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• W1564564343 abstract "Nitric oxide synthase (NOS) is a ubiquitous enzyme that has an oxygenase and reductase activity. NOS reduce electron acceptors, at the reductase domain, by a one electron mechanism that is not inhibited by superoxide dismutase (SOD). One example of this activity is the direct reduction of ferricytochrome c by nNOS. Redox cycling electron acceptors, such as lucigenin and nitro blue tetrazolium (NBT), are reduced by NOS to generate an intermediate radical (EAred). This radical can then be re oxidized to the parent compound by oxygen, and can generate superoxide in the process. Consequently, both NBT and lucigenin will enhance NADPH-dependent superoxide generation in the presence of flavoprotein reductases such as NOS. The artificial generation of superoxide from lucigenin and NBT is a major pitfall in the use of these compounds as superoxide probes. We conclude that the use of ESR spin-trapping techniques, although not free of problems, is a viable technique for the detection and quantification of superoxide in systems containing neuronal nitric oxide synthase (nNOS)." @default.
• W1564564343 created "2016-06-24" @default.
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• W1564564343 date "1999-01-01" @default.
• W1564564343 modified "2023-10-18" @default.
• W1564564343 title "[18] Electron spin resonance spin-trapping detection of superoxide generated by neuronal nitric oxide synthase" @default.
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• W1564564343 doi "https://doi.org/10.1016/s0076-6879(99)01080-0" @default.
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