Alteration in circulating metabolites during and after heat stress in the conscious rat: potential biomarkers of exposure and organ-specific injury

• Published in: BMC physiology Vol. 14; no. 1; p. 14
• Main Authors: Ippolito, Danielle L, Lewis, John A, Yu, Chenggang, Leon, Lisa R, Stallings, Jonathan D
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 24-12-2014; BioMed Central
• Subjects: Alkaloids; Analysis; Animals; Bile; Bile acids; Biomarkers - blood; Body Temperature Regulation; Cell Death; Heart Injuries - metabolism; Heat Exhaustion - blood; Heat Exhaustion - pathology; Heat-Shock Response; Heatstroke; Kidney - injuries; Kidney - metabolism; Liver - injuries; Liver - metabolism; Lung Injury - metabolism; Male; Mass spectrometry; Medical research; Metabolites; Metabolomics; Oxidative Stress; Rats; Rats, Inbred F344; Reactive Oxygen Species - blood; Studies; United States > US
• ISSN: 1472-6793; 1472-6793
• DOI: 10.1186/s12899-014-0014-0

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.
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, β-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.
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.