Peroxynitrous acid synthesized by reaction of hydrogen peroxide and nitrite
and generated from 3-morpholinosydononimine (SIN-1) induced cellular DNA b
reaking of human promyelocytic leukemia HL-60 cells in phosphate buffer (pH
7.5) as assessed by alkaline single cell gel electrophoresis (comet) assay
and quantification of comet types. Ascorbate and Trolox inhibited cellular
DNA breaking induced by peroxynitrous acid, but the concentrations of thes
e antioxidants required for effective inhibition was about 50-fold higher t
han that of peroxynitrous acid. beta-Carotene protected DNA breaking by per
oxynitrous acid in 20% tetrahydrofuran-phosphate buffer (pH 7.5) much more
effectively than ascorbate and Trolox. The concentrations of beta-carotene
required for effective inhibition was lower than the concentration of perox
ynitrous acid.