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Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease?

Peripheral Arterial Disease (PAD) is a cause of significant morbidity and mortality in the Western world. Risk factor modification and endovascular and surgical revascularisation are the main treatment options at present. However, a significant number of patients still require major amputation. Ther...

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Autores principales: Williams, Gareth, Shi-Wen, Xu, Abraham, David, Selvakumar, Sadasivam, Baker, Daryll M., Tsui, Janice C. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3318888/
https://www.ncbi.nlm.nih.gov/pubmed/22536531
http://dx.doi.org/10.1155/2012/656247
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author Williams, Gareth
Shi-Wen, Xu
Abraham, David
Selvakumar, Sadasivam
Baker, Daryll M.
Tsui, Janice C. S.
author_facet Williams, Gareth
Shi-Wen, Xu
Abraham, David
Selvakumar, Sadasivam
Baker, Daryll M.
Tsui, Janice C. S.
author_sort Williams, Gareth
collection PubMed
description Peripheral Arterial Disease (PAD) is a cause of significant morbidity and mortality in the Western world. Risk factor modification and endovascular and surgical revascularisation are the main treatment options at present. However, a significant number of patients still require major amputation. There is evidence that nitric oxide (NO) and its endogenous inhibitor asymmetric dimethylarginine (ADMA) play significant roles in the pathophysiology of PAD. This paper reviews experimental work implicating the ADMA-DDAH-NO pathway in PAD, focussing on both the vascular dysfunction and effects within the ischaemic muscle, and examines the potential of manipulating this pathway as a novel adjunct therapy in PAD.
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spelling pubmed-33188882012-04-25 Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease? Williams, Gareth Shi-Wen, Xu Abraham, David Selvakumar, Sadasivam Baker, Daryll M. Tsui, Janice C. S. Cardiol Res Pract Review Article Peripheral Arterial Disease (PAD) is a cause of significant morbidity and mortality in the Western world. Risk factor modification and endovascular and surgical revascularisation are the main treatment options at present. However, a significant number of patients still require major amputation. There is evidence that nitric oxide (NO) and its endogenous inhibitor asymmetric dimethylarginine (ADMA) play significant roles in the pathophysiology of PAD. This paper reviews experimental work implicating the ADMA-DDAH-NO pathway in PAD, focussing on both the vascular dysfunction and effects within the ischaemic muscle, and examines the potential of manipulating this pathway as a novel adjunct therapy in PAD. Hindawi Publishing Corporation 2012 2012-03-20 /pmc/articles/PMC3318888/ /pubmed/22536531 http://dx.doi.org/10.1155/2012/656247 Text en Copyright © 2012 Gareth Williams et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Williams, Gareth
Shi-Wen, Xu
Abraham, David
Selvakumar, Sadasivam
Baker, Daryll M.
Tsui, Janice C. S.
Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease?
title Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease?
title_full Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease?
title_fullStr Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease?
title_full_unstemmed Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease?
title_short Nitric Oxide Manipulation: A Therapeutic Target for Peripheral Arterial Disease?
title_sort nitric oxide manipulation: a therapeutic target for peripheral arterial disease?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3318888/
https://www.ncbi.nlm.nih.gov/pubmed/22536531
http://dx.doi.org/10.1155/2012/656247
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