Microassay of superoxide anion scavenging activity in vitro

DW Laight, TJ Andrews, AI Haj-Yehia… - Environmental …, 1997 - Elsevier
DW Laight, TJ Andrews, AI Haj-Yehia, MJ Carrier, EE Änggård
Environmental Toxicology and Pharmacology, 1997Elsevier
We have developed a photometric, platereader-based microassay for superoxide anion
scavening activity in vitro. Superoxide anions were generated using a xanthine
oxidase/hypoxanthine system and detected by following the reduction of ferricytochrome c at
550 nM. Inhibitory activity was assessed for superoxide dismutase (SOD) and the
superoxide anion scavengers tiron and TEMPO together with a number of TEMPO
derivatives. The initial rate of change in optical density (OD) at 550 nm, ie, initial reaction …
We have developed a photometric, platereader-based microassay for superoxide anion scavening activity in vitro. Superoxide anions were generated using a xanthine oxidase/hypoxanthine system and detected by following the reduction of ferricytochrome c at 550 nM. Inhibitory activity was assessed for superoxide dismutase (SOD) and the superoxide anion scavengers tiron and TEMPO together with a number of TEMPO derivatives. The initial rate of change in optical density (OD) at 550 nm, i.e., initial reaction rate, generated by xanthine oxidase (20 mU/ml)/hypoxanthine (100 μM) coupled to ferricytochrome c (100 μM) was effectively abolished by SOD (200 U/ml), tiron (10 mM) and TEMPO (0.3 mM), indicating the involvement of superoxide anions. TEMPO derivatives inhibited the initial reaction rate with the potency order: TEMPO > 4-hydroxy-TEMPO = 4-carboxy-TEMPO. In contrast, 4-hydroxy-TEMPO, which lacks the free radical nitroxide function, was inactive up to 1 mM.
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