Abstract

Pathological neovascularization in the eye is a leading cause of blindness in all age groups from retinopathy of prematurity (ROP) in children to age-related macular degeneration (AMD) in the elderly. Inhibiting neovascularization via antivascular endothelial growth factor (VEGF) drugs has been used for the effective treatment. However, anti-VEGF therapies may cause development of chorioretinal atrophy as they affect a physiological amount of VEGF essential for retinal homeostasis. Furthermore, anti-VEGF therapies are still ineffective in some cases, especially in patients with AMD. Hypoxia-inducible factor (HIF) is a strong regulator of VEGF induction under hypoxic and other stress conditions. Our previous reports have indicated that HIF is associated with pathological retinal neovascularization in murine models of ROP and AMD, and HIF inhibition suppresses neovascularization by reducing an abnormal increase in VEGF expression. Along with this, we attempted to find novel effective HIF inhibitors from natural foods of our daily lives. Food ingredients were screened for prospective HIF inhibitors in ocular cell lines of 661W and ARPE-19, and a murine AMD model was utilized for examining suppressive effects of the ingredients on retinal neovascularization. As a result, rice bran and its component, vitamin B6 showed inhibitory effects on HIF activation and suppressed VEGF mRNA induction under a CoCl2-induced pseudo-hypoxic condition. Dietary supplement of these significantly suppressed retinal neovascularization in the AMD model. These data suggest that rice bran could have promising therapeutic values in the management of pathological ocular neovascularization.

Highlights

  • Ocular pathological neovascularization is a leading cause of blindness worldwide [1,2]. It affects our lives in all age groups from children to elderly with various names of diseases such as retinopathy of prematurity (ROP), diabetic retinopathy (DR), retinal vein occlusion and age-related macular degeneration (AMD) [3]

  • Hypoxia-inducible factor (HIF) expression was observed in human choroidal neovascular membranes in patients with AMD [13,14], and retinal pigment epithelial (RPE) cells resided in those membranes were localized with the presence of HIF and vascular endothelial growth factor (VEGF) [14]

  • We found that only six samples consistently showed statistically significant inhibitory effects on HIF activation under a CoCl2-induced hypoxic condition (Table A2)

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Summary

Introduction

Ocular pathological neovascularization is a leading cause of blindness worldwide [1,2]. It affects our lives in all age groups from children to elderly with various names of diseases such as retinopathy of prematurity (ROP), diabetic retinopathy (DR), retinal vein occlusion and age-related macular degeneration (AMD) [3]. Hypoxia-inducible factor (HIF) plays a strong transcription regulator of VEGF induction under hypoxic and other stress conditions [8]. HIF expression was observed in human choroidal neovascular membranes in patients with AMD [13,14], and retinal pigment epithelial (RPE) cells resided in those membranes were localized with the presence of HIF and VEGF [14]

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