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Cited 88 time in webofscience Cited 95 time in scopus
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Resveratrol blocks diabetes-induced early vascular lesions and vascular endothelial growth factor induction in mouse retinas

Authors
Kim, Young HeeKim, Yoon SookRoh, Gu SeobChoi, Wan SungCho, Gyeong Jae
Issue Date
Feb-2012
Publisher
Wiley-Blackwell
Keywords
diabetic retinopathy; early diabetes; pericyte loss; resveratrol; retina; vascular endothelial growth factor; vascular lesions; vessel leakage
Citation
Acta Ophthalmologica, v.90, no.1, pp E31 - E37
Indexed
SCI
SCIE
SCOPUS
Journal Title
Acta Ophthalmologica
Volume
90
Number
1
Start Page
E31
End Page
E37
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/22375
DOI
10.1111/j.1755-3768.2011.02243.x
ISSN
1755-375X
1755-3768
Abstract
Purpose: Vessel leakage and loss of pericytes are early signs of diabetic retinopathy (DR), which leads to vision loss. Upregulation of the vascular endothelial growth factor (VEGF) during diabetes plays a key role in mediating these vascular lesions. The aim of this study is to investigate the effects of resveratrol, a natural plant-derived phytoalexin, on vascular damage and VEGF induction in mouse retinas of early diabetes. Methods: Diabetes was induced in C57BL/6 mice by five consecutive-intraperitoneal injections of 55 mg/kg of streptozotocin (STZ). Animals injected with buffer only were used as controls. Beginning 1 month after the fifth injection of STZ or buffer, 20 mg/kg of resveratrol was administered by oral gavage daily for 4 weeks to diabetic and control mice, and all mice were killed 2 months after the injections. We assessed vessel leakage, pericyte loss and VEGF protein expression in mouse retinas of 2-month diabetes compared with controls with or without resveratrol treatment. Results: Diabetes led to increase vessel leakage, pericyte loss and VEGF protein level in the mouse retinas compared with controls; however, these changes were effectively blocked by resveratrol treatment. Conclusion: Our data suggest that resveratrol is effective to decrease vascular lesions and VEGF induction in mouse retinas of early diabetes.
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