or human-derived solvent detergent plasma (SDP). Controls were non-resuscitated (n = 11) and healthy animals. Animals were sacrificed 5 h after start of resuscitation (T = 5). Pulmonary FITC-dextran leakage as a reflection of endothelial permeability was used as the primary outcome. RESULTS: Inoculation with S. Pneumoniae resulted in sepsis, increased median lactate levels (1.6–2.8 mM, p < 0.01), pulmonary FITC-dextran leakage (52–134 µg mL(−1), p < 0.05) and lung injury scores (0.7–6.9, p < 0.001) compared to healthy controls. Compared to animals receiving no resuscitation, animals resuscitated with rFFP had reduced pulmonary FITC leakage (134 vs 58 µg/mL, p = 0.011). However, there were no differences in any other markers of organ or endothelial injury. Resuscitation using different human plasma products or 5% albumin showed no differences in any outcome. CONCLUSIONS: Resuscitation with plasma did not reduce endothelial and organ injury when compared to an equal resuscitation volume of crystalloids. Rat-derived FFP may decrease pulmonary leakage induced by shock. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40635-023-00549-9. Springer International Publishing 2023-09-20 /pmc/articles/PMC10511387/ /pubmed/37728777 http://dx.doi.org/10.1186/s40635-023-00549-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
van den Brink, Daan P.
Kleinveld, Derek J. B.
Bongers, Annabel
Vos, Jaël
Roelofs, Joris J. T. H.
Weber, Nina C.
van Buul, Jaap D.
Juffermans, Nicole P.
The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model
title The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model
title_full The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model
title_fullStr The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model
title_full_unstemmed The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model
title_short The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model
title_sort effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511387/
https://www.ncbi.nlm.nih.gov/pubmed/37728777
http://dx.doi.org/10.1186/s40635-023-00549-9
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