Mechanism of Action of Ozone in the Treatment of Non-Healing Ulcers:
- Improves Blood Circulation and Tissue Oxygenation:
- Increases oxygen release at the tissue level by elevating 2,3 DPG.
- Induces vasodilation by generating Nitric Oxide.
- Raises ATP levels, influencing membrane potential and enhancing the deformability and elasticity of red blood cells (RBCs).
- Stimulates Immune System and Pathogen Elimination:
- Modulates cell-mediated immunity, controlling cytokines like IL, IL2, IL-12, INFY, and TNFO.
- Regulates humoral immunity through IL4, IL5, IL-10, and TGFB.
- Affects leucocytes, particularly Helper T Lymphocytes, by modifying cytokine synthesis, influencing pro-inflammatory/anti-inflammatory cytokines like IL-6, IL-4, TNFO, IFN-B, IFNY, IL-2, and IL-10.
- Platelets Activation and Growth Factor Release:
- Stimulates platelets to produce PDGF (Platelet-Derived Growth Factor), promoting fibroblast proliferation and extracellular matrix production.
- Releases chemotactic factors like TGFB (Tumor Growth Factor B) and IL8 (Interleukin 8), fostering collagen deposition, matrix formation, and angiogenesis.
- Germicidal Ozone Properties:
- Exhibits potent bactericidal, fungicidal, and virucidal properties, commonly employed for disinfecting infected wounds.
- Alters bacterial cell membrane structure by attacking PUFA, leading to increased porosity, cell damage, rupture, and death.
- Activates macrophages and T cells, promoting phagocytosis and antibody production to effectively combat bacteria.
- Blocks viral replication through the ozone-induced synthesis of IFN (Interferon).
- Displays efficacy against fungi, particularly in higher concentrations.
- Enhances and Activates Body’s Own Antioxidants:
- Despite its oxidant nature, ozone stimulates the body’s antioxidant enzymes such as glutathione, peroxidase, catalase, and superoxide dismutase.
- Prepares the body for subsequent oxidative stress by enhancing its antioxidant defenses.