Oral 8-aminoguanine against age-related retinal degeneration

Yuanyuan Chen, Abhishek Vats, Yibo Xi, Amanda Wolf-Johnston, Owen D. Clinger, Riley K. Arbuckle, Chase D. Dermond, Jonathan Li, Donna Stolze, J. Sahel, Edwin Jackson, Lori Birder
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Abstract

Abstract 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 Rho P23H/+ 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.
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口服 8-氨基鸟嘌呤防治老年性视网膜变性
摘要 老年人视力下降通常归因于视网膜老化,而视网膜老化容易导致视网膜组织发生病变,如老年性黄斑变性。目前,治疗视网膜变性的有效口服药物还很有限。我们利用老年 Fischer 344 大鼠模型,针对老年性视网膜变性提出了一种新型口服干预药物--8-氨基鸟嘌呤(8-AG)。从 22 个月大的大鼠开始,通过饮水摄入低剂量 8-AG (5 毫克/千克体重),持续 8 周,结果显示视网膜得到了显著的保护。具体表现为视网膜厚度增加、感光器完整性改善以及视网膜电图反应增强。8-AG 能有效减少与视网膜老化相关的细胞凋亡、氧化损伤和微胶质细胞/巨噬细胞活化。8-AG可部分缓解视网膜嘌呤代谢组中由年龄引起的变化,即肌苷、次黄嘌呤和黄嘌呤水平的升高。转录组学强调了 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 还在 Rho P23H/+ 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 定位为一种很有前景的抗视网膜老化口服药物。结合之前在不同疾病模型中的研究结果,8-AG 是一种很有前景的抗衰老化合物,能够逆转常见的衰老特征。
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