Xanthine oxidoreductase: One enzyme for multiple physiological tasks.
Nitric oxide
Reactive oxygen species
Uric acid
Xanthine oxidoreductase
Journal
Redox biology
ISSN: 2213-2317
Titre abrégé: Redox Biol
Pays: Netherlands
ID NLM: 101605639
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
received:
19
11
2020
revised:
22
01
2021
accepted:
24
01
2021
pubmed:
13
2
2021
medline:
6
7
2021
entrez:
12
2
2021
Statut:
ppublish
Résumé
Human xanthine oxidoreductase (XOR) is a multiple-level regulated enzyme, resulting from a complicated evolutionary process that assigned it many physiological roles. The main XOR activities are: (i) xanthine dehydrogenase (XDH) activity that performs the last two steps of purine catabolism, from hypoxanthine to uric acid; (ii) xanthine oxidase (XO) activity that, besides purine catabolism, produces reactive oxygen species (ROS); (iii) nitrite reductase activity that generates nitric oxide, contributing to vasodilation and regulation of blood pressure; (iv) NADH oxidase activity that produces ROS. All these XOR activities contribute also to metabolize various endogenous and exogenous compounds, including some drugs. About XOR products, it should be considered that (i) uric acid is not only a proinflammatory agent, but also a fundamental antioxidant molecule in serum and (ii) XOR-derived ROS are essential to the inflammatory defensive response. Although XOR has been the object of a large number of studies, most of them were focused on the pathological consequences of its activity and there is not a clear and schematic picture of XOR physiological roles. In this review, we try to fill this gap, reporting and graphically schematizing the main roles of XOR and its products.
Identifiants
pubmed: 33578127
pii: S2213-2317(21)00030-6
doi: 10.1016/j.redox.2021.101882
pmc: PMC7879036
pii:
doi:
Substances chimiques
Reactive Oxygen Species
0
Uric Acid
268B43MJ25
Nitric Oxide
31C4KY9ESH
Xanthine Dehydrogenase
EC 1.17.1.4
Xanthine Oxidase
EC 1.17.3.2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
101882Informations de copyright
Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.