外层核层
感光细胞
氧化应激
视网膜变性
细胞凋亡
氧化损伤
DNA损伤
视网膜
内科学
化学
视网膜
视紫红质
内分泌学
氧化磷酸化
生物
分子生物学
受体
毒性
细胞
活性氧
半胱氨酸蛋白酶3
坏死
眼科
程序性细胞死亡
细胞损伤
作者
Mandy C. Kao,Wan-Ju Yeh,Hsin‐Yi Yang,Chih‐Hsiung Wu
出处
期刊:Antioxidants
[Multidisciplinary Digital Publishing Institute]
日期:2025-07-22
卷期号:14 (8): 898-898
标识
DOI:10.3390/antiox14080898
摘要
Retinal degeneration is associated with dietary factors and environmental light exposure. This study investigated the effects of a high-fructose high-fat (HFHF) diet on susceptibility to blue light (BL)-induced retinal damage. Male ICR mice were randomized into three groups: control, BL alone, and BL plus HFHF diet (BL + HFHF). The BL + HFHF group consumed the HFHF diet for 40 weeks, followed by 8 weeks of low-intensity BL exposure (465 nm, 37.7 lux, 0.8 μW/cm2) for 6 h daily. The BL group underwent the same BL exposure while kept on a standard diet. Histopathological analysis showed that, under BL exposure, the HFHF diet significantly reduced the number of photoreceptor nuclei and the thickness of the outer nuclear layer and inner/outer segments compared to the BL group (p < 0.05). While BL exposure alone caused oxidative DNA damage, rhodopsin loss, and Müller cell activation, the combination with an HFHF diet significantly amplified the oxidative DNA damage and Müller cell activation. Moreover, the HFHF diet increased blood–retinal barrier permeability and triggered apoptosis under BL exposure. Mechanistically, the BL + HFHF group exhibited increased retinal advanced glycated end product (AGE) deposition, accompanied by the activation of the receptor for AGE (RAGE), NFκB, and the NLRP3 inflammasome-dependent IL-1β pathway. In conclusion, this study underscores that unhealthy dietary factors, particularly those high in fructose and fat, may intensify the hazard of BL and adversely impact visual health.
科研通智能强力驱动
Strongly Powered by AbleSci AI