Skip to main content
. 2015 Mar;352(3):529–540. doi: 10.1124/jpet.114.221572

Fig. 4.

Fig. 4.

Effects of sulfa drugs on enzymes known to mediate chemical redox cycling. Human sepiapterin reductase (hSPR; 60 nM), human cytochrome P450 reductase (hOR; 1 nM), rat cytosolic TrxR (rTrxR1; 30 nM), or human glutathione reductase (hGR; 70 nM) was incubated in 50 mM potassium phosphate buffer (pH 7.8) with menadione (MD; 200 μM) in the absence or presence of sulfasalazine (SSZ; 100 μM) or sulfamethoxazole (SMX; 100 μM). The reactions were initiated by the addition of NADPH (200 μM) and H2O2 production was measured by the Amplex Red assay. Data are presented as percentage of activity of control enzyme reactions run in the absence of inhibitors. Data are the mean ± S.E. (n = 3). *Significantly different (P < 0.05) from menadione-treated samples in the absence of inhibitors.