Protective effect of ozone treatment on the injury associated with hepatic ischemia-reperfusion: antioxidant-prooxidant balance.

The effects of ozone treatment on the injury associated to hepatic ischemia-reperfusion (I/R) was evaluated. Ozone treatment (1 mg/kg daily during 10 days by rectal insufflation) is shown to be protective as it attenuated the increases in transaminases (AST, ALT) and lactate levels observed after I/R. I/R leads to a decrease in endogenous antioxidant (SOD and glutathione) and an increase in reactive oxygen species (H2O2) with respect to the control group. However, ozone treatment results in a preservation (glutathione) or increase (SOD) in antioxidant defense and maintains H2O2 at levels comparable to those in the control group. The present study reports a protective effect of ozone treatment on the injury associated to hepatic I/R. The effectiveness of ozone could be related to its action on endogenous antioxidants and prooxidants balance in favour of antioxidants, thus attenuating oxidative stress.

[1]  M. Menger,et al.  Hepatic microcirculatory perfusion failure is a determinant of liver dysfunction in warm ischemia-reperfusion. , 1994, The American journal of pathology.

[2]  L. Oberley,et al.  Redox gene therapy for ischemia/reperfusion injury of the liver reduces AP1 and NF-κB activation , 1998, Nature Medicine.

[3]  D. Hinshaw,et al.  Oxidant stress: the role of the glutathione redox cycle in skin preconditioning. , 1995, The Journal of surgical research.

[4]  J. Gavin,et al.  Fine structural changes in dog myocardium exposed to lowered pH in vivo. , 1977, Laboratory investigation; a journal of technical methods and pathology.

[5]  R. Castillo,et al.  Ozone oxidative preconditioning: a protection against cellular damage by free radicals. , 1998, Mediators of Inflammation.

[6]  F Hernández,et al.  Decrease of blood cholesterol and stimulation of antioxidative response in cardiopathy patients treated with endovenous ozone therapy. , 1995, Free radical biology & medicine.

[7]  J. Nunn,et al.  Molecular structure of free radicals and their importance in biological reactions. , 1988, British journal of anaesthesia.

[8]  H. Rosenberg,et al.  Histopathology of the Conduction System in the Sudden Infant Death Syndrome , 1976, Circulation.

[9]  J. McAnulty,et al.  Oxygen-derived free radical damage in organ preservation: activity of superoxide dismutase and xanthine oxidase. , 1987, Surgery.

[10]  J. Roselló-Catafau,et al.  Protective effect of preconditioning on the injury associated to hepatic ischemia‐reperfusion in the rat: Role of nitric oxide and adenosine , 1997, Hepatology.

[11]  J. McCord,et al.  Oxygen-derived free radicals in postischemic tissue injury. , 1985, The New England journal of medicine.

[12]  S. Marklund Properties of extracellular superoxide dismutase from human lung. , 1984, The Biochemical journal.

[13]  Keiichiro Suzuki,et al.  Sublethal ischemia alters myocardial antioxidant activity in canine heart. , 1993, The American journal of physiology.

[14]  H. Sies,et al.  Identification and quantitation of glutathione in hepatic protein mixed disulfides and its relationship to glutathione disulfide. , 1983, Biochemical pharmacology.

[15]  V. Bocci Ozone as a bioregulator. Pharmacology and toxicology of ozonetherapy today. , 1996, Journal of biological regulators and homeostatic agents.

[16]  R Mohabir,et al.  Effects of ischemia and hypercarbic acidosis on myocyte calcium transients, contraction, and pHi in perfused rabbit hearts. , 1991, Circulation research.

[17]  H. Sies Oxidative stress: from basic research to clinical application. , 1991, The American journal of medicine.

[18]  B. Safer,et al.  Contribution of tissue acidosis to ischemic injury in the perfused rat heart. , 1976, Circulation.

[19]  R. Weiss,et al.  Importance of metabolic inhibition and cellular pH in mediating preconditioning contractile and metabolic effects in rat hearts. , 1994, Circulation research.

[20]  M. Hori,et al.  Delayed effects of sublethal ischemia on the acquisition of tolerance to ischemia. , 1993, Circulation research.

[21]  M. Lamy,et al.  Antioxidant defense and free radical production in a rabbit model of kidney ischemia-reperfusion. , 1995, Transplantation proceedings.

[22]  N. Khaper,et al.  Hydrogen peroxide changes in ischemic and reperfused heart. Cytochemistry and biochemical and X-ray microanalysis. , 1995, The American journal of pathology.

[23]  R. Hinder,et al.  Oxygen free radicals and glutathione in hepatic ischemia/reperfusion injury. , 1991, The Journal of surgical research.

[24]  M. Martínez-Cayuela Oxygen free radicals and human disease. , 1995, Biochimie.

[25]  J. Engelhardt,et al.  Redox gene therapy of liver ischemia/reperfusion injury reduces AP-1 and NF-KB activation , 1998 .

[26]  J. McCord,et al.  Superoxide radicals in feline intestinal ischemia. , 1981, Gastroenterology.

[27]  Farber Jl Biology of disease: membrane injury and calcium homeostasis in the pathogenesis of coagulative necrosis. , 1982, Laboratory investigation; a journal of technical methods and pathology.

[28]  L. Toledo-Pereyra,et al.  INFLUENCE OF OXYGEN‐DERIVED FREE RADICAL SCAVENGERS ON ISCHEMIC LIVERS , 1985, Transplantation.

[29]  M. Tani,et al.  Role of Intracellular Na+ in Ca2+ Overload and Depressed Recovery of Ventricular Function of Reperfused Ischemic Rat Hearts Possible Involvement of H+-Na+ and Na+-Ca2+ Exchange , 1989, Circulation research.