Abstract

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.

Details

Title
O-GlcNAc stimulation: A new metabolic approach to treat septic shock
Author
Ferron, Marine 1 ; Cadiet, Julien 1 ; Persello, Antoine 1 ; Prat, Valentine 1   VIAFID ORCID Logo  ; Denis, Manon 1 ; Erraud, Angélique 1 ; Aillerie, Virginie 1 ; Mevel, Mathieu 2 ; Bigot, Edith 3 ; Chatham, John C 4 ; Gauthier, Chantal 1 ; Rozec, Bertrand 5 ; Lauzier, Benjamin 1 

 l’institut du thorax, INSERM, CNRS, UNIV Nantes, Nantes, France 
 INSERM UMR 1089, Université de Nantes, CHU de Nantes, Nantes, France 
 Biochemistry Department, Laënnec Hospital, CHU Nantes, Nantes, France 
 Division of Molecular and Cellular Pathology, Birmingham, United States 
 l’institut du thorax, INSERM, CNRS, UNIV Nantes, CHU Nantes, Nantes, France 
Pages
1-13
Publication year
2019
Publication date
Dec 2019
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2323450668
Copyright
© 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.