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Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion

OBJECTIVE: It has previously been shown that a combination of inhaled nitric oxide (iNO) and intravenous (IV) steroid attenuates endotoxin-induced organ damage in a 6-hour porcine endotoxemia model. We aimed to further explore these effects in a 30-hour model with attention to clinically important v...

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Autores principales: Göranson, Sofie Paues, Goździk, Waldemar, Harbut, Piotr, Ryniak, Stanisław, Zielinski, Stanisław, Haegerstrand, Caroline Gillis, Kübler, Andrzej, Hedenstierna, Göran, Frostell, Claes, Albert, Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020811/
https://www.ncbi.nlm.nih.gov/pubmed/24827456
http://dx.doi.org/10.1371/journal.pone.0096594
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author Göranson, Sofie Paues
Goździk, Waldemar
Harbut, Piotr
Ryniak, Stanisław
Zielinski, Stanisław
Haegerstrand, Caroline Gillis
Kübler, Andrzej
Hedenstierna, Göran
Frostell, Claes
Albert, Johanna
author_facet Göranson, Sofie Paues
Goździk, Waldemar
Harbut, Piotr
Ryniak, Stanisław
Zielinski, Stanisław
Haegerstrand, Caroline Gillis
Kübler, Andrzej
Hedenstierna, Göran
Frostell, Claes
Albert, Johanna
author_sort Göranson, Sofie Paues
collection PubMed
description OBJECTIVE: It has previously been shown that a combination of inhaled nitric oxide (iNO) and intravenous (IV) steroid attenuates endotoxin-induced organ damage in a 6-hour porcine endotoxemia model. We aimed to further explore these effects in a 30-hour model with attention to clinically important variables. DESIGN: Randomized controlled trial. SETTING: University animal laboratory. SUBJECTS: Domestic piglets (n = 30). INTERVENTIONS: Animals were randomized into 5 groups (n = 6 each): 1) Controls, 2) LPS-only (endotoxin/lipopolysaccharide (LPS) infusion), 3) LPS + iNO, 4) LPS + IV steroid, 5) LPS + iNO + IV steroid. MEASUREMENTS AND MAIN RESULTS: Exposure to LPS temporarily increased pulmonary artery mean pressure and impeded renal function with elevated serum creatinine and acidosis compared to a control group over the 30-hour study period. Double treatment with both iNO and IV steroid tended to blunt the deterioration in renal function, although the only significant effect was on Base Excess (p = 0.045). None of the LPS + iNO + IV steroid treated animals died during the study period, whereas one animal died in each of the other LPS-infused groups. CONCLUSIONS: This study suggests that combined early therapy with iNO and IV steroid is associated with partial protection of kidney function after 30 hours of experimental LPS infusion.
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spelling pubmed-40208112014-05-21 Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion Göranson, Sofie Paues Goździk, Waldemar Harbut, Piotr Ryniak, Stanisław Zielinski, Stanisław Haegerstrand, Caroline Gillis Kübler, Andrzej Hedenstierna, Göran Frostell, Claes Albert, Johanna PLoS One Research Article OBJECTIVE: It has previously been shown that a combination of inhaled nitric oxide (iNO) and intravenous (IV) steroid attenuates endotoxin-induced organ damage in a 6-hour porcine endotoxemia model. We aimed to further explore these effects in a 30-hour model with attention to clinically important variables. DESIGN: Randomized controlled trial. SETTING: University animal laboratory. SUBJECTS: Domestic piglets (n = 30). INTERVENTIONS: Animals were randomized into 5 groups (n = 6 each): 1) Controls, 2) LPS-only (endotoxin/lipopolysaccharide (LPS) infusion), 3) LPS + iNO, 4) LPS + IV steroid, 5) LPS + iNO + IV steroid. MEASUREMENTS AND MAIN RESULTS: Exposure to LPS temporarily increased pulmonary artery mean pressure and impeded renal function with elevated serum creatinine and acidosis compared to a control group over the 30-hour study period. Double treatment with both iNO and IV steroid tended to blunt the deterioration in renal function, although the only significant effect was on Base Excess (p = 0.045). None of the LPS + iNO + IV steroid treated animals died during the study period, whereas one animal died in each of the other LPS-infused groups. CONCLUSIONS: This study suggests that combined early therapy with iNO and IV steroid is associated with partial protection of kidney function after 30 hours of experimental LPS infusion. Public Library of Science 2014-05-14 /pmc/articles/PMC4020811/ /pubmed/24827456 http://dx.doi.org/10.1371/journal.pone.0096594 Text en © 2014 Göranson 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Göranson, Sofie Paues
Goździk, Waldemar
Harbut, Piotr
Ryniak, Stanisław
Zielinski, Stanisław
Haegerstrand, Caroline Gillis
Kübler, Andrzej
Hedenstierna, Göran
Frostell, Claes
Albert, Johanna
Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion
title Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion
title_full Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion
title_fullStr Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion
title_full_unstemmed Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion
title_short Organ Dysfunction among Piglets Treated with Inhaled Nitric Oxide and Intravenous Hydrocortisone during Prolonged Endotoxin Infusion
title_sort organ dysfunction among piglets treated with inhaled nitric oxide and intravenous hydrocortisone during prolonged endotoxin infusion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020811/
https://www.ncbi.nlm.nih.gov/pubmed/24827456
http://dx.doi.org/10.1371/journal.pone.0096594
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