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Human paraoxonase 2

Human paraoxonase 2 (PON2), which is a member of the paraoxonase family, possesses unique properties that distinguish it from PON1 and PON3. PON2 is ubiquitously expressed in many different tissue types and is highly expressed in the vital organs, such as the heart and lungs. Early research revealed...

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Autores principales: Porntadavity, Sureerut, Permpongpaiboon, Thinnakorn, Sukketsiri, Wanida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698900/
https://www.ncbi.nlm.nih.gov/pubmed/29255397
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author Porntadavity, Sureerut
Permpongpaiboon, Thinnakorn
Sukketsiri, Wanida
author_facet Porntadavity, Sureerut
Permpongpaiboon, Thinnakorn
Sukketsiri, Wanida
author_sort Porntadavity, Sureerut
collection PubMed
description Human paraoxonase 2 (PON2), which is a member of the paraoxonase family, possesses unique properties that distinguish it from PON1 and PON3. PON2 is ubiquitously expressed in many different tissue types and is highly expressed in the vital organs, such as the heart and lungs. Early research revealed that PON2 is exclusively intracellularly found, wherein it functions as an anti-oxidative protein by reducing intracellular and local oxidative stress. Studies in the last five years have demonstrated that PON2 protects against atherosclerosis by preventing low-density lipoprotein (LDL) oxidation, reversing the oxidation of mildly oxidised LDL, inhibiting monocyte chemotaxis, and increasing cholesterol efflux. Recently, emerging evidence has proposed that PON2 is an anti-atherosclerotic and may be associated with cardiovascular disease (CVD). The number of investigations concerning the relationship between two common PON2 polymorphisms and CVD among different ethnic groups and regions is rapidly growing. Here, we briefly review the developments in PON2 research by focusing on past and recent findings.
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spelling pubmed-56989002017-12-18 Human paraoxonase 2 Porntadavity, Sureerut Permpongpaiboon, Thinnakorn Sukketsiri, Wanida EXCLI J Review Article Human paraoxonase 2 (PON2), which is a member of the paraoxonase family, possesses unique properties that distinguish it from PON1 and PON3. PON2 is ubiquitously expressed in many different tissue types and is highly expressed in the vital organs, such as the heart and lungs. Early research revealed that PON2 is exclusively intracellularly found, wherein it functions as an anti-oxidative protein by reducing intracellular and local oxidative stress. Studies in the last five years have demonstrated that PON2 protects against atherosclerosis by preventing low-density lipoprotein (LDL) oxidation, reversing the oxidation of mildly oxidised LDL, inhibiting monocyte chemotaxis, and increasing cholesterol efflux. Recently, emerging evidence has proposed that PON2 is an anti-atherosclerotic and may be associated with cardiovascular disease (CVD). The number of investigations concerning the relationship between two common PON2 polymorphisms and CVD among different ethnic groups and regions is rapidly growing. Here, we briefly review the developments in PON2 research by focusing on past and recent findings. Leibniz Research Centre for Working Environment and Human Factors 2010-11-26 /pmc/articles/PMC5698900/ /pubmed/29255397 Text en Copyright © 2010 Porntadavity et al. http://www.excli.de/documents/assignment_of_rights.pdf This is an Open Access article distributed under the following Assignment of Rights http://www.excli.de/documents/assignment_of_rights.pdf. You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Review Article
Porntadavity, Sureerut
Permpongpaiboon, Thinnakorn
Sukketsiri, Wanida
Human paraoxonase 2
title Human paraoxonase 2
title_full Human paraoxonase 2
title_fullStr Human paraoxonase 2
title_full_unstemmed Human paraoxonase 2
title_short Human paraoxonase 2
title_sort human paraoxonase 2
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698900/
https://www.ncbi.nlm.nih.gov/pubmed/29255397
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