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通过抑制内皮型一氧化氮合酶(eNOS)途径,卡伐他汀和阿柏西普协同抑制脉络膜新生血管形成。

Synergistic Suppression of Choroidal Neovascularization by Cavtratin and Aflibercept via Inhibition of the eNOS Pathway.

作者信息

Dong Yue, Li Yanlin, Zhou Xuan, Huang Wei, Yang Shasha, Lin Huishan, Wei Kun, Yao Jingwei, Zuo Haoyu, Zuo Chengguo

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology Visual Science, Guangzhou, China.

Guangzhou University of Chinese Medicine, Guangzhou, China.

出版信息

Curr Eye Res. 2025 Oct;50(10):1054-1063. doi: 10.1080/02713683.2025.2523916. Epub 2025 Aug 3.

Abstract

PURPOSE

Choroidal neovascularization (CNV) is a key pathological feature of exudative age-related macular degeneration (AMD), leading to severe vision loss. Despite anti-vascular endothelial growth factor (anti-VEGF) therapies being the first-line treatment for neovascularization, their long-term application faces challenges including treatment insensitivity and drug resistance. This study aims to investigate the role of Caveolin-1 (Cav-1) in CNV pathogenesis and evaluate the therapeutic potential of Cavtratin, a Cav-1 scaffolding domain-targeting peptide, alone and in combination with Aflibercept.

METHODS

A laser-induced CNV model in aged mice and VEGF-stimulated human umbilical vein endothelial cells (HUVECs) were used to assess Cav-1 expression dynamics and its interaction with endothelial nitric oxide synthase (eNOS). The effects of Cavtratin on angiogenesis were evaluated using tube formation assays, choroidal sprouting assays, and fluorescein angiography. Western blot and immunofluorescence staining were employed to analyze changes in molecular expression, localization, and inflammatory responses. The efficacy of Cavtratin-Aflibercept combination therapy was examined.

RESULTS

Cav-1 and eNOS were significantly upregulated during CNV progression ( < 0.001). Cavtratin effectively inhibited tube formation in HUVECs, suppressed choroidal sprouting , and reduced CNV leakage ( < 0.01). Mechanistically, Cavtratin suppressed eNOS phosphorylation and enhanced the anti-angiogenic effects of Aflibercept ( < 0.001). The combination therapy led to greater CNV inhibition, reduced inflammation, and allowed for a lower Aflibercept dosage while maintaining therapeutic efficacy.

CONCLUSION

Cavtratin combined with Aflibercept can effectively enhance anti-angiogenic efficacy and reduce inflammatory responses. Targeting the Cav-1/eNOS axis with Cavtratin provides a novel strategy to complement the limitations of anti-VEGF therapy. The synergistic effects of Cavtratin and Aflibercept suggest a promising approach to overcoming treatment resistance and improving clinical outcomes in CNV management.

摘要

目的

脉络膜新生血管(CNV)是渗出性年龄相关性黄斑变性(AMD)的关键病理特征,可导致严重视力丧失。尽管抗血管内皮生长因子(抗VEGF)疗法是新生血管形成的一线治疗方法,但其长期应用面临包括治疗不敏感和耐药性在内的挑战。本研究旨在探讨小窝蛋白-1(Cav-1)在CNV发病机制中的作用,并评估Cavtratin(一种靶向Cav-1支架结构域的肽)单独及与阿柏西普联合使用的治疗潜力。

方法

使用老年小鼠激光诱导的CNV模型和VEGF刺激的人脐静脉内皮细胞(HUVECs)来评估Cav-1表达动态及其与内皮型一氧化氮合酶(eNOS)的相互作用。使用管形成试验、脉络膜发芽试验和荧光素血管造影评估Cavtratin对血管生成的影响。采用蛋白质免疫印迹法和免疫荧光染色分析分子表达、定位和炎症反应的变化。检测Cavtratin-阿柏西普联合治疗的疗效。

结果

在CNV进展过程中,Cav-1和eNOS显著上调(<0.001)。Cavtratin有效抑制HUVECs中的管形成,抑制脉络膜发芽,并减少CNV渗漏(<0.01)。机制上,Cavtratin抑制eNOS磷酸化并增强阿柏西普的抗血管生成作用(<0.001)。联合治疗导致更大程度的CNV抑制,减轻炎症,并允许在维持治疗效果的同时降低阿柏西普剂量。

结论

Cavtratin与阿柏西普联合可有效增强抗血管生成疗效并减少炎症反应。用Cavtratin靶向Cav-1/eNOS轴提供了一种新策略,以弥补抗VEGF治疗的局限性。Cavtratin和阿柏西普的协同作用提示了一种有前景的方法,可克服治疗耐药性并改善CNV管理中的临床结果。

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