Ozone Therapy
PHYSIOCHEMICAL PROPERTIES of Gaziantep ozone therapy
Gaziantep Ozone Therapy; Ozone is the third most powerful known on earth. OXIDANT AGENT due to being THE MOST POWERFUL NATURAL DISINFECTANT It is considered. It is considered to be 3125 times more potent germicidal than Chlorine, a widely used disinfectant.
O3, the third strongest oxidant; I. Oxidizing Agent ; fluorine
II. Oxidant Agent ; persulphate III. Oxidizing Agent ; Ozone-O3
(Bocci V. Scientific and medical aspects of ozone therapy. state of the
art. Archives of Medical Research. 2006;37:425–435).
Gaziantep Effect Mechanism of Ozone Therapy
The most important effect of ozoneEXOGENE ACUTE OXIDATIVE STRESS by creating ACTIVATING ANTIOXIDANT SYSTEM (AOS Enzymes: Glutathione By increasing peroxidase, catalase, superoxide dismutase enzyme activation) ACTIVATING and where AOS is strong and stable; MİTOKONDRİ (ATP yapını arttırmak), IMMUNE SYSTEM, DETOXIFICATION AND METABOLIC-HORMONAL SYSTEMS considered to work better.
Since microorganisms have weaker AOS compared to healthy cells, microorganisms are more sensitive to ozone, that is, they are more affected. Since the antioxidant systems of microorganisms are insufficient against the strong oxidative stress created by ozone, the m.o s are disintegrating.
Since ozone decomposes microorganisms (Bacteria, Viruses, Fungi and Protozoa) by oxidizing phospholipids and lipoproteins, viruses containing lipid-rich envelopes are more sensitive to ozone. Ozone disrupts the virus-cell contact with peroxidation, damaging the viral capsid and interrupting the reproductive cycle. Fungi also inhibit cell proliferation at certain stages (V. Bocci, Italy and R. Viebahn, Germany).
Viruses containing lipid envelopes (such as Herpes, HCV, HIV) that can be easily oxidized by O3 are more sensitive to ozone. Enveloped viruses with higher lipid content are more sensitive to ozone than non-enveloped viruses since they contain more lipid that interacts easily with O3 (Italy-V .Bocci, Cuba-B.I. Sofronov et al., 1995).
O3 INCREASES THE PRODUCTION OF LEUCOCYTE. Since leukocytes have low antioxidant enzyme (GSH) levels, they are not protected against ROS formed during phagocytosis.(Deforge et al.1992, Anderson et al.1996, Sen and Packer.1996, Flohe and Suzuki et al.1997, Ginn- Peas and Wishler.1998,
MODULATES CYTOKINE RELEASE of Gaziantep ozone therapy.
Denaturation of virions by direct contact with ozone. Ozone degrades viral envelope proteins, lipoproteins, lipids and glycoproteins. The large number of double bonds in these unsaturated molecules makes them vulnerable to the oxidizing effects of ozone.
interferons (IFN-a, IFN-b, and IFN-g), Interleukins (interleukins of the types IL-1b, 2, 4, 6, 8, 10), Tumor Necrosis Factor (TNF – a), Granulocyte Macrophage Colony Stimulant It has been shown to increase the release of Factor (GM-CSF) and Transforming Growth Factor (TGF-β1).It has been shown that ozone at appropriate doses can induce the release of interferon γ (IFN-γ) in human blood. Results were obtained by ozonation of blood directly, detection of cytokines in plasma during 4-8 hour incubations. Various findings have been expressed, such as the protective effect of blood antioxidants, increased ozone concentrations of different cytokines, especially decreased cytokine activity above 80 μg/ml per ml of blood. (Bocci et al 1990 &1993, Paulesu et al 1991, Larini et al 2001).
In addition, some authors (Beck et al., 1994; Arsalane et al., 1995; Jaspers et al., 1997) have confirmed that ozone can induce cytokine production after epithelial cells of the respiratory mucosa come into contact with ozone.
Ozone therapy in Gaziantep REGULATES CIRCULATION in the organism.
Motility of erythrocytes and oxygenation of tissues (by increasing 2.3 DPG level, increased dissolved oxygen in plasma and increased Partial Oxygen Pressure – PO2) in erythrocytes, increasing nutrition and immunity of tissues by vasodilation of vessels, decreasing aggregation of erythrocyte and thrombocyte cells (with membrane oxidation) and tendency to thrombosis and coagulation and has been shown to reduce viral load. Peripheral blood mononuclear cells (lymphocytes and monocytes, PBMC) were isolated from normal blood donors to investigate their viability and the production and type of secreted cytokines after two different ozonation methods. The first is a direct ozonation of PBMC suspended in human serum so that cells are immediately exposed to ozone due to the very short half-life of hydrogen peroxide (H2O2) and other unidentified reactive oxygen species (early ROS) and late effects, rather long half-life. It is provided by lipid oxidative products (LOPs) that have longevity.
The latter examined the effect of ozonated serum 20 minutes prior to addition to PBMC, and therefore ozone activity is expressed only by “late LOPs”.
Ozone acts as a triggering substrate for various blood components such as erythrocytes, lymphocytes, monocytes, polymorphonuclear leukocytes, platelets and plasma components, and clinical improvement is observed directly or indirectly after autohemotherapeutic treatment in chronic viral diseases.
There are no cases where ozone therapy is applied.
1. Treatment of circulatory disorders and geriatrics
2. In difficult-to-heal infected wounds and inflammatory diseases
3. Supplementary or supplementary in cancer treatment
4. Anti-aging (aging back) and revitalization
5. Prevention and treatment in elderly people
6. Ozone therapy in eye diseases
7. Skin fungi and infected skin lesions
8. Intestinal Diseases:
9. Diseases caused by viruses
10. Liver inflammation (Hepatitis A, B, C)
11. Inflammatory and degenerative joint diseases
12. Arthritic/ Rheumatic Conditions – Chronic polyarthritis
13. Strengthens the immune system
14. Cellulite
15. Chronic Fatigue
16. Increasing Performance in Athletes
