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莪术呋喃酮,一种来自温郁金的独特倍半萜,具有抗血管生成活性,并能减轻缺血诱导的视网膜新生血管形成。

Curcumolide, a unique sesquiterpenoid from Curcuma wenyujin displays anti-angiogenic activity and attenuates ischemia-induced retinal neovascularization.

机构信息

Pharmacy School, Wenzhou Medical University, A509, Pharmacy School Building, Wenzhou, Zhejiang Province 325035, PR China.

Pharmacy School, Wenzhou Medical University, A509, Pharmacy School Building, Wenzhou, Zhejiang Province 325035, PR China.

出版信息

Phytomedicine. 2019 Nov;64:152923. doi: 10.1016/j.phymed.2019.152923. Epub 2019 Apr 12.

Abstract

BACKGROUND

Targeting vascular endothelial growth factor is a common treatment strategy for neovascular eye disease, a leading cause of visual impairment and blindness. However, these approaches are limited or carry various complications. Therefore, there is an urgent need for the development of unique therapeutic approaches.

PURPOSE

To investigate the anti-angiogenic effects of curcumolide and its mechanism of action.

METHODS /STUDY DESIGNS: In this study, we examine the effects of curcumolide on the process of vasculature formation, including cell proliferation, migration, tube formation and apoptosis in vitro using human umbilical vascular endothelial cells (HUVECs). We also assess the anti-angiogenic effects of curcumolide in vivo using a mouse model of oxygen induced retinopathy (OIR). The mechanism of anti-angiogenic effects was investigated by measuring the expression level of various signaling proteins and the molecular docking simulations.

RESULTS

Intravitreal injection of curcumolide reduced the formation of retinal neovascular tufts and VEGFR2 phosphorylation in the murine OIR model at concentrations administered without definite cellular and retinal toxicities. Curcumolide suppressed VEGF-induced HRMECs proliferation, migration and tube formation in a dose-dependent manner. Meanwhile, it promoted caspase-dependent apoptosis. Curcumolide also inhibited VEGF-induced phosphorylation of VEGFR-2 tyrosine kinase, and suppressed downstream protein kinases of VEGFR2, including Src, FAK, ERK, AKT, and mTOR in HRMECs. In silico study revealed that curcumolide bound with ATP-binding sites of the VEGFR2 kinase unit by the formation of a hydrogen bond and hydrophobic interactions.

CONCLUSION

Curcumolide has anti-angiogenic activity in HUVECs and in a murine OIR model of ischemia-induced retinal neovascularization, and it might be a potential drug candidate for the treatment of proliferative diabetic retinopathy.

摘要

背景

针对血管内皮生长因子是治疗新生血管性眼病的常见策略,新生血管性眼病是视力损害和失明的主要原因。然而,这些方法存在局限性或伴有各种并发症。因此,迫切需要开发独特的治疗方法。

目的

研究莪术呋喃二酮的抗血管生成作用及其作用机制。

方法/研究设计:在这项研究中,我们使用人脐静脉内皮细胞(HUVEC)研究莪术呋喃二酮对血管形成过程的影响,包括细胞增殖、迁移、管形成和凋亡。我们还使用氧诱导视网膜病变(OIR)小鼠模型评估莪术呋喃二酮的抗血管生成作用。通过测量各种信号蛋白的表达水平和分子对接模拟来研究抗血管生成作用的机制。

结果

在浓度下,玻璃体内注射莪术呋喃二酮可减少 OIR 模型中小鼠视网膜新生血管丛的形成和 VEGFR2 磷酸化,而不会产生明确的细胞和视网膜毒性。莪术呋喃二酮以剂量依赖性方式抑制 VEGF 诱导的 HRMECs 增殖、迁移和管形成。同时,它促进了 caspase 依赖性细胞凋亡。莪术呋喃二酮还抑制了 VEGF 诱导的 VEGFR-2 酪氨酸激酶磷酸化,并抑制了 VEGFR2 的下游蛋白激酶,包括 HRMECs 中的Src、FAK、ERK、AKT 和 mTOR。计算研究表明,莪术呋喃二酮通过形成氢键和疏水相互作用与 VEGFR2 激酶单元的 ATP 结合位点结合。

结论

莪术呋喃二酮在 HUVECs 中和缺血性视网膜新生血管形成的 OIR 小鼠模型中具有抗血管生成活性,可能是治疗增生性糖尿病视网膜病变的潜在候选药物。

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