Chen Yuanyuan, Vats Abhishek, Xi Yibo, Wolf-Johnston Amanda, Clinger Owen, Arbuckle Riley, Dermond Chase, Li Jonathan, Stolze Donna, Sahel José-Alain, Jackson Edwin, Birder Lori
University of Pittsburgh.
University of Pittsburgh School of Medicine.
Res Sq. 2024 May 6:rs.3.rs-4022389. doi: 10.21203/rs.3.rs-4022389/v1.
Visual decline in the elderly is often attributed to retinal aging, which predisposes the tissue to pathologies such as age-related macular degeneration. Currently, effective oral pharmacological interventions for retinal degeneration are limited. We present a novel oral intervention, 8-aminoguanine (8-AG), targeting age-related retinal degeneration, utilizing the aged Fischer 344 rat model. A low-dose 8-AG regimen (5 mg/kg body weight) via drinking water, beginning at 22 months for 8 weeks, demonstrated significant retinal preservation. This was evidenced by increased retinal thickness, improved photoreceptor integrity, and enhanced electroretinogram responses. 8-AG effectively reduced apoptosis, oxidative damage, and microglial/macrophage activation associated with aging retinae. Age-induced alterations in the retinal purine metabolome, characterized by elevated levels of inosine, hypoxanthine, and xanthine, were partially mitigated by 8-AG. Transcriptomics highlighted 8-AG's anti-inflammatory effects on innate and adaptive immune responses. Extended treatment to 17 weeks further amplified the retinal protective effects. Moreover, 8-AG showed temporary protective effects in the mouse model of retinitis pigmentosa, reducing active microglia/macrophages. Our study positions 8-AG as a promising oral agent against retinal aging. Coupled with previous findings in diverse disease models, 8-AG emerges as a promising anti-aging compound with the capability to reverse common aging hallmarks.
老年人的视力下降通常归因于视网膜老化,这使该组织易患诸如年龄相关性黄斑变性等疾病。目前,针对视网膜变性的有效口服药物干预措施有限。我们利用老年Fischer 344大鼠模型,提出了一种针对年龄相关性视网膜变性的新型口服干预措施——8-氨基鸟嘌呤(8-AG)。从22个月开始,通过饮用水给予低剂量8-AG方案(5毫克/千克体重),持续8周,结果显示视网膜得到了显著保护。这表现为视网膜厚度增加、光感受器完整性改善以及视网膜电图反应增强。8-AG有效减少了与衰老视网膜相关的细胞凋亡、氧化损伤以及小胶质细胞/巨噬细胞激活。8-AG部分缓解了年龄诱导的视网膜嘌呤代谢组变化,其特征是肌苷、次黄嘌呤和黄嘌呤水平升高。转录组学突出了8-AG对先天性和适应性免疫反应的抗炎作用。延长治疗至17周进一步增强了视网膜保护作用。此外,8-AG在视网膜色素变性小鼠模型中显示出暂时的保护作用,减少了活跃的小胶质细胞/巨噬细胞。我们的研究将8-AG定位为一种有前景的抗视网膜老化口服药物。结合之前在多种疾病模型中的研究结果,8-AG成为一种有前景的抗衰老化合物,具有逆转常见衰老特征的能力。