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Regulation of Hepatic Paraoxonase-1 Expression

Serum paraoxonase-1 (PON1) is a member of the paraoxonases family (PON1, PON2, and PON3). PON1 is synthesized and secreted by the liver, and in circulation it is associated with HDL. PON1 has antioxidative properties, which are associated with the enzyme's capability to decrease oxidative stres...

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Autor principal: Fuhrman, Bianca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324161/
https://www.ncbi.nlm.nih.gov/pubmed/22548179
http://dx.doi.org/10.1155/2012/684010
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author Fuhrman, Bianca
author_facet Fuhrman, Bianca
author_sort Fuhrman, Bianca
collection PubMed
description Serum paraoxonase-1 (PON1) is a member of the paraoxonases family (PON1, PON2, and PON3). PON1 is synthesized and secreted by the liver, and in circulation it is associated with HDL. PON1 has antioxidative properties, which are associated with the enzyme's capability to decrease oxidative stress in atherosclerotic lesions and to attenuate atherosclerosis development. Epidemiological evidence demonstrates that low PON1 activity is associated with increased risk of cardiovascular events and cardiovascular disease and is an independent risk factor for coronary artery disease. Therefore, pharmacological modulation of PON1 activity or PON1 gene expression could constitute a useful approach for preventing atherosclerosis. A primary determinant of serum PON1 levels is the availability of the enzyme for release by the liver, the principal site of PON1 production. Together with the enzyme secretion rate, enzymatic turnover, and protein stability, the level of PON1 gene expression is a major determinant of PON1 status. This paper summarizes recent progress in understanding the regulation of PON1 expression in hepatocytes.
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spelling pubmed-33241612012-04-30 Regulation of Hepatic Paraoxonase-1 Expression Fuhrman, Bianca J Lipids Review Article Serum paraoxonase-1 (PON1) is a member of the paraoxonases family (PON1, PON2, and PON3). PON1 is synthesized and secreted by the liver, and in circulation it is associated with HDL. PON1 has antioxidative properties, which are associated with the enzyme's capability to decrease oxidative stress in atherosclerotic lesions and to attenuate atherosclerosis development. Epidemiological evidence demonstrates that low PON1 activity is associated with increased risk of cardiovascular events and cardiovascular disease and is an independent risk factor for coronary artery disease. Therefore, pharmacological modulation of PON1 activity or PON1 gene expression could constitute a useful approach for preventing atherosclerosis. A primary determinant of serum PON1 levels is the availability of the enzyme for release by the liver, the principal site of PON1 production. Together with the enzyme secretion rate, enzymatic turnover, and protein stability, the level of PON1 gene expression is a major determinant of PON1 status. This paper summarizes recent progress in understanding the regulation of PON1 expression in hepatocytes. Hindawi Publishing Corporation 2012 2012-04-03 /pmc/articles/PMC3324161/ /pubmed/22548179 http://dx.doi.org/10.1155/2012/684010 Text en Copyright © 2012 Bianca Fuhrman. 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
Fuhrman, Bianca
Regulation of Hepatic Paraoxonase-1 Expression
title Regulation of Hepatic Paraoxonase-1 Expression
title_full Regulation of Hepatic Paraoxonase-1 Expression
title_fullStr Regulation of Hepatic Paraoxonase-1 Expression
title_full_unstemmed Regulation of Hepatic Paraoxonase-1 Expression
title_short Regulation of Hepatic Paraoxonase-1 Expression
title_sort regulation of hepatic paraoxonase-1 expression
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324161/
https://www.ncbi.nlm.nih.gov/pubmed/22548179
http://dx.doi.org/10.1155/2012/684010
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