Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis

Hydroxyoctadecadienoic acids (HODEs) are stable oxidation products of linoleic acid, the generation of which is increased where oxidative stress is increased, such as in diabetes. In early atherosclerosis, 13-HODE is generated in macrophages by 15-lipoxygenase-1. This enhances protective mechanisms...

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Main Authors: Venkat Vangaveti, Bernhard T. Baune, R. Lee Kennedy
Format: Article
Language:English
Published: SAGE Publishing 2010-06-01
Series:Therapeutic Advances in Endocrinology and Metabolism
Online Access:https://doi.org/10.1177/2042018810375656
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spelling doaj-592dc33e8f6e478b97b5de9e02bd28232020-11-25T03:15:28ZengSAGE PublishingTherapeutic Advances in Endocrinology and Metabolism2042-01882010-06-01110.1177/2042018810375656Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesisVenkat VangavetiBernhard T. BauneR. Lee KennedyHydroxyoctadecadienoic acids (HODEs) are stable oxidation products of linoleic acid, the generation of which is increased where oxidative stress is increased, such as in diabetes. In early atherosclerosis, 13-HODE is generated in macrophages by 15-lipoxygenase-1. This enhances protective mechanisms through peroxisome proliferator-activated receptor (PPAR)-γ activation leading to increased clearance of lipid and lipid-laden cells from the arterial wall. In later atherosclerosis, both 9-HODE and 13-HODE are generated nonenzymatically. At this stage, early protective mechanisms are overwhelmed and pro-inflammatory effects of 9-HODE, acting through the receptor GPR132, and increased apoptosis predominate leading to a fragile, acellular plaque. Increased HODE levels thus contribute to atherosclerosis progression and the risk of clinical events such as myocardial infarction or stroke. Better understanding of the role of HODEs may lead to new pharmacologic approaches to modulate their production or action, and therefore lessen the burden of atherosclerotic disease in high-risk patients.https://doi.org/10.1177/2042018810375656
collection DOAJ
language English
format Article
sources DOAJ
author Venkat Vangaveti
Bernhard T. Baune
R. Lee Kennedy
spellingShingle Venkat Vangaveti
Bernhard T. Baune
R. Lee Kennedy
Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis
Therapeutic Advances in Endocrinology and Metabolism
author_facet Venkat Vangaveti
Bernhard T. Baune
R. Lee Kennedy
author_sort Venkat Vangaveti
title Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis
title_short Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis
title_full Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis
title_fullStr Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis
title_full_unstemmed Review: Hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis
title_sort review: hydroxyoctadecadienoic acids: novel regulators of macrophage differentiation and atherogenesis
publisher SAGE Publishing
series Therapeutic Advances in Endocrinology and Metabolism
issn 2042-0188
publishDate 2010-06-01
description Hydroxyoctadecadienoic acids (HODEs) are stable oxidation products of linoleic acid, the generation of which is increased where oxidative stress is increased, such as in diabetes. In early atherosclerosis, 13-HODE is generated in macrophages by 15-lipoxygenase-1. This enhances protective mechanisms through peroxisome proliferator-activated receptor (PPAR)-γ activation leading to increased clearance of lipid and lipid-laden cells from the arterial wall. In later atherosclerosis, both 9-HODE and 13-HODE are generated nonenzymatically. At this stage, early protective mechanisms are overwhelmed and pro-inflammatory effects of 9-HODE, acting through the receptor GPR132, and increased apoptosis predominate leading to a fragile, acellular plaque. Increased HODE levels thus contribute to atherosclerosis progression and the risk of clinical events such as myocardial infarction or stroke. Better understanding of the role of HODEs may lead to new pharmacologic approaches to modulate their production or action, and therefore lessen the burden of atherosclerotic disease in high-risk patients.
url https://doi.org/10.1177/2042018810375656
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