Role of quercetin in modulating rat cardiomyocyte gene expression profile

被引:40
作者
Angeloni, C. [1 ]
Leoncini, E. [1 ]
Malaguti, M. [1 ]
Angelini, S. [2 ]
Hrelia, P. [2 ]
Hrelia, S. [1 ]
机构
[1] Univ Bologna, Dipartimento Biochim G Moruzzi, Alma Mater Studiorum, I-40126 Bologna, Italy
[2] Univ Bologna, Dept Pharmacol, I-40126 Bologna, Italy
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2008年 / 294卷 / 03期
关键词
flavonoids; phase; 2; enzymes; oxidative stress;
D O I
10.1152/ajpheart.01091.2007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite extensive studies, the fundamental mechanisms responsible for the development and progression of cardiovascular diseases have not yet been fully elucidated. Recent experimental and clinical studies have suggested that reactive oxygen species play a major pathological role. Oxidative stress reduction induced by flavonoids has been regarded by many as the most likely mechanism in the protective effects of these compounds; however, there is an emerging view that flavonoids may also exert modulatory actions on protein kinase and lipid kinase signaling pathways. Quercetin, a major flavonoid present in the human diet, has been widely studied, and its biological properties are consistent with its protective role in the cardiovascular system. However, it remains unknown whether the cardioprotective effects of quercetin may also occur through the modulation of genes involved in cell survival. The main goal of this study was to examine the gene expression profiling of cultured rat primary cardiomyocytes treated with quercetin using DNA microarrays and to relate these data to functional effects. Results showed distinct temporal changes in gene expression induced by quercetin and a strong upregulation of phase 2 enzymes, highlighting quercetin ability to act also with an indirect antioxidant mechanism.
引用
收藏
页码:H1233 / H1243
页数:11
相关论文
共 66 条
[61]   Expression of glutathione-S-transferase isozyme in the SY5Y neuroblastoma cell, line increases resistance to oxidative stress [J].
Xie, CS ;
Lovell, MA ;
Xiong, SL ;
Kindy, MS ;
Guo, JT ;
Xie, J ;
Amaranth, V ;
Montine, TJ ;
Markesbery, WR .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (01) :73-81
[62]   Thioredoxin - A key regulator of cardiovascular homeostasis [J].
Yamawaki, H ;
Haendeler, J ;
Berk, BC .
CIRCULATION RESEARCH, 2003, 93 (11) :1029-1033
[63]   Role of glutathione S-transferases in protection against lipid peroxidation -: Overexpression of hgsta2-2 in k562 cells protects against hydrogen peroxide-induced apoptosis and inhibits JNK and caspase 3 activation [J].
Yang, Y ;
Cheng, JZ ;
Singhal, SS ;
Saini, M ;
Pandya, U ;
Awasthi, S ;
Awasthi, YC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) :19220-19230
[64]   Hypoxia induces severe right ventricular dilatation and infarction in heme oxygenase-1 null mice [J].
Yet, SF ;
Perrella, MA ;
Layne, MD ;
Hsieh, CM ;
Maemura, K ;
Kobzik, L ;
Wiesel, P ;
Christou, H ;
Kourembanas, S ;
Lee, ME .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (08) :R23-R29
[65]   Cardiac-specific expression of heme oxygenase-1 protects against ischemia and reperfusion injury in transgenic mice [J].
Yet, SF ;
Tian, R ;
Layne, MD ;
Wang, ZY ;
Maemura, K ;
Solovyeva, M ;
Ith, B ;
Melo, LG ;
Zhang, LN ;
Ingwall, JS ;
Dzau, VJ ;
Lee, ME ;
Perrella, MA .
CIRCULATION RESEARCH, 2001, 89 (02) :168-173
[66]   KINETIC-ANALYSIS OF THE INTRACELLULAR CONJUGATION OF MONOCHLOROBIMANE BY IC-21 MURINE MACROPHAGE GLUTATHIONE-S-TRANSFERASE [J].
YOUNG, PR ;
WHITE, ALC ;
DZIDO, GA .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1994, 1201 (03) :461-465