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Effect of guibi-tang, a traditional herbal formula, on retinal neovascularization in a mouse model of proliferative retinopathy

  • Yun Mi Lee
  • , Yu Ri Lee
  • , Chan Sik Kim
  • , Kyuhyung Jo
  • , Eunjin Sohn
  • , Jin Kim
  • , Junghyun Kim*
  • *Corresponding author for this work
  • Korea Institute of Oriental Medicine

Research output: Contribution to journalJournal articlepeer-review

Abstract

Ocular pathologic angiogenesis is an important causative risk factor of blindness in retinopathy of prematurity, proliferative diabetic retinopathy, and neovascular macular degeneration. Guibi-tang (GBT) is a frequently used oriental herbal formula in East Asian countries, and is also called Qui-pi-tang in Chinese and Kihi-To in Japanese. In the present study, we investigated the preventive effect of GBT on retinal pathogenic neovascularization in a mouse model of oxygen-induced retinopathy (OIR). C57BL/6 mice were exposed to 75% hyperoxia for five days on postnatal day 7 (P7). The mice were then exposed to room air from P12 to P17 to induce ischemic proliferative retinopathy. GBT (50 or 100 mg/kg/day) was intraperitoneally administered daily for five days (from P12 to P16). On P17, Retinal neovascularization was measured on P17, and the expression levels of 55 angiogenesis-related factors were analyzed using protein arrays. GBT significantly decreased retinal pathogenic angiogenesis in OIR mice, and protein arrays revealed that GBT decreased PAI-1 protein expression levels. Quantitative real-time PCR revealed that GBT reduced vascular endothelial growth factor (VEGF), fibroblast growth factor 2 (FGF2), and plasminogen activator inhibitor 1 (PAI-1) mRNA levels in OIR mice. GBT promotes potent inhibitory activity for retinal neovascularization by decreasing VEGF, FGF2, and PAI-1 levels.

Original languageEnglish
Pages (from-to)29900-29910
Number of pages11
JournalInternational Journal of Molecular Sciences
Volume16
Issue number12
DOIs
StatePublished - 2015.12.16

Keywords

  • Fibroblast growth factor 2
  • Oxygen-induced retinopathy
  • Plasminogen activator inhibitor 1
  • Retinal neovascularization
  • Vascular endothelial growth factor

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