Table 1.
Radical | Reaction | Biology/function | Refs. |
---|---|---|---|
Superoxide O2·− |
O2 + e− → O2·− | Mainly produced by the reaction of O2 with an escaped electron from mitochondria; also produced by xanthine oxidase, lipoxygenase, cyclooxygenase and NADPH dependent oxygenase. | [3, 6, 7] |
Hydrogen peroxide H2O2 |
2O2·− + 2H+ → 2H2O2 + O2 | An intermediate detoxification of O2·− by SOD; comparatively low intrinsic toxicity and biological half-life make H2O2 well suited to act as an intracellular signaling molecule; involved in remodeling the structure of cells and activation of transcription factors. | [8–12] |
Hypochlorous acid HOCl |
H+ + Cl− + H2O2 → HOCl+H2O | Formed by myeloperoxidase reaction of H+, Cl−, and H2O2; can terminate bacterial DNA replication by destroying DNA anchoring at the membrane. | [13] |
Hydroxyl radical HO· |
HOCl+ O2·− → HO·+O2 + Cl− HOCl+ Fe2+ → HO·+Fe3+ + Cl− HOCl+ Cu+ → HO·+Cu2+ + Cl− H2O2+ Fe2+ → HO·+ Fe3+ + OH− H2O2+ Cu+ → HO·+ Cu2+ + OH− H2O2+ O2·− → HO·+O2 + Cl− |
Produced spontaneously by HOCl with O2·− or metal ions; also produced from H2O2 through Fenton reactions. Because of its high reactivity, short half-life and irreversible modification of macromolecules, HO· has high biological toxicity. | [3] [14] |
Nitric oxide NO |
L-arginine+O2+NADPH → L-citrulline+NO+NADP++e− | Synthesized enzymatically by NOS; can function as a free radical scavenger as it has a long half-life compared with O2·− and HO·. At normal physiological concentrations, NO is an intracellular messenger for guanylate cyclase and protein kinases. NO conjugates with GSH. | [2, 15–17] |
Peroxynitrite ONOO− |
NO + O2·− → ONOO− | In cells with high NO cells (e.g. stimulated leukocytes), reaction can be faster than the dismutation of O2·− by SOD, then ONOO− can undergo hemolysis to form HO·. | [2] |
Nitrogen dioxide NO2 |
ONOO− + H+ → HO·+NO2 2NO+ O2 → 2NO2 |
Increased formation of ONOO− can lead to autohomolysis into HO· and NO2; NO2 can also be produced by direct oxidation of NO by O2. | [2, 18] |