Exploratory proteomic analysis of hypobaric hypoxia and acute mountain sickness in humans

• Published in: Journal of applied physiology (1985) 2014-04, Vol.116 (7), p.937-944
• Main Authors: Julian, Colleen G, Subudhi, Andrew W, Hill, Ryan C, Wilson, Megan J, Dimmen, Andrew C, Hansen, Kirk C, Roach, Robert C
• Format: Article
• Language: English
• Subjects: Acclimatization; Acute Disease; Adult; Altitude; Altitude Sickness - blood; Altitude Sickness - diagnosis; Antioxidants - metabolism; Biomarkers; Biomarkers - blood; Blood Proteins - metabolism; Case-Control Studies; Chromatography, High Pressure Liquid; Enzymes - blood; Female; Highlighted Topic; Human subjects; Humans; Hypoxia; Hypoxia - blood; Hypoxia - diagnosis; Male; Motion sickness; Oxidation-Reduction; Oxidative Stress; Physiology; Proteins; Proteomics; Proteomics - methods; Tandem Mass Spectrometry; Time Factors
• ISSN: 8750-7587; 1522-1601
• DOI: 10.1152/japplphysiol.00362.2013

Our objective in this exploratory study was to identify novel biomarkers of importance for acute mountain sickness (AMS) using discovery-based proteomic methods. Peripheral blood samples were collected and AMS symptoms were assessed in 20 healthy volunteers prior to [-15 h (baseline) and 0 h; 1,609 m; barometric pressure = 625 mmHg] and after a 9-h exposure to hypobaric hypoxia (9 h; 4,875 m; barometric pressure = 425 mmHg). AMS status was assessed using the Lake Louise Questionnaire. Plasma samples were pooled according to AMS status at each time point. Protein composition of the samples was determined by a GeLC-MS/MS approach using two analytical platforms (LTQ-XL linear ion trap mass spectrometer and a LTQ-FT ultra hybrid mass spectrometer) for technical replication. Spectral counting was used to make semiquantitative comparisons of protein abundance between AMS-susceptible (AMS) and AMS-resistant (AMS·R) subjects with exposure to hypobaric hypoxia. After 9 h of hypoxia, the abundance of proteins with antioxidant properties (i.e., peroxiredoxin 6, glutathione peroxidase, and sulfhydryl oxidase 1) rose in AMS but not AMS·R. Our exploratory analyses suggest that exposure to hypobaric hypoxia enhances enzymatic antioxidant systems in AMS vs. AMS·R, which, we propose, may be an overcompensation for hypoxia-induced oxidant production. On the basis of our findings we 1) speculate that quenching oxidant activity may have adverse downstream effects that are of pathophysiological importance for AMS such as interrupting oxidant-sensitive cell signaling and gene transcription and 2) question the existing assumption that increased oxidant production in AMS is pathological.