» Articles » PMID: 30745875

The Systemic Alterations of Lipids, Alanine-Glucose Cycle and Inter-Organ Amino Acid Metabolism in Swine Model Confirms the Role of Liver in Early Phase of Septic Shock

Overview
Journal Front Physiol
Date 2019 Feb 13
PMID 30745875
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Septic shock is a medical emergency and is one of the main causes of mortality in critically ill patients. Given the pathophysiological complexity of sepsis spectrum and progression in clinical settings, animal models become essential tools to improve patient care, and to understand key mechanisms that may remain masked from the heterogeneity of clinical practice. Our aim was to verify whether the metabolic constellations we previously reported for septic shock patients appear also in our septic shock swine model as systemic markers of early disturbances in energy metabolism and hepatic homeostasis. Septic shock was induced in anesthetized, instrumented, and ventilated adult swines by polymicrobial peritonitis. Hemodynamic and serial measurements of arterial and mixed venous blood gasses were made. Laboratory measurements and mass spectrometry-based targeted quantitative plasma metabolomics were performed in blood samples collected at baseline, at shock and at fully resuscitation after fluids and vasopressors administration. Data elaboration was performed by multilevel and multivariate analysis. Changes in hemodynamic, blood chemistry, and inflammatory markers were in line with a septic shock phenotype. Time course alteration of systemic metabolites were characterized by marked decreased in phosphatidylcholines and lysophosphatidylcholines species, altered alanine-glucose cycle and inter-organ amino acid metabolism, pointing toward an early hepatic impairment similarly to what we previously reported for septic shock. This is the first study in which an experimental swine model of septic shock recapitulates the main metabolic derangements reported in a clinical setting of shock. These events occur within hours from infections and may act as early metabolic features to assist in evaluating subclinical hepatic alterations and pave the way to improve the management of septic shock.

Citing Articles

Stratification of Sepsis Patients on Admission into the Intensive Care Unit According to Differential Plasma Metabolic Phenotypes.

Lodge S, Litton E, Gray N, Ryan M, Millet O, Fear M J Proteome Res. 2024; 23(4):1328-1340.

PMID: 38513133 PMC: 11002934. DOI: 10.1021/acs.jproteome.3c00803.


Longitudinal NMR Based Serum Metabolomics to Track the Potential Serum Biomarkers of Septic Shock.

Pandey S, Azim A, Sinha N Nanotheranostics. 2023; 7(2):142-151.

PMID: 36793353 PMC: 9925348. DOI: 10.7150/ntno.79394.


A Prospective, Case-Control Study of Serum Metabolomics in Neonates with Late-Onset Sepsis and Necrotizing Enterocolitis.

Thomaidou A, Deda O, Begou O, Lioupi A, Kontou A, Gika H J Clin Med. 2022; 11(18).

PMID: 36142917 PMC: 9505627. DOI: 10.3390/jcm11185270.


Identifying potential biomarkers and therapeutic targets for dogs with sepsis using metabolomics and lipidomics analyses.

Montague B, Summers A, Bhawal R, Anderson E, Kraus-Malett S, Zhang S PLoS One. 2022; 17(7):e0271137.

PMID: 35802586 PMC: 9269464. DOI: 10.1371/journal.pone.0271137.


Metabolites Concentration in Plasma and Heart Tissue in Relation to High Sensitive Cardiac Troponin T Level in Septic Shock Pigs.

Pinto B, Ferrario M, Herpain A, Brunelli L, Bendjelid K, Carrara M Metabolites. 2022; 12(4).

PMID: 35448505 PMC: 9024493. DOI: 10.3390/metabo12040319.


References
1.
Nicholson J, Wolmarans M, Park G . The role of albumin in critical illness. Br J Anaesth. 2000; 85(4):599-610. DOI: 10.1093/bja/85.4.599. View

2.
Bruins M, Soeters P, Deutz N . Endotoxemia affects organ protein metabolism differently during prolonged feeding in pigs. J Nutr. 2000; 130(12):3003-13. DOI: 10.1093/jn/130.12.3003. View

3.
Angus D, Lidicker J, Clermont G, Carcillo J, Pinsky M . Epidemiology of severe sepsis in the United States: analysis of incidence, outcome, and associated costs of care. Crit Care Med. 2001; 29(7):1303-10. DOI: 10.1097/00003246-200107000-00002. View

4.
Bruins M, Deutz N, Soeters P . Aspects of organ protein, amino acid and glucose metabolism in a porcine model of hypermetabolic sepsis. Clin Sci (Lond). 2003; 104(2):127-41. DOI: 10.1042/CS20020275. View

5.
Esmon C . Why do animal models (sometimes) fail to mimic human sepsis?. Crit Care Med. 2004; 32(5 Suppl):S219-22. DOI: 10.1097/01.ccm.0000127036.27343.48. View