Ida Hisashi, Ishibashi Kazuki, Reiser Karen, Hjelmeland Leonard M, Handa James T
Department of Ophthalmology, UC Davis, California, USA.
Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2348-54. doi: 10.1167/iovs.03-1337.
Low-dose D-galactose treatment in mice induces accelerated aging due to advanced glycation endproduct (AGEs) formation. The purpose of this study was to identify ultrastructural aging in the retinal pigment epithelium (RPE)-Bruch's membrane-choriocapillaris.
Five-month-old C57Bl6 mice were injected daily with D-galactose or control buffer for 8 weeks. Eighteen-month-old mice were also treated with control buffer for 8 weeks. Eyes were prepared for electron microscopy and AGE-specific fluorescence at ex = 370 nm/em = 440 nm and ex = 330 nm/ex = 390 nm.
D-Galactose treatment induced AGE-specific fluorescence in lens and RPE/choroid compared to buffer-treated controls. In D-galactose-treated animals, the RPE had dilated and fewer basolateral infoldings. Bruch's membrane had alterations that included significant thickening, sub-RPE and prominent outer collagenous layer deposits, and choriocapillaris basement membrane duplication/splitting and thickening. The choriocapillaris endothelium displayed fenestration loss.
Ultrastructural aging to the RPE-Bruch's membrane-choriocapillaris developed in mice treated with low-dose D-galactose. These changes could contribute to age-related changes that promote early age-related disease.
小鼠低剂量D-半乳糖治疗会因晚期糖基化终产物(AGEs)形成而加速衰老。本研究的目的是确定视网膜色素上皮(RPE)-布鲁赫膜-脉络膜毛细血管的超微结构衰老情况。
对5月龄C57Bl6小鼠每天注射D-半乳糖或对照缓冲液,持续8周。对18月龄小鼠也用对照缓冲液处理8周。制备眼睛用于电子显微镜检查以及在激发波长ex = 370 nm/发射波长em = 440 nm和ex = 330 nm/ex = 390 nm下检测AGE特异性荧光。
与缓冲液处理的对照相比,D-半乳糖处理诱导晶状体和RPE/脉络膜出现AGE特异性荧光。在D-半乳糖处理的动物中,RPE扩张且基底外侧褶皱减少。布鲁赫膜出现改变,包括显著增厚、RPE下和突出的外层胶原层沉积,以及脉络膜毛细血管基底膜重复/分裂和增厚。脉络膜毛细血管内皮出现窗孔丧失。
低剂量D-半乳糖处理的小鼠出现了RPE-布鲁赫膜-脉络膜毛细血管的超微结构衰老。这些变化可能导致促进早期年龄相关性疾病的年龄相关变化。