Chlorogenic acid improves ex vivo vessel function and protects endothelial cells against HOCl-induced oxidative damage, via increased production of nitric oxide and induction of Hmox-1

被引:75
作者
Jiang, Rujia [1 ]
Hodgson, Jonathan M. [1 ]
Mas, Emilie [1 ]
Croft, Kevin D. [1 ]
Ward, Natalie C. [1 ,2 ,3 ]
机构
[1] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6000, Australia
[2] Curtin Univ, Sch Biomed Sci, Perth, WA 6845, Australia
[3] Curtin Univ, Curtin Hlth Innovat Res Inst, Perth, WA 6845, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Polyphenols; Chlorogenic acid; Endothelial function; Nitric oxide; Oxidative stress; Heme oxygenase-1; HIGH-FAT DIET; E-KNOCKOUT MICE; HEME OXYGENASE-1; VASCULAR-DISEASES; CARBON-MONOXIDE; IN-VIVO; DYSFUNCTION; COFFEE; POLYPHENOLS; SYNTHASE;
D O I
10.1016/j.jnutbio.2015.08.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Dietary polyphenols are potential contributors toward improved cardiovascular health. Coffee is one of the richest sources of dietary polyphenols in a coffee-drinking population, the most abundant form being chlorogenic acid (CGA). Endothelial dysfunction is an early and major risk factor for cardiovascular disease. Nitric oxide (NO) is a key factor in regulation of endothelial function. Heme oxygenase-1 (Hmox-1), an inducible isoform of heme oxygenase that is produced in response to stressors such as oxidative stress, may also play a role in vascular protection. The aim of this study was to investigate the effect of CGA on endothelial function with oxidant-induced damage in isolated aortic rings from C57BL mice. We further examine the mechanism by investigating cell viability, activation of eNOS and induction of Hmox-1 in human aortic endothelial cells (HAECs). We found that pretreatment of isolated aortic rings with 10-mu M CGA-protected vessels against HOCl-induced endothelial dysfunction (P<0.05). Pretreatment of cultured HAECs with 10-mu M CGA increased endothelial cell viability following exposure to HOCl (P<0.05). Moreover, CGA increased NO production in HAECs in a dose-dependent manner, peaking at 6 h (P<0.05). CGA at 5 mu M and 10 mu M increased eNOS dimerization at 6 h and induced Hmox-1 protein expression at 6 h and 24 h in HAECs. These results are consistent with the cardiovascular protective effects of coffee polyphenols and demonstrate that CGA can protect vessels and cultured endothelial cells against oxidant-induced damage. The mechanism behind the beneficial effect of CGA appears to be in part via increased production of NO and induction of Hmox-1. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:53 / 60
页数:8
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