Resveratrol Inhibits Hypoxia-Induced Vascular Endothelial Growth Factor Expression and Pathological Neovascularization.
10.3349/ymj.2015.56.6.1678
- Author:
Christopher Seungkyu LEE
1
;
Eun Young CHOI
;
Sung Chul LEE
;
Hyoung Jun KOH
;
Joon Haeng LEE
;
Ji Hyung CHUNG
Author Information
1. The Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Severance Hospital, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Choroidal neovascularization;
hypoxia-inducible factor-1;
resveratrol;
retinal pigment epithelium;
vascular endothelial growth factor
- MeSH:
Adult;
Animals;
Anoxia/metabolism/physiopathology;
Cell Survival/drug effects;
Choroidal Neovascularization/*metabolism/pathology;
Humans;
Hypoxia-Inducible Factor 1, alpha Subunit/*drug effects/metabolism;
Mice;
Mice, Inbred C57BL;
Phosphatidylinositol 3-Kinases/antagonists & inhibitors/*physiology;
Proteasome Endopeptidase Complex;
Proto-Oncogene Proteins c-akt/antagonists & inhibitors/*physiology;
Retinal Pigment Epithelium/*drug effects/metabolism;
Signal Transduction;
Stilbenes/administration & dosage/*pharmacology;
TOR Serine-Threonine Kinases/antagonists & inhibitors/*physiology;
Ubiquitin;
Vascular Endothelial Growth Factor A/*drug effects/metabolism
- From:Yonsei Medical Journal
2015;56(6):1678-1685
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: To investigate the effects of resveratrol on the expression of hypoxia-inducible factor 1alpha (HIF-1alpha) and vascular endothelial growth factor (VEGF) in human adult retinal pigment epithelial (ARPE-19) cells, and on experimental choroidal neovascularization (CNV) in mice. MATERIALS AND METHODS: ARPE-19 cells were treated with different concentrations of resveratrol and then incubated under hypoxic conditions with subsequent evaluation of cell viability, expression of HIF-1alpha, and expression of VEGF. The effects of resveratrol on the synthesis and degradation of hypoxia-induced HIF-1alpha were evaluated using inhibitors of the PI3K/Akt/mTOR and the ubiquitin proteasome pathways. In animal studies, CNV lesions were induced in C57BL/6 mice by laser photocoagulation. After 7 days of oral administration of resveratrol or vehicle, which began one day after CNV induction, image analysis was used to measure CNV areas on choroidal flat mounts stained with isolectin IB4. RESULTS: In ARPE-19 cells, resveratrol significantly inhibited HIF-1alpha and VEGF in a dose-dependent manner, by blocking the PI3K/Akt/mTOR signaling pathway and by promoting proteasomal HIF-1alpha degradation. In mice experiments, orally administered resveratrol significantly inhibited CNV growth in a dose-dependent manner. CONCLUSION: Resveratrol may have therapeutic value in the management of diseases involving pathological neovascularization.
