Abstract
Temperature-dependent free radical reactions were investigated using nitroxyl radicals as redox probes. Reactions of two types of nitroxyl radicals, TEMPOL (4-hydroxyl-2,2,6,6-tetramethylpiperidineN-oxyl) and carbamoyl-PROXYL (3-carbamoyl-2,2,5,5-tetramethyl-pyrrolidine-N-oxyl), were tested in this paper. Heating a solution containing a nitroxyl radical and a reduced form of glutathione (GSH) caused temperature-dependent decay of electron para-magnetic resonance (EPR) signal of the nitroxyl radical. Heating a solution of the corresponding hydroxylamine form of the nitroxyl radical showed EPR signal recovery. The GSH-dependent reduction of nitroxyl radicals at 70°C was suppressed by antioxidants, spin trapping agents, and/or bubbling N 2 gas, although heating carbamoyl-PROXYL with GSH showed temporarily enhanced signal decay by bubbling N 2 gas. Since SOD could restrict the GSH-dependent EPR signal decay of TEMPOL, O 2•- is related with this reaction. O 2•- was probably generated from dissolved oxygen in the reaction mixture. Oxidation of the hydroxylamines at 70°C was also suppressed by bubbling N 2 gas. Heating a solution of spin trapping agent, DMPO (5,5-dimethyl-1-pyrroline-N- oxide) showed a temperature-dependent increase of the EPR signal of the hydroxyl radical adduct of DMPO. Synthesis of hydroxyl radical adduct of DMPO at 70°C was suppressed by antioxidants and/or bubbling N 2 gas. The results suggested that heating an aqueous solution containing oxygen can generate O 2•-. ©2012 JCBN.
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Matsumoto, K. I., Nyui, M., Kamibayashi, M., Ozawa, T., Nakanishi, I., & Anzai, K. (2012). Temperature-dependent free radical reaction in water. Journal of Clinical Biochemistry and Nutrition, 50(1), 40–46. https://doi.org/10.3164/jcbn.10-145
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