Xanthine oxidoreductase: A leading actor in cardiovascular disease drama

Cardiovascular diseases (CVD) are the leading cause of global mortality and their pathogenesis lies mainly in the atherosclerotic process. There are close connections linking oxidative stress and inflammation to endothelial dysfunction, atherosclerosis and, consequently, to CVD. This review focuses...

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Autores principales: Letizia Polito, Massimo Bortolotti, Maria Giulia Battelli, Andrea Bolognesi
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/4408fe5b6fd343a3bd633492cf7eaf98
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spelling oai:doaj.org-article:4408fe5b6fd343a3bd633492cf7eaf982021-11-28T04:31:25ZXanthine oxidoreductase: A leading actor in cardiovascular disease drama2213-231710.1016/j.redox.2021.102195https://doaj.org/article/4408fe5b6fd343a3bd633492cf7eaf982021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2213231721003554https://doaj.org/toc/2213-2317Cardiovascular diseases (CVD) are the leading cause of global mortality and their pathogenesis lies mainly in the atherosclerotic process. There are close connections linking oxidative stress and inflammation to endothelial dysfunction, atherosclerosis and, consequently, to CVD. This review focuses on the role of xanthine oxidoreductase (XOR) and its products on the development of chronic inflammation and oxidative stress, responsible for atheromatous plaque formation. Evidence is reported that an excessive level of XOR products favors inflammatory response and plaque development, thereby promoting major cardiovascular risk factors. Also, the relationship between hyperuricemia and hypertension as well as between XOR activity and CVD is confirmed. In spite of the increasing number of clinical studies investigating the output of cardiovascular patients treated with urate-lowering therapies (including uricosuric drugs, XOR inhibitors and recombinant uricase) the results are still uncertain. The inhibition of XOR activity appears more promising than just the control of uricemia level in preventing cardiovascular events, possibly because it also reduces the intracellular accumulation of urate, as well as the production of reactive oxygen species. However, XOR inhibition also reduces the availability of the multifaced mediator nitric oxide and, at present, can be recommended only in hyperuricemic patients.Letizia PolitoMassimo BortolottiMaria Giulia BattelliAndrea BolognesiElsevierarticleAtherosclerosisCardiovascular diseasesHypertensionNitric oxideReactive oxygen speciesUric acidMedicine (General)R5-920Biology (General)QH301-705.5ENRedox Biology, Vol 48, Iss , Pp 102195- (2021)
institution DOAJ
collection DOAJ
language EN
topic Atherosclerosis
Cardiovascular diseases
Hypertension
Nitric oxide
Reactive oxygen species
Uric acid
Medicine (General)
R5-920
Biology (General)
QH301-705.5
spellingShingle Atherosclerosis
Cardiovascular diseases
Hypertension
Nitric oxide
Reactive oxygen species
Uric acid
Medicine (General)
R5-920
Biology (General)
QH301-705.5
Letizia Polito
Massimo Bortolotti
Maria Giulia Battelli
Andrea Bolognesi
Xanthine oxidoreductase: A leading actor in cardiovascular disease drama
description Cardiovascular diseases (CVD) are the leading cause of global mortality and their pathogenesis lies mainly in the atherosclerotic process. There are close connections linking oxidative stress and inflammation to endothelial dysfunction, atherosclerosis and, consequently, to CVD. This review focuses on the role of xanthine oxidoreductase (XOR) and its products on the development of chronic inflammation and oxidative stress, responsible for atheromatous plaque formation. Evidence is reported that an excessive level of XOR products favors inflammatory response and plaque development, thereby promoting major cardiovascular risk factors. Also, the relationship between hyperuricemia and hypertension as well as between XOR activity and CVD is confirmed. In spite of the increasing number of clinical studies investigating the output of cardiovascular patients treated with urate-lowering therapies (including uricosuric drugs, XOR inhibitors and recombinant uricase) the results are still uncertain. The inhibition of XOR activity appears more promising than just the control of uricemia level in preventing cardiovascular events, possibly because it also reduces the intracellular accumulation of urate, as well as the production of reactive oxygen species. However, XOR inhibition also reduces the availability of the multifaced mediator nitric oxide and, at present, can be recommended only in hyperuricemic patients.
format article
author Letizia Polito
Massimo Bortolotti
Maria Giulia Battelli
Andrea Bolognesi
author_facet Letizia Polito
Massimo Bortolotti
Maria Giulia Battelli
Andrea Bolognesi
author_sort Letizia Polito
title Xanthine oxidoreductase: A leading actor in cardiovascular disease drama
title_short Xanthine oxidoreductase: A leading actor in cardiovascular disease drama
title_full Xanthine oxidoreductase: A leading actor in cardiovascular disease drama
title_fullStr Xanthine oxidoreductase: A leading actor in cardiovascular disease drama
title_full_unstemmed Xanthine oxidoreductase: A leading actor in cardiovascular disease drama
title_sort xanthine oxidoreductase: a leading actor in cardiovascular disease drama
publisher Elsevier
publishDate 2021
url https://doaj.org/article/4408fe5b6fd343a3bd633492cf7eaf98
work_keys_str_mv AT letiziapolito xanthineoxidoreductasealeadingactorincardiovasculardiseasedrama
AT massimobortolotti xanthineoxidoreductasealeadingactorincardiovasculardiseasedrama
AT mariagiuliabattelli xanthineoxidoreductasealeadingactorincardiovasculardiseasedrama
AT andreabolognesi xanthineoxidoreductasealeadingactorincardiovasculardiseasedrama
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