Résumé
L’oxygène est un composé structurel et fonctionnel indispensable á la vie. Évoquer la toxicité de cette molécule essentielle peut paraÎtre inapproprié voire provocateur. Pourtant, peu après sa découverte par Priestley en 1774, le nom d’oxygène lui fut donné par Lavoisier á partir du grec oxys et gennan signifiant « qui génère de l’acide ». Dans le même temps, ce dernier mettait en évidence son rôle essentiel dans la respiration. Cela soulignait d’emblée la dualité de cette molécule á laquelle le vivant a dû s’adapter. En effet, dans certaines conditions particulières, l’oxygène peut s’avérer délétère en raison de son caractère oxydant.
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Références
Favier A (2006) Stress oxydant et pathologie humaine. Ann Pharm Fr 64: 390–6
Kohen R, Nyska A (2002) Oxidation of biological systems: oxidative stress phenomena, antioxidants, redox reactions, and methods for their quantification. Toxicol Pathol 30: 620–50
Droge W (2002) Free radicals in the physiological control of cell function. Physiol Rev 82: 47–95
Levraut J, Iwase H, Shao ZH, Vanden Hoek TL, Schumacker PT (2003) Cell death during ischemia: relationship to mitochondrial depolarization and ROS generation. Am J Physiol Heart Circ Physiol 284: 549–58
Piper HM, Garcia-Dorado D, Ovize M (1998) A fresh look at reperfusion injury. Cardiovasc Res 38: 291–300
Vanden Hoek TL (2002) Preconditioning and postresuscitation injury. Crit Care Med 30: S172–5
Dahlgren C, Karlsson A (1999) Respiratory burst in human neutrophils. J Immunol Methods 232: 3–14
Lebuffe G, Schumacker PT, Shao ZH, Anderson T, Iwase H, Vanden Hoek TL (2003) ROS and NO trigger early preconditioning: relationship to mitochondrial KATP channel. Am J Physiol Heart Circ Physiol 284: H299–308
Halliwell B, Gutteridge JM (1988) Free radicals and antioxidants protection: mechanisms and significance in toxicology and disease. Hum Toxicol 7: 7–13
Fridovich I (1995) Superoxide radical and superoxide dismutases. Ann Rev Biochem 64: 97–112
Richier S, Merle PL, Furla P, Pigozzi D, Sola F, Allemand D (2003) Characterization of superoxide dismutases in anoxia-and hyperoxia-tolerant symbiotic cnidarians. Biochim Biophys Acta 1621: 84–91
Schnackenberg CG, Welch WJ, Wilcox CS (1998) Normalization of blood pressure and renal vascular resistance in SHR with a membrane-permeable superoxide dismutase mimetic: role of nitric oxide. Hypertension 32: 59–64
Kirkman HN, Rolfo M, Ferraris AM, Gaetani GF (1999) Mechanisms of protection of catalase by NADPH. Kinetics and stoichiometry. J Biol Chem 274: 13908–14
Giacco F, Brownlee M (2010) Oxidative stress and diabetic complications. Circ Res 107: 1058–70
Briones AM, Touyz RM (2010) Oxidative stress and hypertension: current concepts. Curr Hypertens Rep 12: 135–42
Khaper N, Bryan S, Dhingra S et al. (2010) Targeting the vicious inflammation-oxidative stress cycle for the management of heart failure. Antioxid Redox Signal 13: 1033–49
Romano AD, Serviddio G, de Matthaeis A, Bellanti F, Vendemiale G (2010) Oxidative stress and aging. J Nephrol 23: S29–36
Laplace C, Huet O, Vicaut E, Ract C, Martin L, Benhamou D, Duranteau J (2005) Endothelial oxidative stress induced by serum from patients with severe trauma hemorrhage. Intensive Care Med 31: 1174–80
Huet O, Obata R, Aubron C et al. (2007) Plasma-induced endothelial oxidative stress is related to the severity of septic shock. Crit Care Med 35: 821–6
Fläring UB, Rooyackers OE, Hebert C, Bratel T, Hammarqvist F, Wernerman J (2005) Temporal changes in whole-blood and plasma glutathione in ICU patients with multiple organ failure. Intensive Care Med 31: 1072–8
Motoyama T, Okamoto K, Kukita I, Hamaguchi M, Kinoshita Y, Ogawa H (2003) Possible role of increased oxidant stress in multiple organ failure after systemic inflammatory response syndrome. Crit Care Med 31: 1048–52
Carpenter CT, Price PV, Christman BW (1998) Exhaled breath condensate isoprostanes are elevated in patients with acute lung injury or ARDS. Chest 114: 1653–9
Quinlan GJ, Lamb NJ, Evans TW, Gutteridge JM (1996) Plasma fatty acid changes and increased lipid peroxidation in patients with adult respiratory distress syndrome. Crit Care Med 24: 241–6
Lamb NJ, Quinlan GJ, Westerman ST, Gutteridge JM, Evans TW (1999) Nitration of proteins in bronchoalveolar lavage fluid from patients with acute respiratory distress syndrome receiving inhaled nitric oxide. Am J Respir Crit Care Med 160: 1031–4
Quinlan GJ, Mumby S, Martin GS, Bernard GR, Gutteridge JM, Evans TW (2004) Albumin influences total plasma antioxidant capacity favorably in patients with acute lung injury. Crit Care Med 32: 755–9
Asano T (1999) Oxyhemoglobin as the principal cause of cerebral vasospasm: a holistic view of its actions. Crit Rev Neurosurg 24: 303–18
Polidori MC, Mecocci P, Frei B (2001) Plasma vitamin C levels are decreased and correlated with brain damage in patients with intracranial hemorrhage or head trauma. Stroke 32: 898–902
Gaetani P, Pasqualin A, Rodriguez y Baena R, Borasio E, Marzatico F (1998) Oxidative stress in the human brain after subarachnoid hemorrhage. J Neurosurg 89: 748–54
Déroche D, Orban JC, Garrel C, Ferrari P, Levraut J, Ichai C (2009) Evaluation du stress oxydant après cardiaque extra-hospitalier traité par hypothermie. Ann Fr Anesth Réanim 28: S170
Kilgannon JH, Jones AE, Shapiro NI et al.; Emergency Medicine Shock Research Network (EMShockNet) Investigators (2010) Association between arterial hyperoxia following resuscitation from cardiac arrest and in-hospital mortality. JAMA 303: 2165–71
Mathru M, Dries DJ, Barnes L, Tonino P, Sukhani R, Rooney MW (1996) Tourniquet-induced exsanguination in patients requiring lower limb surgery. An ischemia-reperfusion model of oxidant and antioxidant metabolism. Anesthesiology 84: 14–22
Kretzschmar M, Klein U, Palutke M, Schirrmeister W (1996) Reduction of ischemia-reperfusion syndrome after abdominal aortic aneurysmectomy by N-acetylcysteine but not mannitol. Acta Anaesthesiol Scand 40: 657–64
Basu S, Meisert I, Eggensperger E, Krieger E, Krenn CG (2007) Time course and attenuation of ischaemia-reperfusion induced oxidative injury by propofol in human renal transplantation. Redox Rep 12: 195–202
Biernacki M, Bigda J, Jankowski K, Wozniak M, Sledziński Z (2002) Increased serum levels of markers of oxidative stress during kidney transplantation. Transplant Proc 34: 544–5
Hassan L, Bueno P, Ferrón-Celma I et al. (2005) Time course of antioxidant enzyme activities in liver transplant recipients. Transplant Proc 37: 3932–5
Emet S, Memis D, Pamukçu Z (2004) The influence of N-acetyl-L-cystein infusion on cytokine levels and gastric intramucosal pH during severe sepsis. Crit Care 8: 172–9
Spapen H, Zhang H, Demanet C, Vleminckx W, Vincent JL, Huyghens L (1998) Does N-acetyl-L-cysteine influence cytokine response during early human septic shock? Chest 113: 1616–24
Ortolani O, Conti A, De Gaudio AR, Moraldi E, Cantini Q, Novelli G (2000) The effect of glutathione and N-acetylcysteine on lipoperoxidative damage in patients with early septic shock. Am J Respir Crit Care Med 161: 1907–11
Tepel M, van der Giet M, Schwarzfeld C, Laufer U, Liermann D, Zidek W (2000) Prevention of radiographic-contrast-agent-induced reductions in renal function by acetylcysteine. N Engl J Med 343: 180–4
Ho KM, Morgan DJ (2009) Meta-analysis of N-acetylcysteine to prevent acute renal failure after major surgery. Am J Kidney Dis 53: 33–40
Crimi E, Liguori A, Condorelli M et al. (2004) The beneficial effects of antioxidant supplementation in enteral feeding in critically ill patients: a prospective, randomized, double-blind, placebo-controlled trial. Anesth Analg 99: 857–63
Nathens AB, Neff MJ, Jurkovich GJ et al. (2002) Randomized, prospective trial of antioxidant supplementation in critically ill surgical patients. Ann Surg 236: 814–22
Collier BR, Giladi A, Dossett LA, Dyer L, Fleming SB, Cotton BA (2008) Impact of high-dose antioxidants on outcomes in acutely injured patients. JPEN J Parenter Enteral Nutr 3: 384–8
Cheng YJ, Wang YP, Chien CT, Chen CF (2002) Small-dose propofol sedation attenuates the formation of reactive oxygen species in tourniquet-induced ischemia-reperfusion injury under spinal anesthesia. Anesth Analg 94: 1617–20
Vanden Hoek T, Becker LB, Shao ZH, Li CQ, Schumacker PT (2000) Preconditioning in cardiomyocytes protects by attenuating oxidant stress at reperfusion. Circ Res 86: 541–8
Murry CE, Jennings RB, Reimer KA (1986) Preconditioning with ischemia: a delay of lethal cell injury in ischemic myocardium. Circulation 74: 1124–36
Wu ZK, Tarkka MR, Pehkonen E, Kaukinen L, Honkonen EL, Kaukinen S (2000) Ischaemic preconditioning has a beneficial effect on left ventricular haemodynamic function after a coronary artery biopass grafting operation. Scand Cardiovasc J 34: 247–53
Wu ZK, Iivainen T, Pehkonen E, Laurikka J, Tarkka MR (2002) Ischemic preconditioning suppresses ventricular tachyarrhythmias after myocardial revascularization. Circulation 106: 3091–6
Hausenloy DJ, Mwamure PK, Venugopal V et al. (2007) Effect of remote ischaemic preconditioning on myocardial injury in patients undergoing coronary artery bypass graft surgery: a randomised controlled trial. Lancet 370: 575–9
Zaugg M, Lucchinetti E, Spahn DR, Pasch T, Schaub MC (2002) Volatile anesthetics mimic cardiac preconditioning by priming the activation of mitochondrial K(ATP) channels via multiple signaling pathways. Anesthesiology 97: 4–14
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Orban, JC. (2011). Oxygène, stress oxydant. In: Désordres métaboliques et réanimation. Le point sur .... Springer, Paris. https://doi.org/10.1007/978-2-287-99027-4_22
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