Indirect Antioxidant Effects of the Nitrite Anion: Focus on Xanthine Oxidase

• Published in: Advances in redox research : an official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe Vol. 7; p. 100058
• Main Authors: Williams, Xena M., Bossert, Alec T., Devalance, Evan, Lewis, Sara E., Gunther, Michael R., Kelley, Eric E.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.04.2023; Elsevier
• Subjects: nitric oxide; nitrite; oxidants, nitrite, nitrate; xanthine oxidoreductase; NO; xanthine oxidoreductase; nitric oxide; O2; oxidants, nitrite, nitrate; SOD; H2O2; NO2; nitrite; NOS; NO3; XO; XOR; XDH; oxidants; nitrate
• ISSN: 2667-1379; 2667-1379
• DOI: 10.1016/j.arres.2022.100058

•Under hypoxia, nitrite inhibits O2●− and H2O2 generation by XO and xanthine.•Nitrate does not alter oxidant generation from XO and xanthine when O2 is present.•Both nitrite and nitrate diminish XO-dependent H2O2 generation in liver tissue.•Nitrate may alter capacity for nitrite to diminish XO-catalyzed oxidant formation. One electron reduction of nitrite (NO2−) has been determined to be a significant, noncanonical source of nitric oxide (NO) with molybdopterin enzymes being identified as critical to this process. Of the molybdopterin enzymes identified as NO2− reductases, xanthine oxidoreductase (XOR) is the most extensively studied. Paradoxically, XOR generates oxidants and thus can contribute to oxidative stress under inflammatory conditions when the oxidase form (XO) of XOR is abundant. However, under similar inflammatory conditions XO has been associated with NO generation, especially when NO2− levels are elevated which begs the question: if reaction of nitrite with XO consumes electrons, then does it subsequently reduce oxidant generation? To address this question, electron paramagnetic resonance (EPR) was used, under controlled O2 tensions, to assess superoxide (O2·−) generation by endothelial-bound XO plus xanthine and the resultant impact of introducing NO2−. Nitrite diminished XO-derived O2·− under hypoxia (1% O2) whereas at 21% O2, it had no impact. To confirm these results and discount contributions from the reaction of NO with O2·−, molecular O2 consumption was assessed. The presence of NO2− decreased the rate of XO/xanthine-dependent O2 consumption in a concentration-dependent manner with greater impact under hypoxic conditions (1% O2) compared to 21% O2. In a more biologic setting, NO2− also diminished XO-dependent H2O2 formation in murine liver homogenates supplemented with xanthine. Interestingly, nitrate (NO3−) did not alter XO-dependent O2 consumption at either 21% or 1% O2; yet it did slightly impact nitrite-mediated effects when present at 2:1 ratio vs. NO2−. When combined, these data: 1) show a significant indirect antioxidant function for NO2− by decreasing oxidant generation from XO, 2) demonstrate that both XO-derived H2O2 and O2·− production are diminished by the presence of NO2− and 3) incentivize further exploration of the difference between XO reaction with NO2− vs. NO3−.