3,4-Dihydroxybenzaldehyde purified from the barley seeds (Hordeum vulgare) inhibits oxidative DNA damage and apoptosis via its antioxidant activity

被引:52
|
作者
Jeong, Jin Boo [1 ]
Hong, Se Chul [1 ]
Jeong, Hyung Jin [1 ]
机构
[1] Andong Natl Univ, Coll Nat Sci, Andong, South Korea
基金
新加坡国家研究基金会;
关键词
3; 4-Dihydroxybenzaldehyde; Barley seeds (Hordeum vulgare) Antioxidants; Cancer chemoprevention; Oxidative DNA damage; Apoptosis; Reactive oxygen species (ROS); HYDROGEN-PEROXIDE; ASCORBIC-ACID; FLAVONOIDS; H2AX;
D O I
10.1016/j.phymed.2008.09.013
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Barley is a major crop worldwide. It has been reported that barley seeds have an effect on scavenging ROS. However, little has been known about the functional role of the barley on the inhibition of DNA damage and apoptosis by ROS. In this study, we purified 3,4-dihydroxybenzaldehyde from the barley with silica get column chromatography and HPLC and then identified it by GC/MS. And we firstly investigated the inhibitory effects of 3,4-dihydroxybenzaldehyde purified from the barley on oxidative DNA damage and apoptosis induced by H2O2, the major mediator of oxidative stress and a potent mutagen. In antioxidant activity assay such as DPPH radical and hydroxyl radical scavenging assay, Fe2+ chelating assay, and intracellular ROS scavenging assay by DCF-DA, 3,4-dihydroxybenzaldehyde was found to scavenge DPPH radical, hydroxyl radical and intracellular ROS. Also it chelated Fe2+. In in vitro oxidative DNA damage assay and the expression level of phospho-H2A.X, it inhibited oxidative DNA damage and its treatment decreased the expression level of phospho-H2A.X. And in oxidative cell death and apoptosis assay via MTT assay and Hoechst 33342 staining, respectively, the treatment of 3,4-dihydroxybenzaldehyde attenuated H2O2-induced cell death and apoptosis. These results suggest that the barley may exert the inhibitory effect on H2O2-induced tumor development by blocking H2O2-induced oxidative DNA damage, cell death and apoptosis. Crown Copyright (C) 2008 Published by Elsevier GmbH. All rights reserved.
引用
收藏
页码:85 / 94
页数:10
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