治疗老年性黄斑变性的天然产物:线粒体质量控制和cGAS/STING通路的新见解

IF 8.9
Journal of pharmaceutical analysis Pub Date : 2025-05-01 Epub Date: 2024-11-16 DOI:10.1016/j.jpha.2024.101145
Xuelu Xie, Shan Lian, Wenyong Yang, Sheng He, Jingqiu He, Yuke Wang, Yan Zeng, Fang Lu, Jingwen Jiang
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引用次数: 0

摘要

年龄相关性黄斑变性(AMD)是一种影响全球老年人视力的疾病。虽然目前的治疗方法已经显示出对AMD的有效性,但一些患者可能仍然没有反应并继续经历疾病进展。因此,迫切需要深入了解AMD的发病机制,以确定AMD治疗的潜在药物靶点。最近有研究表明,线粒体功能障碍可导致活性氧(ROS)聚集,激活环GMP-AMP合成酶(cGAS)/干扰素基因刺激因子(STING)先天免疫通路,最终导致各种细胞(如心肌细胞和巨噬细胞)的无菌炎症和细胞死亡。因此,结合针对线粒体功能障碍和炎症介质的策略可能在促进AMD治疗方面具有很大的潜力。值得注意的是,新出现的证据表明,靶向线粒体质量控制(MQC)和cGAS/STING先天免疫途径的天然产物在治疗AMD方面表现出希望。在此,我们总结了可能直接或间接影响MQC和cGAS/STING先天免疫通路的植物化学物质及其相互关联的介质,这些介质具有减轻氧化应激和抑制过度炎症反应的潜力,从而希望为AMD的治疗干预提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural products for the treatment of age-related macular degeneration: New insights focusing on mitochondrial quality control and cGAS/STING pathway.

Age-related macular degeneration (AMD) is a disease that affects the vision of elderly individuals worldwide. Although current therapeutics have shown effectiveness against AMD, some patients may remain unresponsive and continue to experience disease progression. Therefore, in-depth knowledge of the mechanism underlying AMD pathogenesis is urgently required to identify potential drug targets for AMD treatment. Recently, studies have suggested that dysfunction of mitochondria can lead to the aggregation of reactive oxygen species (ROS) and activation of the cyclic GMP-AMP synthase (cGAS)/stimulator of interferon genes (STING) innate immunity pathways, ultimately resulting in sterile inflammation and cell death in various cells, such as cardiomyocytes and macrophages. Therefore, combining strategies targeting mitochondrial dysfunction and inflammatory mediators may hold great potential in facilitating AMD management. Notably, emerging evidence indicates that natural products targeting mitochondrial quality control (MQC) and the cGAS/STING innate immunity pathways exhibit promise in treating AMD. Here, we summarize phytochemicals that could directly or indirectly influence the MQC and the cGAS/STING innate immunity pathways, as well as their interconnected mediators, which have the potential to mitigate oxidative stress and suppress excessive inflammatory responses, thereby hoping to offer new insights into therapeutic interventions for AMD treatment.

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