PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy

Yuhui Qiao, Baoling Zhu, Aiju Tian, Zijian Li Department of Cardiology, Institute of Vascular Medicine, Peking University Third Hospital, Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Ministry of Health, Key Laboratory of Molecular Cardiovascular Sciences, Ministry of...

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Main Authors: Qiao YH, Zhu BL, Tian AJ, Li ZJ
Format: Article
Language:English
Published: Dove Medical Press 2017-07-01
Series:International Journal of Nanomedicine
Subjects:
Online Access:https://www.dovepress.com/peg-coated-gold-nanoparticles-attenuate-beta-adrenergic-receptor-media-peer-reviewed-article-IJN
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spelling doaj-ffebd9edd7654815a5149bd3b3c94e282020-11-25T00:37:18ZengDove Medical PressInternational Journal of Nanomedicine1178-20132017-07-01Volume 124709471933557PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophyQiao YHZhu BLTian AJLi ZJYuhui Qiao, Baoling Zhu, Aiju Tian, Zijian Li Department of Cardiology, Institute of Vascular Medicine, Peking University Third Hospital, Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Ministry of Health, Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education and Beijing Key Laboratory of Cardiovascular Receptors Research, Beijing, People’s Republic of China Abstract: Gold nanoparticles (AuNPs) are widely used as a drug delivery vehicle, which can accumulate in the heart through blood circulation. Therefore, it is very important to understand the effect of AuNPs on the heart, especially under pathological conditions. In this study, we found that PEG-coated AuNPs attenuate β-adrenergic receptor (β-AR)-mediated acute cardiac hypertrophy and inflammation. However, both isoproterenol, a non-selective β-AR agonist, and AuNPs did not induce cardiac function change or cardiac fibrosis. AuNPs exerted an anti-cardiac hypertrophy effect by decreasing β1-AR expression and its downstream ERK1/2 hypertrophic pathway. Our results indicated that AuNPs might be safe and have the potential to be used as multi-functional materials (drug carrier systems and anti-cardiac hypertrophy agents). Keywords: AuNPs, cardiac hypertrophy, β-adrenergic receptor, ERK1/2 signaling pathwayhttps://www.dovepress.com/peg-coated-gold-nanoparticles-attenuate-beta-adrenergic-receptor-media-peer-reviewed-article-IJNAuNPsCardiac hypertrophyβ-adrenergic receptorERK1/2 signalling pathway
collection DOAJ
language English
format Article
sources DOAJ
author Qiao YH
Zhu BL
Tian AJ
Li ZJ
spellingShingle Qiao YH
Zhu BL
Tian AJ
Li ZJ
PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
International Journal of Nanomedicine
AuNPs
Cardiac hypertrophy
β-adrenergic receptor
ERK1/2 signalling pathway
author_facet Qiao YH
Zhu BL
Tian AJ
Li ZJ
author_sort Qiao YH
title PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
title_short PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
title_full PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
title_fullStr PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
title_full_unstemmed PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
title_sort peg-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
publisher Dove Medical Press
series International Journal of Nanomedicine
issn 1178-2013
publishDate 2017-07-01
description Yuhui Qiao, Baoling Zhu, Aiju Tian, Zijian Li Department of Cardiology, Institute of Vascular Medicine, Peking University Third Hospital, Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Ministry of Health, Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education and Beijing Key Laboratory of Cardiovascular Receptors Research, Beijing, People’s Republic of China Abstract: Gold nanoparticles (AuNPs) are widely used as a drug delivery vehicle, which can accumulate in the heart through blood circulation. Therefore, it is very important to understand the effect of AuNPs on the heart, especially under pathological conditions. In this study, we found that PEG-coated AuNPs attenuate β-adrenergic receptor (β-AR)-mediated acute cardiac hypertrophy and inflammation. However, both isoproterenol, a non-selective β-AR agonist, and AuNPs did not induce cardiac function change or cardiac fibrosis. AuNPs exerted an anti-cardiac hypertrophy effect by decreasing β1-AR expression and its downstream ERK1/2 hypertrophic pathway. Our results indicated that AuNPs might be safe and have the potential to be used as multi-functional materials (drug carrier systems and anti-cardiac hypertrophy agents). Keywords: AuNPs, cardiac hypertrophy, β-adrenergic receptor, ERK1/2 signaling pathway
topic AuNPs
Cardiac hypertrophy
β-adrenergic receptor
ERK1/2 signalling pathway
url https://www.dovepress.com/peg-coated-gold-nanoparticles-attenuate-beta-adrenergic-receptor-media-peer-reviewed-article-IJN
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