Sulaiman Rania S, Merrigan Stephanie, Quigley Judith, Qi Xiaoping, Lee Bit, Boulton Michael E, Kennedy Breandán, Seo Seung-Yong, Corson Timothy W
Eugene and Marilyn Glick Eye Institute, Department of Ophthalmology, Indiana University School of Medicine, Indianapolis, Indiana 46202, United States of America.
Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, Indiana 46202, United States of America.
Sci Rep. 2016 May 5;6:25509. doi: 10.1038/srep25509.
Ocular neovascularisation underlies blinding eye diseases such as retinopathy of prematurity, proliferative diabetic retinopathy, and wet age-related macular degeneration. These diseases cause irreversible vision loss, and provide a significant health and economic burden. Biologics targeting vascular endothelial growth factor (VEGF) are the major approach for treatment. However, up to 30% of patients are non-responsive to these drugs and they are associated with ocular and systemic side effects. Therefore, there is a need for small molecule ocular angiogenesis inhibitors to complement existing therapies. We examined the safety and therapeutic potential of SH-11037, a synthetic derivative of the antiangiogenic homoisoflavonoid cremastranone, in models of ocular neovascularisation. SH-11037 dose-dependently suppressed angiogenesis in the choroidal sprouting assay ex vivo and inhibited ocular developmental angiogenesis in zebrafish larvae. Additionally, intravitreal SH-11037 (1 μM) significantly reduced choroidal neovascularisation (CNV) lesion volume in the laser-induced CNV mouse model, comparable to an anti-VEGF antibody. Moreover, SH-11037 synergised with anti-VEGF treatments in vitro and in vivo. Up to 100 μM SH-11037 was not associated with signs of ocular toxicity and did not interfere with retinal function or pre-existing retinal vasculature. SH-11037 is thus a safe and effective treatment for murine ocular neovascularisation, worthy of further mechanistic and pharmacokinetic evaluation.
眼部新生血管形成是导致失明性眼病的基础,如早产儿视网膜病变、增殖性糖尿病视网膜病变和湿性年龄相关性黄斑变性。这些疾病会导致不可逆的视力丧失,并带来重大的健康和经济负担。靶向血管内皮生长因子(VEGF)的生物制剂是主要的治疗方法。然而,高达30%的患者对这些药物无反应,并且它们与眼部和全身副作用相关。因此,需要小分子眼部血管生成抑制剂来补充现有疗法。我们在眼部新生血管形成模型中研究了抗血管生成高异黄酮cremastranone的合成衍生物SH-11037的安全性和治疗潜力。SH-11037在体外脉络膜芽生试验中剂量依赖性地抑制血管生成,并在斑马鱼幼虫中抑制眼部发育血管生成。此外,玻璃体内注射SH-11037(1μM)在激光诱导的脉络膜新生血管(CNV)小鼠模型中显著降低了CNV病变体积,与抗VEGF抗体相当。此外,SH-11037在体外和体内与抗VEGF治疗协同作用。高达100μM的SH-11037未出现眼部毒性迹象,也未干扰视网膜功能或现有的视网膜血管系统。因此,SH-11037是一种治疗小鼠眼部新生血管形成的安全有效的药物,值得进一步进行机制和药代动力学评估。