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Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease

High-density lipoproteins (HDL) comprise a heterogeneous family of lipoprotein particles divided into subclasses that are determined by density, size and surface charge as well as protein composition. Epidemiological studies have suggested an inverse correlation between High-density lipoprotein-chol...

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Autores principales: Estrada-Luna, Diego, Ortiz-Rodriguez, María Araceli, Medina-Briseño, Lizett, Carreón-Torres, Elizabeth, Izquierdo-Vega, Jeannett Alejandra, Sharma, Ashutosh, Cancino-Díaz, Juan Carlos, Pérez-Méndez, Oscar, Belefant-Miller, Helen, Betanzos-Cabrera, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278283/
https://www.ncbi.nlm.nih.gov/pubmed/30360466
http://dx.doi.org/10.3390/molecules23112730
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author Estrada-Luna, Diego
Ortiz-Rodriguez, María Araceli
Medina-Briseño, Lizett
Carreón-Torres, Elizabeth
Izquierdo-Vega, Jeannett Alejandra
Sharma, Ashutosh
Cancino-Díaz, Juan Carlos
Pérez-Méndez, Oscar
Belefant-Miller, Helen
Betanzos-Cabrera, Gabriel
author_facet Estrada-Luna, Diego
Ortiz-Rodriguez, María Araceli
Medina-Briseño, Lizett
Carreón-Torres, Elizabeth
Izquierdo-Vega, Jeannett Alejandra
Sharma, Ashutosh
Cancino-Díaz, Juan Carlos
Pérez-Méndez, Oscar
Belefant-Miller, Helen
Betanzos-Cabrera, Gabriel
author_sort Estrada-Luna, Diego
collection PubMed
description High-density lipoproteins (HDL) comprise a heterogeneous family of lipoprotein particles divided into subclasses that are determined by density, size and surface charge as well as protein composition. Epidemiological studies have suggested an inverse correlation between High-density lipoprotein-cholesterol (HDL-C) levels and the risk of cardiovascular diseases and atherosclerosis. HDLs promote reverse cholesterol transport (RCT) and have several atheroprotective functions such as anti-inflammation, anti-thrombosis, and anti-oxidation. HDLs are considered to be atheroprotective because they are associated in serum with paraoxonases (PONs) which protect HDL from oxidation. Polyphenol consumption reduces the risk of chronic diseases in humans. Polyphenols increase the binding of HDL to PON1, increasing the catalytic activity of PON1. This review summarizes the evidence currently available regarding pharmacological and alternative treatments aimed at improving the functionality of HDL-C. Information on the effectiveness of the treatments has contributed to the understanding of the molecular mechanisms that regulate plasma levels of HDL-C, thereby promoting the development of more effective treatment of cardiovascular diseases. For that purpose, Scopus and Medline databases were searched to identify the publications investigating the impact of current therapies focused on high-density lipoproteins.
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spelling pubmed-62782832018-12-13 Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease Estrada-Luna, Diego Ortiz-Rodriguez, María Araceli Medina-Briseño, Lizett Carreón-Torres, Elizabeth Izquierdo-Vega, Jeannett Alejandra Sharma, Ashutosh Cancino-Díaz, Juan Carlos Pérez-Méndez, Oscar Belefant-Miller, Helen Betanzos-Cabrera, Gabriel Molecules Review High-density lipoproteins (HDL) comprise a heterogeneous family of lipoprotein particles divided into subclasses that are determined by density, size and surface charge as well as protein composition. Epidemiological studies have suggested an inverse correlation between High-density lipoprotein-cholesterol (HDL-C) levels and the risk of cardiovascular diseases and atherosclerosis. HDLs promote reverse cholesterol transport (RCT) and have several atheroprotective functions such as anti-inflammation, anti-thrombosis, and anti-oxidation. HDLs are considered to be atheroprotective because they are associated in serum with paraoxonases (PONs) which protect HDL from oxidation. Polyphenol consumption reduces the risk of chronic diseases in humans. Polyphenols increase the binding of HDL to PON1, increasing the catalytic activity of PON1. This review summarizes the evidence currently available regarding pharmacological and alternative treatments aimed at improving the functionality of HDL-C. Information on the effectiveness of the treatments has contributed to the understanding of the molecular mechanisms that regulate plasma levels of HDL-C, thereby promoting the development of more effective treatment of cardiovascular diseases. For that purpose, Scopus and Medline databases were searched to identify the publications investigating the impact of current therapies focused on high-density lipoproteins. MDPI 2018-10-23 /pmc/articles/PMC6278283/ /pubmed/30360466 http://dx.doi.org/10.3390/molecules23112730 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Estrada-Luna, Diego
Ortiz-Rodriguez, María Araceli
Medina-Briseño, Lizett
Carreón-Torres, Elizabeth
Izquierdo-Vega, Jeannett Alejandra
Sharma, Ashutosh
Cancino-Díaz, Juan Carlos
Pérez-Méndez, Oscar
Belefant-Miller, Helen
Betanzos-Cabrera, Gabriel
Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease
title Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease
title_full Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease
title_fullStr Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease
title_full_unstemmed Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease
title_short Current Therapies Focused on High-Density Lipoproteins Associated with Cardiovascular Disease
title_sort current therapies focused on high-density lipoproteins associated with cardiovascular disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278283/
https://www.ncbi.nlm.nih.gov/pubmed/30360466
http://dx.doi.org/10.3390/molecules23112730
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