Susceptibility of Glutathione Peroxidase and Glutathione Reductase to Oxidative Damage and the Protective Effect of Spin Trapping Agents

• Published in: Archives of biochemistry and biophysics Vol. 314; no. 1; pp. 112 - 119
• Main Authors: Tabatabaie, T., Floyd, R.A.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.10.1994
• Subjects: Animals; Ascorbic Acid - pharmacology; Cattle; Chromatography, High Pressure Liquid; CONTAMINANTES; Cyclic N-Oxides - pharmacology; DESINFECTANT; DESINFECTANTES; Erythrocytes - enzymology; ESTRES; FER; Ferric Compounds - pharmacology; Ferrous Compounds - pharmacology; GLUTATHION PEROXYDASE; Glutathione Peroxidase - metabolism; Glutathione Reductase - metabolism; GLUTATION PEROXIDASA; HIERRO; Hydroxyl Radical - metabolism; Light; Methylene Blue - pharmacology; Nitrogen Oxides - pharmacology; OXIDACION; Oxidation-Reduction; OXYDATION; Oxygen - metabolism; OZONE; Ozone - pharmacology; OZONO; PEROXIDO DE HIDROGENO; PEROXYDE D'HYDROGENE; POLLUANT; PRODUCTOS QUIMICOS; PRODUIT CHIMIQUE; RADIACION ULTRAVIOLETA; RAYONNEMENT ULTRAVIOLET; Singlet Oxygen; Spin Labels; STRESS
• ISSN: 0003-9861; 1096-0384
• DOI: 10.1006/abbi.1994.1418

Susceptibility of two key protective enzymes, glutathione peroxidase (GPX) and glutathione reductase (GR), to oxidative damage and the possible protective action of spin traps have been studied. Several oxidizing protocols including: (a) Fe(II) or Fe(III)/ascorbate, (b) a singlet oxygen producing system (methylene blue and visible light), (c) ozone, and (d) a hydroxyl radical-generating system (hydrogen peroxide/uv light) have been employed. Our results show that both enzymes are susceptible to oxidative modification and damage as indicated by the loss of activity and formation of carbonyl groups (in the case of GR). Treatment of GR with any of the mentioned oxidants resulted in formation of carbonyl groups and inactivation except when treated with iron, where the observed carbonyl formation was not accompanied with significant activity loss. GPX was inactivated to varying degrees when treated with the mentioned oxidants, but no carbonyls were detected. Ultraviolet exposure per se resulted in inactivation of both enzymes. Presence of the spin traps N-tert-butyl-α-phenylnitrone or 5,5′-dimethyl-1-pyroline- N-oxide was effective in protecting the enzymes against oxidation by uv, hydrogen peroxide/uv, and ozone as determined by the preservation of activity and decreased carbonyl content. The degree of protection, however, was found to be specific for each enzyme and for the employed oxidizing system.