Investigation of novel combination therapy for age-related macular degeneration on ARPE-19 cells

Madhuri Dandamudi, Peter Mcloughlin, G. Behl, Lee Coffey, Anuj Chauhan, David Kent, Sweta Rani, Laurence Fitzhenry
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Abstract

Age-related macular degeneration (AMD) is a multifactorial degenerative disease characterised by the gradual loss of central vision in individuals aged more than 50 years. There is currently no cure for this disease, but treatment can delay its progression. Consequently, there is an urgent need for the development of both new and cost-effective therapeutics. In this study, a novel combination of a corticosteroid and flavonoid was investigated on human retinal pigment epithelial cell lines to explore its potential pharmacological effect on AMD. Combination therapies, such as anti-VEGF (vascular endothelial growth factor) agents combined with photodynamic therapy and anti-VEGF agents in conjunction with corticosteroids, have been utilized previously and are known to be effective. However anti-VEGF injections are associated with serious side effects and are costly. Various disease conditions associated with AMD were stimulated on human retinal cells, which were then exposed to different concentrations of triamcinolone acetonide (TA) and quercetin (QCN) individually and in combination. This investigation aimed to assess their potential for the treatment of AMD. The combination of TA and QCN demonstrated a superior anti-inflammatory effect, as TA and QCN primarily act on different inflammatory signaling pathways. Furthermore, in terms of anti-VEGF activity, both drugs exert their effects through different mechanisms: QCN inhibits kinase pathways leading to the deactivation of VEGF receptors, whereas TA destabilises VEGF mRNA, resulting in increased suppression of VEGF-C with combination treatments. The anti-oxidant assay yielded similar outcomes, demonstrating a synergetic effect when treated with combination drugs. These findings collectively suggest TA and QCN as a promising combination therapy for targeting AMD with multiple pathological conditions.
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在 ARPE-19 细胞上研究治疗老年性黄斑变性的新型联合疗法
老年黄斑变性(AMD)是一种多因素退行性疾病,其特征是 50 岁以上的人逐渐丧失中心视力。这种疾病目前无法治愈,但治疗可以延缓其发展。因此,迫切需要开发新的、具有成本效益的治疗方法。本研究在人类视网膜色素上皮细胞系中研究了皮质类固醇和类黄酮的新型组合,以探索其对老年性视网膜病变的潜在药理作用。抗血管内皮生长因子(anti-VEGF)药物与光动力疗法相结合,以及抗血管内皮生长因子药物与皮质类固醇药物相结合等联合疗法以前就已使用过,而且效果显著。然而,注射抗血管内皮生长因子会产生严重的副作用,而且费用昂贵。研究人员对人类视网膜细胞进行了与老年性视网膜病变相关的各种疾病刺激,然后将其暴露于不同浓度的曲安奈德丙酮(TA)和槲皮素(QCN)的单独或组合中。这项研究旨在评估它们治疗老年性视网膜病变的潜力。由于TA和QCN主要作用于不同的炎症信号通路,因此TA和QCN的组合具有更优越的抗炎效果。此外,在抗血管内皮生长因子活性方面,这两种药物通过不同的机制产生作用:QCN 可抑制激酶通路,导致血管内皮生长因子受体失活,而 TA 则会破坏血管内皮生长因子 mRNA 的稳定性,从而在联合治疗时增加对血管内皮生长因子-C 的抑制。抗氧化试验也得出了类似的结果,表明联合用药可产生协同效应。这些发现共同表明,TA 和 QCN 是一种很有前景的联合疗法,可用于治疗具有多种病理条件的 AMD。
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