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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on October 29, 2007; DOI: 10.1124/jpet.107.132720


0022-3565/08/3242-643-647$20.00
JPET 324:643-647, 2008
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CARDIOVASCULAR

Antiangiogenic Effect of Deguelin on Choroidal Neovascularization

Jeong Hun Kim, Jin Hyoung Kim, Young Suk Yu, Kyu Hyung Park, Hye Jin Kang, Ho-Young Lee, and Kyu-Won Kim

Department of Ophthalmology, College of Medicine, Seoul National University and Seoul Artificial Eye Center Clinical Research Institute, Seoul National University Hospital, Seoul, Korea (J.Hu.K., J.Hy.K., Y.S.Y.); Department of Ophthalmology, College of Medicine, Seoul National University and Bundang Seoul National University Hospital, Seong-nam, Korea (K.H.P.); NeuroVascular Coordination Research Center, College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea (H.J.K., K.-W.K.); and Department of Thoracic/Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas (H.-Y.L.)

Age-related macular degeneration is the leading cause of blindness in the elderly. Choroidal neovascularization (CNV) leads to severe vision loss in patients of age-related macular degeneration. Previously, we have demonstrated that deguelin, isolated from plants in the Mundulea sericea family, is a chemopreventive agent. This study evaluates the antiangiogenic effect of deguelin on CNV. The toxicity of deguelin was evaluated through 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay in human umbilical vein endothelial cells (HUVECs) as well as histological examination and terminal deoxynucleotidyl transferase dUTP nick-end labeling staining in the deguelin-injected retina. Antiangiogenic activity of deguelin was evaluated by in vitro tube formation assay of HUVECs and in vivo angiogenesis of chick chorioallantoic membrane (CAM). In C57BL/6 mice with laser-induced CNV, deguelin or phosphate-buffered saline was injected intravitreously. CNV lesions were examined by fluorescence angiography and vessel counting in cross-sections. Deguelin showed no effect on cell viability of HUVECs and no retinal toxicity in a concentration range of 0.01 to 1 µM. Deguelin effectively inhibited in vitro tube formation of HUVECs and in vivo angiogenesis of CAM. Interestingly, deguelin significantly reduced CNV and its leakage in mouse model of laser photocoagulation-induced CNV. Our data suggests that deguelin is a potent inhibitor of CNV and may be applied in the treatment of other vasoproliferative retinopathies such as retinopathy of prematurity and diabetic retinopathy.


Received October 7, 2007; accepted October 26, 2007.

Address correspondence to: Dr. Young Suk Yu, Department of Ophthalmology, College of Medicine, Seoul National University and Seoul Artificial Eye Center Clinical Research Institute, Seoul National University Hospital, Seoul 151-744, Republic of Korea. E-mail: ysyu{at}snu.ac.kr







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