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NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies
NADPH oxidase family enzymes (or NOXs) are the major sources of reactive oxygen species (ROS) that are implicated in the pathophysiology of many cardiovascular diseases. These enzymes appear to be especially important in the modulation of redox-sensitive signalling pathways that underlie key cellula...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149671/ https://www.ncbi.nlm.nih.gov/pubmed/21598086 http://dx.doi.org/10.1007/s00395-011-0190-z |
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author | Sirker, Alexander Zhang, Min Shah, Ajay M. |
author_facet | Sirker, Alexander Zhang, Min Shah, Ajay M. |
author_sort | Sirker, Alexander |
collection | PubMed |
description | NADPH oxidase family enzymes (or NOXs) are the major sources of reactive oxygen species (ROS) that are implicated in the pathophysiology of many cardiovascular diseases. These enzymes appear to be especially important in the modulation of redox-sensitive signalling pathways that underlie key cellular functions such as growth, differentiation, migration and proliferation. Seven distinct members of the family have been identified of which four (namely NOX1, 2, 4 and 5) may have cardiovascular functions. In this article, we review our current understanding of the roles of NOX enzymes in several common cardiovascular disease states, with a focus on data from genetic studies and clinical data where available. |
format | Online Article Text |
id | pubmed-3149671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-31496712011-09-08 NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies Sirker, Alexander Zhang, Min Shah, Ajay M. Basic Res Cardiol Invited Review NADPH oxidase family enzymes (or NOXs) are the major sources of reactive oxygen species (ROS) that are implicated in the pathophysiology of many cardiovascular diseases. These enzymes appear to be especially important in the modulation of redox-sensitive signalling pathways that underlie key cellular functions such as growth, differentiation, migration and proliferation. Seven distinct members of the family have been identified of which four (namely NOX1, 2, 4 and 5) may have cardiovascular functions. In this article, we review our current understanding of the roles of NOX enzymes in several common cardiovascular disease states, with a focus on data from genetic studies and clinical data where available. Springer-Verlag 2011-05-20 2011 /pmc/articles/PMC3149671/ /pubmed/21598086 http://dx.doi.org/10.1007/s00395-011-0190-z Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Invited Review Sirker, Alexander Zhang, Min Shah, Ajay M. NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies |
title | NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies |
title_full | NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies |
title_fullStr | NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies |
title_full_unstemmed | NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies |
title_short | NADPH oxidases in cardiovascular disease: insights from in vivo models and clinical studies |
title_sort | nadph oxidases in cardiovascular disease: insights from in vivo models and clinical studies |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149671/ https://www.ncbi.nlm.nih.gov/pubmed/21598086 http://dx.doi.org/10.1007/s00395-011-0190-z |
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