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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Autores principales: Qiao YH, Zhu BL, Tian AJ, Li ZJ
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2017
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Acceso en línea:https://doaj.org/article/ffebd9edd7654815a5149bd3b3c94e28
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spelling oai:doaj.org-article:ffebd9edd7654815a5149bd3b3c94e282021-12-02T03:11:36ZPEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy1178-2013https://doaj.org/article/ffebd9edd7654815a5149bd3b3c94e282017-07-01T00:00:00Zhttps://www.dovepress.com/peg-coated-gold-nanoparticles-attenuate-beta-adrenergic-receptor-media-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Yuhui 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 pathwayQiao YHZhu BLTian AJLi ZJDove Medical PressarticleAuNPsCardiac hypertrophyβ-adrenergic receptorERK1/2 signalling pathwayMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 4709-4719 (2017)
institution DOAJ
collection DOAJ
language EN
topic AuNPs
Cardiac hypertrophy
β-adrenergic receptor
ERK1/2 signalling pathway
Medicine (General)
R5-920
spellingShingle AuNPs
Cardiac hypertrophy
β-adrenergic receptor
ERK1/2 signalling pathway
Medicine (General)
R5-920
Qiao YH
Zhu BL
Tian AJ
Li ZJ
PEG-coated gold nanoparticles attenuate β-adrenergic receptor-mediated cardiac hypertrophy
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
format article
author Qiao YH
Zhu BL
Tian AJ
Li ZJ
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
publishDate 2017
url https://doaj.org/article/ffebd9edd7654815a5149bd3b3c94e28
work_keys_str_mv AT qiaoyh pegcoatedgoldnanoparticlesattenuatebetaadrenergicreceptormediatedcardiachypertrophy
AT zhubl pegcoatedgoldnanoparticlesattenuatebetaadrenergicreceptormediatedcardiachypertrophy
AT tianaj pegcoatedgoldnanoparticlesattenuatebetaadrenergicreceptormediatedcardiachypertrophy
AT lizj pegcoatedgoldnanoparticlesattenuatebetaadrenergicreceptormediatedcardiachypertrophy
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