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

One electron reduction of nitrite (NO(2)(−)) 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 NO(2)(−) reductases, xanthine oxidoreductase (XOR) is the...

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Detalles Bibliográficos
Autores principales: Williams, Xena M., Bossert, Alec T., Devalance, Evan, Lewis, Sara E., Gunther, Michael R., Kelley, Eric E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10100591/
https://www.ncbi.nlm.nih.gov/pubmed/37063462
http://dx.doi.org/10.1016/j.arres.2022.100058
Descripción
Sumario:One electron reduction of nitrite (NO(2)(−)) 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 NO(2)(−) 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 NO(2)(−) 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 O(2) tensions, to assess superoxide (O(2)(•−)) generation by endothelial-bound XO plus xanthine and the resultant impact of introducing NO(2)(−). Nitrite diminished XO-derived O(2)(•−) under hypoxia (1% O(2)) whereas at 21% O(2), it had no impact. To confirm these results and discount contributions from the reaction of NO with O(2)(•−), molecular O(2) consumption was assessed. The presence of NO(2)(−) decreased the rate of XO/xanthine-dependent O(2) consumption in a concentration-dependent manner with greater impact under hypoxic conditions (1% O(2)) compared to 21% O(2). In a more biologic setting, NO(2)(−) also diminished XO-dependent H(2)O(2) formation in murine liver homogenates supplemented with xanthine. Interestingly, nitrate (NO(3)(−)) did not alter XO-dependent O(2) consumption at either 21% or 1% O(2); yet it did slightly impact nitrite-mediated effects when present at 2:1 ratio vs. NO(2)(−). When combined, these data: 1) show a significant indirect antioxidant function for NO(2)(−) by decreasing oxidant generation from XO, 2) demonstrate that both XO-derived H(2)O(2) and O(2)(•−) production are diminished by the presence of NO(2)(−) and 3) incentivize further exploration of the difference between XO reaction with NO(2)(−) vs. NO(3)(−).