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Role of adiponectin in metabolic and cardiovascular disease

Under disease conditions including obesity (insulin resistance) and diabetes, dysregulation of adipokines such as tumor necrosis factor (TNF)-α, leptin, resistin, and adiponectin contribute to the development of metabolic and cardiovascular disease. Unlike other adipokines, adiponectin has been show...

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Autores principales: Lee, Sewon, Kwak, Hyo-Bum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Exercise Rehabilitation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4025550/
https://www.ncbi.nlm.nih.gov/pubmed/24877038
http://dx.doi.org/10.12965/jer.140100
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author Lee, Sewon
Kwak, Hyo-Bum
author_facet Lee, Sewon
Kwak, Hyo-Bum
author_sort Lee, Sewon
collection PubMed
description Under disease conditions including obesity (insulin resistance) and diabetes, dysregulation of adipokines such as tumor necrosis factor (TNF)-α, leptin, resistin, and adiponectin contribute to the development of metabolic and cardiovascular disease. Unlike other adipokines, adiponectin has been shown to be a therapeutic target for metabolic syndrome and cardiovascular disease. Circulating levels of adiponectin are markedly reduced in obese, diabetic, hypertensive, and coronary artery disease patients as well as experimental animal models of insulin resistance and diabetes. Recently, the small molecule adiponectin receptors (AdipoRs) agonist was discovered and suggested that the agonist is a novel therapeutic target for the treatment of type 2 diabetes linked to obesity in an experimental mouse model. This review will focus on signaling pathways involved in adiponectin and its receptors and the role of adiponectin in metabolic and cardiovascular disease including insulin resistance, cardiomyopathy, and cardiovascular dysfunction.
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spelling pubmed-40255502014-05-29 Role of adiponectin in metabolic and cardiovascular disease Lee, Sewon Kwak, Hyo-Bum J Exerc Rehabil Review Article Under disease conditions including obesity (insulin resistance) and diabetes, dysregulation of adipokines such as tumor necrosis factor (TNF)-α, leptin, resistin, and adiponectin contribute to the development of metabolic and cardiovascular disease. Unlike other adipokines, adiponectin has been shown to be a therapeutic target for metabolic syndrome and cardiovascular disease. Circulating levels of adiponectin are markedly reduced in obese, diabetic, hypertensive, and coronary artery disease patients as well as experimental animal models of insulin resistance and diabetes. Recently, the small molecule adiponectin receptors (AdipoRs) agonist was discovered and suggested that the agonist is a novel therapeutic target for the treatment of type 2 diabetes linked to obesity in an experimental mouse model. This review will focus on signaling pathways involved in adiponectin and its receptors and the role of adiponectin in metabolic and cardiovascular disease including insulin resistance, cardiomyopathy, and cardiovascular dysfunction. Korean Society of Exercise Rehabilitation 2014-04-30 /pmc/articles/PMC4025550/ /pubmed/24877038 http://dx.doi.org/10.12965/jer.140100 Text en Copyright © 2014 Korean Society of Exercise Rehabilitation This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Lee, Sewon
Kwak, Hyo-Bum
Role of adiponectin in metabolic and cardiovascular disease
title Role of adiponectin in metabolic and cardiovascular disease
title_full Role of adiponectin in metabolic and cardiovascular disease
title_fullStr Role of adiponectin in metabolic and cardiovascular disease
title_full_unstemmed Role of adiponectin in metabolic and cardiovascular disease
title_short Role of adiponectin in metabolic and cardiovascular disease
title_sort role of adiponectin in metabolic and cardiovascular disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4025550/
https://www.ncbi.nlm.nih.gov/pubmed/24877038
http://dx.doi.org/10.12965/jer.140100
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