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Suppression of Experimental Choroidal Neovascularization by Curcumin in Mice
Author(s) -
Ping Xie,
Weiwei Zhang,
Songtao Yuan,
Zhiqiang Chen,
Qin Yang,
Dongqing Yuan,
Feng Wang,
Qinghuai Liu
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0053329
Subject(s) - choroidal neovascularization , vascular endothelial growth factor , choroid , immunostaining , curcumin , medicine , pathology , blot , fluorescein angiography , andrology , retinal , immunohistochemistry , chemistry , biology , retina , pharmacology , ophthalmology , biochemistry , neuroscience , gene , vegf receptors
Purpose To investigate the effects of curcumin on the development of experimental choroidal neovascularization (CNV) with underlying cellular and molecular mechanisms. Methods C57BL/6N mice were pretreated with intraperitoneal injections of curcumin daily for 3 days prior to laser-induced CNV, and the drug treatments were continued until the end of the study. The CNV area was analyzed by fluorescein-labeled dextran angiography of retinal pigment epithelium (RPE)-choroid flat mounts on day 7 and 14, and CNV leakage was evaluated by fluorescein angiography (FA) on day 14 after laser photocoagulation. The infiltration of F4/80 positive macrophages and GR-1 positive granulocytes were evaluated by immunohistochemistry on RPE-choroid flat mounts on day 3. Their expression in RPE-choroid complex was quantified by real-time PCR (F4/80) and Western blotting (GR-1) on day 3. RPE-choroid levels of vascular endothelial growth factor (VEGF), tumor necrosis factor (TNF)-α, monocyte chemotactic protein (MCP)-1, and intercellular adhesion molecule (ICAM)-1 were examined by ELISA on day 3. Double immunostaining of F4/80 and VEGF was performed on cryo-sections of CNV lesions on day 3. The expression of nuclear factor (NF)-κB and hypoxia-inducible factor (HIF)−1α in the RPE-choroid was determined by Western blotting. Results Curcumin-treated mice had significantly less CNV area ( P <0.05) and CNV leakage ( P <0.001) than vehicle-treated mice. Curcumin treatment led to significant inhibition of F4/80 positive macrophages ( P <0.05) and GR-1 positive granulocytes infiltration ( P <0.05). VEGF mainly expressed in F4/80 positive macrophages in laser injury sites, which was suppressed by curcumin treatment ( P <0.01). Curcumin inhibited the RPE-choroid levels of TNF-α ( P <0.05), MCP-1 ( P <0.05) and ICAM-1 ( P <0.05), and suppressed the activation of NF-κB in nuclear extracts ( P <0.05) and the activation of HIF−1α ( P <0.05). Conclusion Curcumin treatment led to the suppression of CNV development together with inflammatory and angiogenic processes including NF-κB and HIF−1α activation, the up-regulation of inflammatory and angiogenic cytokines, and infiltrating macrophages and granulocytes. This provides molecular and cellular evidence of the validity of curcumin supplementation as a therapeutic strategy for the suppression of age-related macular degeneration (AMD)-associated CNV.

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