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. 2007 Apr;30(1-2):52-8.
doi: 10.1007/s10753-007-9021-7. Epub 2007 Feb 14.

Ozonotherapy in an induced septic shock. I. Effect of ozonotherapy on rat organs in evaluation of free radical reactions and selected enzymatic systems

Affiliations

Ozonotherapy in an induced septic shock. I. Effect of ozonotherapy on rat organs in evaluation of free radical reactions and selected enzymatic systems

Pawel Madej et al. Inflammation. 2007 Apr.

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 O(2)/O(3) (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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References

    1. J Physiol Pharmacol. 1996 Dec;47(4):591-9 - PubMed
    1. Mediators Inflamm. 1998;7(4):289-94 - PubMed
    1. Clin Pharm. 1992 Mar;11(3):223-35 - PubMed
    1. Br J Anaesth. 2003 Feb;90(2):115-8 - PubMed
    1. J Bacteriol. 1974 Feb;117(2):456-60 - PubMed

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