Oral 8-aminoguanine against age-related retinal degeneration.
Yuanyuan ChenAbhishek VatsYibo XiAmanda Wolf-JohnstonOwen ClingerRiley ArbuckleChase DermondJonathan LiDonna StolzeJosé Alain SahelEdwin JacksonLori BirderPublished in: Research square (2024)
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.
Keyphrases
- optical coherence tomography
- diabetic retinopathy
- quantum dots
- optic nerve
- immune response
- low dose
- drinking water
- highly efficient
- mouse model
- visible light
- inflammatory response
- single cell
- high dose
- age related macular degeneration
- metabolic syndrome
- drug induced
- cell proliferation
- endoplasmic reticulum stress
- gestational age
- preterm birth
- cancer therapy