Abstract
Advanced glycation end products (AGEs) are involved in the development of diabetic complications such as diabetic retinopathy. 5′-methoxybiphenyl-3,4,3′-triol (referred to as K24) was isolated using bioactivity-guided fractionation of Osteomeles schwerinae C. K. Schneid. and identified as a potent AGE inhibitor. To identify the protective effect of K24 on disruption of the blood-retinal barrier, AGE-RSA was intravitreally injected into rat eyes. K24 had an inhibitory effect on AGE-RSA-induced retinal vascular leakage by suppressing the expression of vascular endothelial growth factor (VEGF) and decreasing the loss of occludin. In addition, we examined whether K24 has a preventive effect against retinal pathogenic angiogenesis in an oxygen-induced retinopathy (OIR) mouse model. K24 significantly reduced the retinal non-perfused area and neovascular tufts in the OIR mice. These data indicate that K24 could serve as an innovative pharmaceutical agent to prevent blood-retinal barrier breakage and retinal pathogenic angiogenesis through an anti-VEGF mechanism.
| Original language | English |
|---|---|
| Pages (from-to) | 172-178 |
| Number of pages | 7 |
| Journal | European Journal of Pharmacology |
| Volume | 760 |
| DOIs | |
| State | Published - 2015.08.5 |
Keywords
- 5′-Methoxybiphenyl-3,4,3′-triol
- Advanced glycation end products
- Blood-retinal barrier
- Oxygen-induced retinopathy
- Vascular endothelial growth factor
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