Abstract |
The antioxidant activity of genistein is associated with preventing atherosclerosis; however, the underlying mechanisms are not fully understood. In this study, human umbilical vein endothelial cells (HUVECs) were pretreated with genistein at different concentrations (10nM, 100nM and 1000nM) for 6h and then exposed to ox-LDL (50mg/L) for another 24h. Results showed that genistein restrained reactive oxygen species (ROS) and malondialdehyde (MDA) production, and ameliorated the inhibitory effect on superoxide dismutase (SOD), catalase (CAT), glutathione (GSH) and glutathione peroxidase (GPx) activity elicited by ox-LDL stimulation. The effects of genistein were correlated with the upregulation of sirtuin-1 via inhibiting miR-34a, and were abolished by sirtuin-1 siRNA or miR-34a mimic. Moreover, the antioxidation of genistein was associated with miR-34a/ sirtuin-1-mediated nuclear translocation and deacetylation of foxo3a, accompanying with the enhanced expressions of MnSOD and CAT. The present study suggests that miR-34a/ sirtuin-1/foxo3a might play an important role in genistein reversing ox-LDL-induced oxidative damage in HUVECs.
|
Authors | Huaping Zhang, Zhenxiang Zhao, Xuefen Pang, Jian Yang, Haixia Yu, Yinhong Zhang, Hui Zhou, Jiahui Zhao |
Journal | Toxicology letters
(Toxicol Lett)
Vol. 277
Pg. 115-122
(Aug 05 2017)
ISSN: 1879-3169 [Electronic] Netherlands |
PMID | 28688900
(Publication Type: Journal Article)
|
Copyright | Copyright © 2017 Elsevier B.V. All rights reserved. |
Chemical References |
- Antioxidants
- FOXO3 protein, human
- Forkhead Box Protein O3
- Lipoproteins, LDL
- MIRN34 microRNA, human
- MicroRNAs
- oxidized low density lipoprotein
- Genistein
- Catalase
- Glutathione Peroxidase
- Superoxide Dismutase
- SIRT1 protein, human
- Sirtuin 1
- Glutathione
|
Topics |
- Acetylation
- Active Transport, Cell Nucleus
- Antioxidants
(pharmacology)
- Catalase
(metabolism)
- Cells, Cultured
- Cytoprotection
- Dose-Response Relationship, Drug
- Forkhead Box Protein O3
(genetics, metabolism)
- Genistein
(pharmacology)
- Glutathione
(metabolism)
- Glutathione Peroxidase
(metabolism)
- Human Umbilical Vein Endothelial Cells
(drug effects, enzymology, pathology)
- Humans
- Lipoproteins, LDL
(toxicity)
- MicroRNAs
(genetics, metabolism)
- Oxidative Stress
(drug effects)
- RNA Interference
- Signal Transduction
(drug effects)
- Sirtuin 1
(genetics, metabolism)
- Superoxide Dismutase
(metabolism)
- Transfection
|