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      Pushing arterial-venous plasma biomarkers to new heights: A model for personalised redox metabolomics?

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      a , b , c , d , d , e , d , a , b , c , f , g , a , b , c , h , c , d , e , * , for the Xtreme Alps research group
      Redox Biology
      Elsevier
      cGMP, cyclic guanosine monophosphate, CPET, cardiopulmonary exercise testing, EDTA, ethylenediaminetetraacetic acid, FRAP, ferric reducing ability of plasma, 4-HNE, 4-hydroxynonenal, H2S, hydrogen sulfide, 8-iso-PG, 8-isoprostaglandin, IC-MS, ion chromatography-mass spectrometry, LC-ESI-MS/MS, liquid chromatography-electrospray ionization-tandem mass spectrometry, NEM, N-ethylmaleimide, NO, nitric oxide, NO2-, nitrite, NO3-, nitrate, ONOO-, peroxynitrite, PaO2, arterial partial pressure of oxygen, PaCO2, arterial partial pressure of carbon dioxide, ROS, reactive oxygen species, RNS, reactive nitrogen species, RSI, reactive species interactome, RSNO, S-nitrosothiol, RSS, reactive sulfur species, RXNO, total nitroso species, SO42-, sulfate, S2O32-, thiosulfate, TFT, total free thiols, Thiols, Altitude, Hypoxia, Oxygen, Oxidative stress, Hydrogen sulfide

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          Abstract

          The chemical and functional interactions between Reactive Oxygen (ROS), Nitrogen (RNS) and Sulfur (RSS) species allow organisms to detect and respond to metabolic and environmental stressors, such as exercise and altitude exposure. Whether redox markers and constituents of this ‘Reactive Species Interactome’ (RSI) differ in concentration between arterial and venous blood is unknown. We hypothesised that such measurements may provide useful insight into metabolic/redox regulation at the whole-body level and would be consistent between individuals exposed to identical challenges. An exploratory study was performed during the Xtreme Alps expedition in 2010 in which four healthy individuals (2 male, 2 female) underwent paired arterial and central venous blood sampling before, during and after performance of a constant-work-rate cardiopulmonary exercise test, at sea level and again at 4559 m. Unexpectedly, plasma total free thiol and free cysteine concentrations remained substantially elevated at altitude throughout exercise with minimal arteriovenous gradients. Free sulfide concentrations changed only modestly upon combined altitude/exercise stress, whereas bound sulfide levels were lower at altitude than sea-level. No consistent signal indicative of the expected increased oxidative stress and nitrate→nitrite→NO reduction was observed with 4-hydroxynonenal, isoprostanes, nitrate, nitrite, nitroso species and cylic guanosine monophosphate. However, the observed arteriovenous concentration differences revealed a dynamic pattern of response that was unique to each participant. This novel redox metabolomic approach of obtaining quantifiable ‘metabolic signatures’ to a defined physiological challenge could potentially offer new avenues for personalised medicine.

          Highlights

          • Exercise and high altitude (hypobaric hypoxia) significantly perturb redox balance.

          • The role of thiols and reactive sulfur species in altitude acclimatization remains largely unknown.

          • First measure of arteriovenous gradients of redox markers at altitude.

          • Different individuals exposed to identical stresses display distinct redox response profiles.

          • Redox metabolomics may offer new ways of personalizing medicine.

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          Most cited references29

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          The cystine/glutamate antiporter system x(c)(-) in health and disease: from molecular mechanisms to novel therapeutic opportunities.

          The antiporter system x(c)(-) imports the amino acid cystine, the oxidized form of cysteine, into cells with a 1:1 counter-transport of glutamate. It is composed of a light chain, xCT, and a heavy chain, 4F2 heavy chain (4F2hc), and, thus, belongs to the family of heterodimeric amino acid transporters. Cysteine is the rate-limiting substrate for the important antioxidant glutathione (GSH) and, along with cystine, it also forms a key redox couple on its own. Glutamate is a major neurotransmitter in the central nervous system (CNS). By phylogenetic analysis, we show that system x(c)(-) is a rather evolutionarily new amino acid transport system. In addition, we summarize the current knowledge regarding the molecular mechanisms that regulate system x(c)(-), including the transcriptional regulation of the xCT light chain, posttranscriptional mechanisms, and pharmacological inhibitors of system x(c)(-). Moreover, the roles of system x(c)(-) in regulating GSH levels, the redox state of the extracellular cystine/cysteine redox couple, and extracellular glutamate levels are discussed. In vitro, glutamate-mediated system x(c)(-) inhibition leads to neuronal cell death, a paradigm called oxidative glutamate toxicity, which has successfully been used to identify neuroprotective compounds. In vivo, xCT has a rather restricted expression pattern with the highest levels in the CNS and parts of the immune system. System x(c)(-) is also present in the eye. Moreover, an elevated expression of xCT has been reported in cancer. We highlight the diverse roles of system x(c)(-) in the regulation of the immune response, in various aspects of cancer and in the eye and the CNS.
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            Oxygen radicals, nitric oxide, and peroxynitrite: Redox pathways in molecular medicine

            Aerobic life in humans imposes the hazard of excess oxidation in cell and tissue components that may compromise cell function and viability. The formation and accumulation of oxidized products in biomolecules such as proteins and lipids are observed in various pathologies and during the normal aging process. This review article aims to integrate some early and remarkable discoveries in the field, with more recent developments that helped to define a causative role of oxygen radicals, nitric oxide, and peroxynitrite in human physiology and pathology. These aspects of human redox biochemistry contribute to the understanding of the molecular basis of diseases and aging and open avenues for the development of preventive and therapeutic strategies in molecular medicine. Oxygen-derived free radicals and related oxidants are ubiquitous and short-lived intermediates formed in aerobic organisms throughout life. These reactive species participate in redox reactions leading to oxidative modifications in biomolecules, among which proteins and lipids are preferential targets. Despite a broad array of enzymatic and nonenzymatic antioxidant systems in mammalian cells and microbes, excess oxidant formation causes accumulation of new products that may compromise cell function and structure leading to cell degeneration and death. Oxidative events are associated with pathological conditions and the process of normal aging. Notably, physiological levels of oxidants also modulate cellular functions via homeostatic redox-sensitive cell signaling cascades. On the other hand, nitric oxide ( • NO), a free radical and weak oxidant, represents a master physiological regulator via reversible interactions with heme proteins. The bioavailability and actions of • NO are modulated by its fast reaction with superoxide radical ( O 2 • − ), which yields an unusual and reactive peroxide, peroxynitrite, representing the merging of the oxygen radicals and • NO pathways. In this Inaugural Article, I summarize early and remarkable developments in free radical biochemistry and the later evolution of the field toward molecular medicine; this transition includes our contributions disclosing the relationship of • NO with redox intermediates and metabolism. The biochemical characterization, identification, and quantitation of peroxynitrite and its role in disease processes have concentrated much of our attention. Being a mediator of protein oxidation and nitration, lipid peroxidation, mitochondrial dysfunction, and cell death, peroxynitrite represents both a pathophysiologically relevant endogenous cytotoxin and a cytotoxic effector against invading pathogens.
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              The Reactive Species Interactome: Evolutionary Emergence, Biological Significance, and Opportunities for Redox Metabolomics and Personalized Medicine

              Abstract Significance: Oxidative stress is thought to account for aberrant redox homeostasis and contribute to aging and disease. However, more often than not, administration of antioxidants is ineffective, suggesting that our current understanding of the underlying regulatory processes is incomplete. Recent Advances: Similar to reactive oxygen species and reactive nitrogen species, reactive sulfur species are now emerging as important signaling molecules, targeting regulatory cysteine redox switches in proteins, affecting gene regulation, ion transport, intermediary metabolism, and mitochondrial function. To rationalize the complexity of chemical interactions of reactive species with themselves and their targets and help define their role in systemic metabolic control, we here introduce a novel integrative concept defined as the reactive species interactome (RSI). The RSI is a primeval multilevel redox regulatory system whose architecture, together with the physicochemical characteristics of its constituents, allows efficient sensing and rapid adaptation to environmental changes and various other stressors to enhance fitness and resilience at the local and whole-organism level. Critical Issues: To better characterize the RSI-related processes that determine fluxes through specific pathways and enable integration, it is necessary to disentangle the chemical biology and activity of reactive species (including precursors and reaction products), their targets, communication systems, and effects on cellular, organ, and whole-organism bioenergetics using system-level/network analyses. Future Directions: Understanding the mechanisms through which the RSI operates will enable a better appreciation of the possibilities to modulate the entire biological system; moreover, unveiling molecular signatures that characterize specific environmental challenges or other forms of stress will provide new prevention/intervention opportunities for personalized medicine. Antioxid. Redox Signal. 27, 684–712.
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                Author and article information

                Contributors
                Journal
                Redox Biol
                Redox Biol
                Redox Biology
                Elsevier
                2213-2317
                22 January 2019
                February 2019
                22 January 2019
                : 21
                : 101113
                Affiliations
                [a ]Critical Care Research Group, Southampton NIHR Biomedical Research Centre, Tremona Road, Southampton SO16 6YD, UK
                [b ]Anaesthesia and Critical Care Research Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton SO16 6YD, UK
                [c ]Integrative Physiology and Critical Illness Group, Clinical and Experimental Sciences, University of Southampton, Tremona Road, Southampton SO16 6YD, UK
                [d ]Clinical & Experimental Sciences, Faculty of Medicine, NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton SO16 6YD, UK
                [e ]Warwick Medical School, Division of Metabolic and Vascular Health, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, UK
                [f ]UCL Centre for Altitude, Space and Extreme Environment (CASE) Medicine, UCLH NIHR Biomedical Research Centre, Institute of Sport Exercise & Health, 170 Tottenham Court Road, London W1T 7HA, UK
                [g ]Intensive Care Unit, Royal Free Hospital, Pond Street, London NW3 2QG, UK
                [h ]Department of Anesthesiology, Duke University Medical School, NC, USA
                Author notes
                [* ]Corresponding author at: Integrative Physiology and Critical Illness Group, Clinical and Experimental Sciences, University of Southampton, Tremona Road, Southampton SO16 6YD, UK. m.feelisch@ 123456soton.ac.uk
                Article
                S2213-2317(18)31082-6 101113
                10.1016/j.redox.2019.101113
                6369731
                30738322
                e0f59798-d2e2-43e7-b426-eec2af03e56a
                © 2019 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 November 2018
                : 4 January 2019
                : 14 January 2019
                Categories
                Short Communication

                cgmp, cyclic guanosine monophosphate,cpet, cardiopulmonary exercise testing,edta, ethylenediaminetetraacetic acid,frap, ferric reducing ability of plasma,4-hne, 4-hydroxynonenal,h2s, hydrogen sulfide,8-iso-pg, 8-isoprostaglandin,ic-ms, ion chromatography-mass spectrometry,lc-esi-ms/ms, liquid chromatography-electrospray ionization-tandem mass spectrometry,nem, n-ethylmaleimide,no, nitric oxide,no2-, nitrite,no3-, nitrate,onoo-, peroxynitrite,pao2, arterial partial pressure of oxygen,paco2, arterial partial pressure of carbon dioxide,ros, reactive oxygen species,rns, reactive nitrogen species,rsi, reactive species interactome,rsno, s-nitrosothiol,rss, reactive sulfur species,rxno, total nitroso species,so42-, sulfate,s2o32-, thiosulfate,tft, total free thiols,thiols,altitude,hypoxia,oxygen,oxidative stress,hydrogen sulfide

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