Alteration in Circulating Metabolites During and After Heat Stress in the Conscious Rat: Potential Biomarkers of Exposure and Organ-specific Injury

Abstract

Background: Heat illness is a debilitating and potentially life-threatening condition. Limited data are available to identify individuals with heat illness at greatest risk for organ damage. We recently described the transcriptomic and proteomic responses to heat injury and recovery in multiple organs in an in vivo model of conscious rats heated to a maximum core temperature of 41.8 C (Tc,Max). In this study, we examined changes in plasma metabolic networks at Tc,Max, 24, or 48 hours after the heat stress stimulus. Results: Circulating metabolites were identified by gas chromatography/mass spectrometry and liquid chromatography/tandem mass spectrometry. Bioinformatics analysis of the metabolomic data corroborated proteomics and transcriptomics data in the tissue at the pathway level, supporting modulations in metabolic networks including cell death or catabolism (pyrimidine and purine degradation, acetylation, sulfation, redox alterations and glutathione metabolism, and the urea cycle/creatinine metabolism), energetics (stasis in glycolysis and tricarboxylic acid cycle, -oxidation), cholesterol and nitric oxide metabolism, and bile acids. Hierarchical clustering identified 15 biochemicals that differentiated animals with histopathological evidence of cardiac injury at 48 hours from uninjured animals. The metabolic networks perturbed in the plasma corroborated the tissue proteomics and transcriptomics pathway data, supporting a model of irreversible cell death and decrements in energetics as key indicators of cardiac damage in response to heat stress. Conclusions: Integrating plasma metabolomics with tissue proteomics and transcriptomics supports a diagnostic approach to assessing individual susceptibility to organ injury and predicting recovery after heat stress.

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Document Details

Document Type
Technical Report
Publication Date
Dec 24, 2014
Accession Number
ADA618165

Entities

People

  • Chenggang Yu
  • Danielle L. Ippolito
  • John A. Lewis
  • Jonathan D. Stallings
  • Lisa R. Leon

Organizations

  • U.S. Army Center for Environmental Health Research

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Amino Acids
  • Anabolism
  • Bile
  • Breakpoint Temperature
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Computational Biology
  • Computational Science
  • Data Science
  • Free Radicals
  • Health Services
  • Laboratory Animals
  • Medical Personnel
  • Metabolism
  • Metabolomics
  • Statistical Analysis

Fields of Study

  • Chemistry

Readers

  • Immunology and Pathology
  • Oncology and Biomarker-Based Cancer Detection.
  • Toxicology/Environmental Toxicology

Technology Areas

  • Biotechnology