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NADPH oxidase 4 and its role in the cardiovascular system

The heart relies on complex mechanisms that provide adequate myocardial oxygen supply in order to maintain its contractile function. At the cellular level, oxygen undergoes one electron reduction to superoxide through the action of different types of oxidases (e.g. xanthine oxidases, uncoupled nitri...

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Detalles Bibliográficos
Autores principales: Gray, Stephen P, Shah, Ajay M, Smyrnias, Ioannis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439918/
https://www.ncbi.nlm.nih.gov/pubmed/32923955
http://dx.doi.org/10.1530/VB-19-0014
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author Gray, Stephen P
Shah, Ajay M
Smyrnias, Ioannis
author_facet Gray, Stephen P
Shah, Ajay M
Smyrnias, Ioannis
author_sort Gray, Stephen P
collection PubMed
description The heart relies on complex mechanisms that provide adequate myocardial oxygen supply in order to maintain its contractile function. At the cellular level, oxygen undergoes one electron reduction to superoxide through the action of different types of oxidases (e.g. xanthine oxidases, uncoupled nitric oxide synthases, NADPH oxidases or NOX). Locally generated oxygen-derived reactive species (ROS) are involved in various signaling pathways including cardiac adaptation to different types of physiological and pathophysiological stresses (e.g. hypoxia or overload). The specific effects of ROS and their regulation by oxidases are dependent on the amount of ROS generated and their specific subcellular localization. The NOX family of NADPH oxidases is a main source of ROS in the heart. Seven distinct Nox isoforms (NOX1–NOX5 and DUOX1 and 2) have been identified, of which NOX1, 2, 4 and 5 have been characterized in the cardiovascular system. For the purposes of this review, we will focus on the effects of NADPH oxidase 4 (NOX4) in the heart.
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spelling pubmed-74399182020-09-10 NADPH oxidase 4 and its role in the cardiovascular system Gray, Stephen P Shah, Ajay M Smyrnias, Ioannis Vasc Biol Mini Review The heart relies on complex mechanisms that provide adequate myocardial oxygen supply in order to maintain its contractile function. At the cellular level, oxygen undergoes one electron reduction to superoxide through the action of different types of oxidases (e.g. xanthine oxidases, uncoupled nitric oxide synthases, NADPH oxidases or NOX). Locally generated oxygen-derived reactive species (ROS) are involved in various signaling pathways including cardiac adaptation to different types of physiological and pathophysiological stresses (e.g. hypoxia or overload). The specific effects of ROS and their regulation by oxidases are dependent on the amount of ROS generated and their specific subcellular localization. The NOX family of NADPH oxidases is a main source of ROS in the heart. Seven distinct Nox isoforms (NOX1–NOX5 and DUOX1 and 2) have been identified, of which NOX1, 2, 4 and 5 have been characterized in the cardiovascular system. For the purposes of this review, we will focus on the effects of NADPH oxidase 4 (NOX4) in the heart. Bioscientifica Ltd 2019-07-11 /pmc/articles/PMC7439918/ /pubmed/32923955 http://dx.doi.org/10.1530/VB-19-0014 Text en © 2019 The authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Mini Review
Gray, Stephen P
Shah, Ajay M
Smyrnias, Ioannis
NADPH oxidase 4 and its role in the cardiovascular system
title NADPH oxidase 4 and its role in the cardiovascular system
title_full NADPH oxidase 4 and its role in the cardiovascular system
title_fullStr NADPH oxidase 4 and its role in the cardiovascular system
title_full_unstemmed NADPH oxidase 4 and its role in the cardiovascular system
title_short NADPH oxidase 4 and its role in the cardiovascular system
title_sort nadph oxidase 4 and its role in the cardiovascular system
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439918/
https://www.ncbi.nlm.nih.gov/pubmed/32923955
http://dx.doi.org/10.1530/VB-19-0014
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