Department of Ophthalmology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, P.R. China.
PLoS One. 2012;7(12):e53329. doi: 10.1371/journal.pone.0053329. Epub 2012 Dec 28.
To investigate the effects of curcumin on the development of experimental choroidal neovascularization (CNV) with underlying cellular and molecular mechanisms.
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.
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).
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.
研究姜黄素对实验性脉络膜新生血管(CNV)形成的影响及其潜在的细胞和分子机制。
C57BL/6N 小鼠在激光诱导 CNV 前连续 3 天每天腹腔注射姜黄素预处理,直至研究结束时仍继续药物治疗。第 7 天和第 14 天通过视网膜色素上皮(RPE)-脉络膜平面铺片的荧光素标记葡聚糖血管造影术分析 CNV 面积,第 14 天激光光凝后通过荧光素血管造影术(FA)评估 CNV 渗漏。第 3 天通过免疫组织化学法在 RPE-脉络膜平面铺片上评估 F4/80 阳性巨噬细胞和 GR-1 阳性粒细胞的浸润情况。第 3 天通过实时 PCR(F4/80)和 Western 印迹(GR-1)定量分析 RPE-脉络膜复合体中的表达。第 3 天通过 ELISA 检测 RPE-脉络膜中血管内皮生长因子(VEGF)、肿瘤坏死因子(TNF)-α、单核细胞趋化蛋白(MCP)-1 和细胞间黏附分子(ICAM)-1 的水平。第 3 天在 CNV 病变的冷冻切片上进行 F4/80 和 VEGF 的双重免疫染色。通过 Western 印迹法测定 RPE-脉络膜中核因子(NF)-κB 和缺氧诱导因子(HIF)-1α的表达。
与对照组相比,姜黄素治疗组的 CNV 面积(P<0.05)和 CNV 渗漏(P<0.001)显著减少。姜黄素治疗导致 F4/80 阳性巨噬细胞(P<0.05)和 GR-1 阳性粒细胞浸润(P<0.05)显著抑制。VEGF 主要在激光损伤部位的 F4/80 阳性巨噬细胞中表达,姜黄素治疗可抑制其表达(P<0.01)。姜黄素抑制 RPE-脉络膜中 TNF-α(P<0.05)、MCP-1(P<0.05)和 ICAM-1(P<0.05)的水平,并抑制核提取物中 NF-κB 的激活(P<0.05)和 HIF-1α 的激活(P<0.05)。
姜黄素治疗可抑制 CNV 的发展,同时抑制 NF-κB 和 HIF-1α的激活、炎症和血管生成细胞因子的上调以及浸润的巨噬细胞和粒细胞,为姜黄素补充作为抑制年龄相关性黄斑变性(AMD)相关 CNV 的治疗策略提供了分子和细胞证据。