Kao Meng-Wei, Yeh Wan-Ju, Yang Hsin-Yi, Wu Chi-Hao
Graduate Program of Nutrition Science, School of Life Science, National Taiwan Normal University, Taipei 11677, Taiwan.
Department of Nutritional Science, Fu Jen Catholic University, New Taipei City 24205, Taiwan.
Antioxidants (Basel). 2025 Jul 22;14(8):898. doi: 10.3390/antiox14080898.
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/cm) 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 ( < 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.
视网膜变性与饮食因素和环境光照暴露有关。本研究调查了高糖高脂(HFHF)饮食对蓝光(BL)诱导的视网膜损伤易感性的影响。雄性ICR小鼠被随机分为三组:对照组、单纯蓝光组和蓝光加HFHF饮食组(BL + HFHF)。BL + HFHF组食用HFHF饮食40周,随后每天进行6小时的低强度蓝光暴露(465纳米,37.7勒克斯,0.8微瓦/平方厘米),持续8周。蓝光组在保持标准饮食的同时接受相同的蓝光暴露。组织病理学分析表明,在蓝光暴露下,与蓝光组相比,HFHF饮食显著减少了光感受器细胞核的数量以及外核层和内/外节的厚度(<0.05)。虽然单独的蓝光暴露会导致氧化性DNA损伤、视紫红质丢失和Müller细胞活化,但与HFHF饮食联合使用会显著放大氧化性DNA损伤和Müller细胞活化。此外,HFHF饮食会增加血视网膜屏障通透性,并在蓝光暴露下引发细胞凋亡。从机制上讲,BL + HFHF组视网膜晚期糖基化终产物(AGE)沉积增加,同时伴有AGE受体(RAGE)、NFκB和NLRP3炎性小体依赖性IL-1β途径的激活。总之,本研究强调不健康的饮食因素,尤其是那些高糖高脂的因素,可能会加剧蓝光的危害并对视觉健康产生不利影响。