RETRACTED: Phytoestrogen α-zearalanol inhibits homocysteine-induced endothelin-1 expression and oxidative stress in human umbilical vein endothelial cells (Retracted Article)

被引:21
|
作者
Duan, Jinhong [1 ]
Xu, Haishan [1 ]
Dai, Shunling [1 ]
Wang, Xiaoming [1 ]
Wu, Yunqing [1 ]
Zhang, Yandong [1 ]
Sun, Renyu [1 ]
Ren, Jun [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Peking Union Med Coll, Fac Basic Med, Beijing 100005, Peoples R China
[2] Univ Wyoming, Sch Pharm, Laramie, WY 82071 USA
基金
中国国家自然科学基金;
关键词
phytoestrogen; alpha-ZAL; homocysteine; endothelin-1; oxidative stress; AP-1;
D O I
10.1016/j.atherosclerosis.2007.08.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although estrogen replacement therapy may improve dampened endothelial function in postmenopausal women, the associated risk of breast and ovarian cancer has limited its long-term use. Identifying effective alternative remedy with less carcinogenicity is in serious demand. This study was designed to examine the effect of the phytoestrogen alpha-zearalanol (alpha-ZAL) on homocysteine-induced endothelin-1 (ETL-1) induction, reactive oxygen species (ROS) production and transcription pathways in human umbilical vein endothelial cells (HUVECs). ROS was measured by DCF fluorescent microscopy. Homocysteine-induced expression of ET-1 mRNA, ERK, pERK and c-jun/AP-1 protein was measured using RT-PCR and Western blot analysis, respectively. ET-1 secretion was determined by the enzymatic immunoassay. Transcriptional factor AP-1 expression in response to alpha-ZAL, homocysteine or both was evaluated by transient transfection assay. Our data revealed that alpha-ZAL ablated homocysteine-elicited ET-1 secretion, upregulated ET-1 mRNA and homocysteine-induced ROS accumulation without any effects by itself. alpha-ZAL also nullified homocysteine-induced increase in c-Jun/AP-1 expression/activity without eliciting any effect by itself. Collectively, our data indicated that alpha-ZAL may antagonize homocysteine-induced ET-1 gene induction, ROS accumulation, activation of ERK signaling pathway and AP-1 transcriptional factor, all of which may contribute to alpha-ZAL-induced beneficial effect on endothelial function. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:549 / 555
页数:7
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