Kinetic study on ESR signal decay of nitroxyl radicals, potent redox probes for in vivo ESR spectroscopy, caused by reactive oxygen species

• Published in: Biochimica et biophysica acta Vol. 1573; no. 2; pp. 156 - 164
• Main Authors: Takeshita, Keizo, Saito, Keita, Ueda, Jun-ichi, Anzai, Kazunori, Ozawa, Toshihiko
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 14.11.2002
• Subjects: Cysteine; Electron Spin Resonance Spectroscopy - methods; Hydroxyl Radical - chemistry; In vivo ESR spectroscopy; Kinetics; Nitrogen Oxides - chemistry; Nitroxyl radical; Oxidation-Reduction; Reaction rate constant; Reactive oxygen species; Reactive Oxygen Species - chemistry; Spin Labels; Superoxides - chemistry; Reaction rate constant; Reactive oxygen species; Nitroxyl radical; In vivo ESR spectroscopy
• ISSN: 0304-4165; 0006-3002; 1872-8006
• DOI: 10.1016/S0304-4165(02)00420-8

The effect of the chemical structure of nitroxyl spin probes on the rate at which ESR signals are lost in the presence of reactive oxygen species (ROS) was examined. When the spin probes were reacted with either hydroxyl radical ( OH) or superoxide anion radical (O 2 − ) in the presence of cysteine or NADH, the probes lost ESR signal depending on both their ring structure and substituents. Pyrrolidine nitroxyl probes were relatively resistant to the signal decay caused by O 2 − with cysteine/NADH. Signal decay rates for these reactions correlated with reported redox potentials of the nitroxyl/oxoammonium couple of spin probes, suggesting that the signal decay mechanism in both cases involves the oxidation of a nitroxyl group. The apparent rate constants of the reactions between the spin probe and OH and between the spin probe and O 2 − in the presence of cysteine were estimated using mannitol and superoxide dismutase (SOD), respectively, as competitive standards. The rate constants for spin probes and OH were in the order of 10 9 M −1 s −1, much higher than those for the probes and O 2 − in the presence of cysteine (10 3–10 4 M −1 s −1). These basic data are useful for the measurement of OH and O 2 − in living animals by in vivo ESR spectroscopy.