Abstract
The confirmed advantageous effects of oxygen/ozone therapy in several clinical conditions stimulated experimental studies on effects of the therapy in rats with an induced septic shock. The studies were conducted on adult male rats of Wistar strain. Four groups of the animals, each of 15 rats, included: I—control group, (C); II—animals intraperitoneally administered with O2/O3 (CO), III—rats given of Escherichia coli endotoxin (lipopolysaccharide—LPS) (CL), IV—rats administered with the lipopolysaccharide plus administered with the oxygen/ozone mixture (OL). Activities of catalase and superoxide dismutase and of free radical reactions were estimated. The exposure to LPS augmented activities of SOD and of catalase in liver, lungs and heart. In all the examined organs LPS induced significant changes in levels of free radicals. Except of the lungs, parallel administration of the rats with LPS and ozone/oxygen revoked development of the alterations. The obtained results point to a strong, stabilizing and regenerative effect of ozonotherapy.
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Barriere, S. L., and J. B. Guglielmo. 1992. Gram-negative sepsis, the sepsis syndrome and the role of antiendotoxin monoclonal antibodies. Clin. Pharm. 11:223–232.
Madej, P., Z. Antoszewski, and J. A. Madej. 1995. Ozonotherapy. Mater Med. Pol. 27:53–56.
Laszczyca, P., E. Kawka-Serwecinska, I. Witas, B. Dolezych, B. Falkus, A. Mekail, B. Ziolkowska, P. Madej, and P. Migula. 1996. Lipid peroxidation and activity of antioxidative enzymes in the rat model of ozone therapy. Mater Med. Pol. 28:155–160.
Leon, O. S., S. Menendez, N. Merino, R. Castillo, S. Sam, L. Perez, E. Cruz, and V. Bocci. 1998. Ozone oxidative preconditioning: a protection against cellular damage by free radicals. Mediat. Inflamm. 7:289–294.
Barber, E., S. Menendez, O. S. Leon, M. O. Barber, N. Merino, J. L. Calunga, E. Cruz, and V. Bocci. 1999. Prevention of renal injury after induction of ozone tolerance in rats submitted to warm ischaemia. Mediat. Inflamm. 8:37–41.
Fridovich, I. 1976. Superoxide dismutases: studies of structure and mechanism. Adv. Exp. Med. Biol. 74:530–539.
Yim, M. B., P. B. Chock, and E. R. Stadtman. 1993. Enzyme function of copper, zinc superoxide dismutase as a free radical generator. J. Biol. Chem. 268:4099–4105.
Geller, B. L., and D. R. Winge. 1982. Rat liver Cu,Zn-superoxide dismutase. Subcellular location in lysosomes. J. Biol. Chem. 257:8945–8952.
Boveris, A., S. Alvarez, and A. Navarro. 2002. The role of mitochondrial nitric oxide synthase in inflammation and septic shock. Free Radic. Biol. Med. 33:1186–1193.
Hirata, Y., and S. Ishimaru. 2002. Effects of endothelin receptor antagonists on endothelin-1 and inducible nitric oxide synthase genes in a rat endotoxic shock model. Clin. Sci. (Lond) 103(Suppl 48):332S–335S.
Reade, M. C., and J. D. Young. 2003. Of mice and men (and rats): implications of species and stimulus differences for the interpretation of studies of nitric oxide in sepsis. Br. J. Anaesth. 90:115–118.
Canada, A. T., E. J. Calabrese, and D. Leonard. 1986. Age-dependent inhibition of pentobarbital sleeping time by ozone in mice and rats. J. Gerontol. 41:587–589.
Rilling, S., and R. Viebahn. 1990. Praxis der Ozon-Sauerstoff-Therapie, E. Fischer ed., Verlag fur Medizin, Heidelberg.
Hatch, G., R. Slade, L. Harris, W. McDonnel, R. Devlin, H. Koren, D. Costa, and J. McKee. 1994. Ozone dose and effect in humans and rats. A comparison using oxygen-18 labeling and bronchoalveolar lavage. Am. J. Respir. Crit. Care Med. 150:676–683.
Korbut, R., and J. Gryglewski. 1996. The effect of prostacyclin and nitric oxide on deformability of red blood cells in septic shock in rats. J. Physiol. Pharmacol. 47:591–599.
Jimba, M., W. Skornik, C. Killinsworth, N. Long, J. Brain, and S. Shore. 1995. Role of C fibers in physiological responses to ozone in rats. J. Appl. Physiol. 78:1757–1763.
Verrazzo, G., L. Coppola, C. Luongo, A. Sammartino, R. Giunta, A. Grassia, R. Ragone, and A. Tirelli. 1995. Hyperbaric oxygen, oxygen-ozone therapy, and rheologic parameters of blood in patients with peripheral occlusive arterial disease. Undersea Hyperb. Med. 22:17–22.
Young, C., and D. K. Bhalla. 1995. Effects of ozone on the epithelial and inflammatory responses in the airways: role of tumor necrosis factor. J. Toxicol. Environ. Health 46:329–342.
Wielgus-Serafińska, E., A. Plewka, and M. Kamiński. 1993.Circadian variation of mitochondrial succinic dehydrogenase and microsomal cytochrome P-450 dependent monooxygenase activity in the liver of sexually immature and mature rats. J. Physiol. Pharmacol. 44:55–63.
Czekaj, P., A. Plewka, M. Kamiński, G. Nowaczyk, K. Pawlicki, and E. Wielgus-Serafińska. 1994. Daily and circadian rhythms in the activity of mixed function oxidases system in rats of different age. Biol. Rhythm. Res. 25:67–75.
Misra, H. P., and I. Fridovich. 1972. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J. Biol. Chem. 247:3170–3175.
Aebi, M. 1974. Catalase, methods of enzymatic analysis. In: H. Bermeyer ed., Academic Press, NY, pp. 674–678.
Madej, J. A., C. Kaszubkiewicz, M. Mazurkiewicz, S. Klientowski, and L. Fiszer. 1983. Test of usage chemiluminescence in diagnosis of lymphatic leukaemia P388 in mice. Med. Wet. 39:682–685.
Niwa, Y. 1989. Lipid peroxides and superoxide dismutase (SOD) induction in skin inflammatory diseases, and treatment with SOD preparations. Dermatologica 179(Suppl 1):101–106.
Iizawa, O., T. Kato, H. Tagami, and Y. Niwa. 1991. Lipid peroxides and superoxide dismutase activity in trichophyte lesions. Arch. Dermatol. 127:1241–1243.
Gregory, E. M., S. A. Goscin, and I. Fridovich. 1974. Superoxide dismutase and oxygen toxicity in a eukaryote. J. Bacteriol. 117:456–460.
Archibald, F. 2003. Oxygen toxicity and the health and survival of eukaryote cells: a new piece is added to the puzzle. Proc. Natl. Acad. Sci. U.S.A. 100:10141–10143.
Aruoma, O. I., B. Halliwell, and M. Dizdaroglu. 1989. Iron ion-dependent modification of bases in DNA by the superoxide radical-generating system hypoxanthine/xanthine oxidase. J. Biol. Chem. 264:13024–13028.
Takehara, Y., K. Yamaoka, E. F. Sato, T. Yoshioka, and K. Utsumi. 1994. DNA damage by various forms of active oxygens and its inhibition by different scavengers using plasmid DNA. Physiol. Chem. Phys. Med. NMR 26:215–226.
Wolff, S. P., and R. T. Dean. 1986. Fragmentation of proteins by free radicals and its effect on their susceptibility to enzymic hydrolysis. Biochem. J. 234:399–403.
Davies, K. J. 1987. Protein damage and degradation by oxygen radicals. I. general aspects. J. Biol. Chem. 262:9895–9901.
Halliwell, B., and J. M. Gutteridge. 1988. Free radicals and antioxidant protection: mechanisms and significance in toxicology and disease. Human Toxicol. 7:7–13.
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Madej, P., Plewka, A., Madej, J.A. et al. Ozonotherapy in an Induced Septic Shock. I. Effect of Ozonotherapy on Rat Organs in Evaluation of Free Radical Reactions and Selected Enzymatic Systems. Inflammation 30, 52–58 (2007). https://doi.org/10.1007/s10753-007-9021-7
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DOI: https://doi.org/10.1007/s10753-007-9021-7