Literature DB >> 31439155

Identification of Metabolic Changes in Ileum, Jejunum, Skeletal Muscle, Liver, and Lung in a Continuous I.V. Pseudomonas aeruginosa Model of Sepsis Using Nontargeted Metabolomics Analysis.

Amro Ilaiwy1, Gabriella A M Ten Have2, James R Bain1, Michael J Muehlbauer3, Sara K O'Neal3, Jessica M Berthiaume4, Traci L Parry4, Nicolaas E Deutz2, Monte S Willis5.   

Abstract

Sepsis is a multiorgan disease affecting the ileum and jejunum (small intestine), liver, skeletal muscle, and lung clinically. The specific metabolic changes in the ileum, jejunum, liver, skeletal muscle, and lung have not previously been investigated. Live Pseudomonas aeruginosa, isolated from a patient, was given via i.v. catheter to pigs to induce severe sepsis. Eighteen hours later, ileum, jejunum, medial gastrocnemius skeletal muscle, liver, and lung were analyzed by nontargeted metabolomics analysis using gas chromatography/mass spectrometry. The ileum and the liver demonstrated significant changes in metabolites involved in linoleic acid metabolism: the ileum and lung had significant changes in the metabolism of valine/leucine/isoleucine; the jejunum, skeletal muscle, and liver had significant changes in arginine/proline metabolism; and the skeletal muscle and lung had significant changes in aminoacyl-tRNA biosynthesis, as analyzed by pathway analysis. Pathway analysis also identified changes in metabolic pathways unique for different tissues, including changes in the citric acid cycle (jejunum), β-alanine metabolism (skeletal muscle), and purine metabolism (liver). These findings demonstrate both overlapping metabolic pathways affected in different tissues and those that are unique to others and provide insight into the metabolic changes in sepsis leading to organ dysfunction. This may allow therapeutic interventions that focus on multiple tissues or single tissues once the relationship of the altered metabolites/metabolism to the underlying pathogenesis of sepsis is determined.
Copyright © 2019 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31439155      PMCID: PMC6723233          DOI: 10.1016/j.ajpath.2019.05.021

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  92 in total

1.  Technical advance: simultaneous analysis of metabolites in potato tuber by gas chromatography-mass spectrometry.

Authors:  U Roessner; C Wagner; J Kopka; R N Trethewey; L Willmitzer
Journal:  Plant J       Date:  2000-07       Impact factor: 6.417

2.  In vivo measurement of nitric oxide production in porcine gut, liver and muscle during hyperdynamic endotoxaemia.

Authors:  Maaike J Bruins; Wouter H Lamers; Alfred J Meijer; Peter B Soeters; Nicolaas E P Deutz
Journal:  Br J Pharmacol       Date:  2002-12       Impact factor: 8.739

Review 3.  Intestinal epithelial hyperpermeability: update on the pathogenesis of gut mucosal barrier dysfunction in critical illness.

Authors:  Mitchell P Fink
Journal:  Curr Opin Crit Care       Date:  2003-04       Impact factor: 3.687

4.  Deconvolution gas chromatography/mass spectrometry of urinary organic acids--potential for pattern recognition and automated identification of metabolic disorders.

Authors:  J M Halket; A Przyborowska; S E Stein; W G Mallard; S Down; R A Chalmers
Journal:  Rapid Commun Mass Spectrom       Date:  1999       Impact factor: 2.419

5.  L-arginine supplementation in pigs decreases liver protein turnover and increases hindquarter protein turnover both during and after endotoxemia.

Authors:  Maaike J Bruins; Peter B Soeters; Wouter H Lamers; Nicolaas E P Deutz
Journal:  Am J Clin Nutr       Date:  2002-06       Impact factor: 7.045

6.  L-arginine supplementation in hyperdynamic endotoxemic pigs: effect on nitric oxide synthesis by the different organs.

Authors:  Maaike J Bruins; Peter B Soeters; Wouter H Lamers; Alfred J Meijer; Nicolaas E P Deutz
Journal:  Crit Care Med       Date:  2002-03       Impact factor: 7.598

Review 7.  Mitochondrial dysfunction in sepsis.

Authors:  M Singer; D Brealey
Journal:  Biochem Soc Symp       Date:  1999

8.  Endotoxemia affects organ protein metabolism differently during prolonged feeding in pigs.

Authors:  M J Bruins; P B Soeters; N E Deutz
Journal:  J Nutr       Date:  2000-12       Impact factor: 4.798

9.  Effect of prolonged hyperdynamic endotoxemia on jejunal motility in fasted and enterally fed pigs.

Authors:  Maaike J Bruins; Yvette C Luiking; Peter B Soeters; Louis M A Akkermans; Nicolaas E P Deutz
Journal:  Ann Surg       Date:  2003-01       Impact factor: 12.969

10.  Aspects of organ protein, amino acid and glucose metabolism in a porcine model of hypermetabolic sepsis.

Authors:  Maaike J Bruins; Nicolaas E P Deutz; Peter B Soeters
Journal:  Clin Sci (Lond)       Date:  2003-02       Impact factor: 6.124

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Journal:  J Pers Med       Date:  2022-04-02

2.  The multiomics landscape of serum exosomes during the development of sepsis.

Authors:  Lei Li; Lin Huang; Chenyang Huang; Jia Xu; Yukai Huang; Haihua Luo; Xinya Lu; Shuyue He; Gang Yuan; Li Chen; Xue Han; Xusong Cao; Aolin Jiang; Cuiting Liu; Junmin Shi; Hong Yang; Yong Jiang
Journal:  J Adv Res       Date:  2021-11-17       Impact factor: 12.822

3.  Estrogen-Related Receptor γ Agonist DY131 Ameliorates Lipopolysaccharide-Induced Acute Liver Injury.

Authors:  Haoyang Ma; Jiaye Liu; Yang Du; Shengnan Zhang; Weidong Cao; Zhanjun Jia; Wei Gong; Aihua Zhang
Journal:  Front Pharmacol       Date:  2021-04-23       Impact factor: 5.810

4.  Dichloroacetate reverses sepsis-induced hepatic metabolic dysfunction.

Authors:  Rabina Mainali; Manal Zabalawi; David Long; Nancy Buechler; Ellen Quillen; Chia-Chi Key; Xuewei Zhu; John S Parks; Cristina Furdui; Peter W Stacpoole; Jennifer Martinez; Charles E McCall; Matthew A Quinn
Journal:  Elife       Date:  2021-02-22       Impact factor: 8.140

  4 in total

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