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O-GlcNAc stimulation: A new metabolic approach to treat septic shock

Septic shock is a systemic inflammation associated with cell metabolism disorders and cardiovascular dysfunction. Increases in O-GlcNAcylation have shown beneficial cardiovascular effects in acute pathologies. We used two different rat models to evaluate the beneficial effects of O-GlcNAc stimulatio...

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Autores principales: Ferron, Marine, Cadiet, Julien, Persello, Antoine, Prat, Valentine, Denis, Manon, Erraud, Angélique, Aillerie, Virginie, Mevel, Mathieu, Bigot, Edith, Chatham, John C., Gauthier, Chantal, Rozec, Bertrand, Lauzier, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904741/
https://www.ncbi.nlm.nih.gov/pubmed/31822776
http://dx.doi.org/10.1038/s41598-019-55381-7
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author Ferron, Marine
Cadiet, Julien
Persello, Antoine
Prat, Valentine
Denis, Manon
Erraud, Angélique
Aillerie, Virginie
Mevel, Mathieu
Bigot, Edith
Chatham, John C.
Gauthier, Chantal
Rozec, Bertrand
Lauzier, Benjamin
author_facet Ferron, Marine
Cadiet, Julien
Persello, Antoine
Prat, Valentine
Denis, Manon
Erraud, Angélique
Aillerie, Virginie
Mevel, Mathieu
Bigot, Edith
Chatham, John C.
Gauthier, Chantal
Rozec, Bertrand
Lauzier, Benjamin
author_sort Ferron, Marine
collection PubMed
description Septic shock is a systemic inflammation associated with cell metabolism disorders and cardiovascular dysfunction. Increases in O-GlcNAcylation have shown beneficial cardiovascular effects in acute pathologies. We used two different rat models to evaluate the beneficial effects of O-GlcNAc stimulation at the early phase of septic shock. Rats received lipopolysaccharide (LPS) to induce endotoxemic shock or saline (control) and fluid resuscitation (R) with or without O-GlcNAc stimulation (NButGT–10 mg/kg) 1 hour after shock induction. For the second model, rats received cecal ligature and puncture (CLP) surgery and fluid therapy with or without NButGT. Cardiovascular function was evaluated and heart and blood samples were collected and analysed. NButGT treatment efficiently increased total O-GlcNAc without modification of HBP enzyme expression.Treatment improved circulating parameters and cardiovascular function in both models, and restored SERCA2a expression levels. NButGT treatment also reduced animal mortality. In this study, we demonstrate that in septic shock O-GlcNAc stimulation improves global animal and cardiovascular function outcomes associated with a restoration of SERCA2a levels. This pre-clinical study opens avenues for a potential therapy of early-stage septic shock.
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spelling pubmed-69047412019-12-13 O-GlcNAc stimulation: A new metabolic approach to treat septic shock Ferron, Marine Cadiet, Julien Persello, Antoine Prat, Valentine Denis, Manon Erraud, Angélique Aillerie, Virginie Mevel, Mathieu Bigot, Edith Chatham, John C. Gauthier, Chantal Rozec, Bertrand Lauzier, Benjamin Sci Rep Article Septic shock is a systemic inflammation associated with cell metabolism disorders and cardiovascular dysfunction. Increases in O-GlcNAcylation have shown beneficial cardiovascular effects in acute pathologies. We used two different rat models to evaluate the beneficial effects of O-GlcNAc stimulation at the early phase of septic shock. Rats received lipopolysaccharide (LPS) to induce endotoxemic shock or saline (control) and fluid resuscitation (R) with or without O-GlcNAc stimulation (NButGT–10 mg/kg) 1 hour after shock induction. For the second model, rats received cecal ligature and puncture (CLP) surgery and fluid therapy with or without NButGT. Cardiovascular function was evaluated and heart and blood samples were collected and analysed. NButGT treatment efficiently increased total O-GlcNAc without modification of HBP enzyme expression.Treatment improved circulating parameters and cardiovascular function in both models, and restored SERCA2a expression levels. NButGT treatment also reduced animal mortality. In this study, we demonstrate that in septic shock O-GlcNAc stimulation improves global animal and cardiovascular function outcomes associated with a restoration of SERCA2a levels. This pre-clinical study opens avenues for a potential therapy of early-stage septic shock. Nature Publishing Group UK 2019-12-10 /pmc/articles/PMC6904741/ /pubmed/31822776 http://dx.doi.org/10.1038/s41598-019-55381-7 Text en © The Author(s) 2019 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
Ferron, Marine
Cadiet, Julien
Persello, Antoine
Prat, Valentine
Denis, Manon
Erraud, Angélique
Aillerie, Virginie
Mevel, Mathieu
Bigot, Edith
Chatham, John C.
Gauthier, Chantal
Rozec, Bertrand
Lauzier, Benjamin
O-GlcNAc stimulation: A new metabolic approach to treat septic shock
title O-GlcNAc stimulation: A new metabolic approach to treat septic shock
title_full O-GlcNAc stimulation: A new metabolic approach to treat septic shock
title_fullStr O-GlcNAc stimulation: A new metabolic approach to treat septic shock
title_full_unstemmed O-GlcNAc stimulation: A new metabolic approach to treat septic shock
title_short O-GlcNAc stimulation: A new metabolic approach to treat septic shock
title_sort o-glcnac stimulation: a new metabolic approach to treat septic shock
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904741/
https://www.ncbi.nlm.nih.gov/pubmed/31822776
http://dx.doi.org/10.1038/s41598-019-55381-7
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