Yanai Ryoji, Yasunaga Genta, Tsuji Shunya, Honda Takeshi, Iwata Arihiro, Miyagawa Eiji, Yoshida Koji, Kishimoto Mitsuhiro, Sakai Hiroki, Fujise Yoshihiro, Asagiri Masataka, Mitamura Yoshinori
Department of Ophthalmology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Institute of Cetacean Research, Chuo-ku, Tokyo, Japan.
FASEB J. 2025 Feb 28;39(4):e70378. doi: 10.1096/fj.202402041R.
Age-related macular degeneration (AMD) is a leading cause of blindness in Western and developing countries. Since antivascular endothelial growth factor (VEGF) therapy is available for the regression of choroidal neovascularization (CNV), it does not work for the pathophysiology of AMD so a cure is increasingly demanded. Whale oil promotes various bodily functions, such as anti-inflammatory effects for cardiovascular disease, but its physiological mechanisms are still unclarified. Here, we examined the effects of whale oil on a mouse model of AMD. The area of CNV measured in choroidal flat-mount preparations at 7 days after laser photocoagulation was significantly smaller in mice fed whale oil compared with control mice free of ω-3 long-chain polyunsaturated fatty acids (LCPUFAs). The plasma concentrations of ω-3 LCPUFAs were higher, whereas those of ω-6 LCPUFAs were lower in mice fed the diet containing whale oil than in those fed the control diet. The concentrations of various inflammatory cytokines and chemokines in the retina or choroid at 3 or 7 days after CNV induction differed between the two groups of mice. Furthermore, the concentration of VEGF was decreased in the retina but increased in the choroid at 7 or 3 days after photocoagulation, respectively. Our results thus show that dietary intake of whale oil-containing ω-3 LCPUFAs attenuated CNV in association with changes in inflammatory mediator levels and VEGF expression in the retina and choroid of mice, and it, therefore, warrants further study as a means to protect against AMD in humans.
年龄相关性黄斑变性(AMD)是西方国家和发展中国家失明的主要原因。由于抗血管内皮生长因子(VEGF)疗法可用于使脉络膜新生血管(CNV)消退,但它对AMD的病理生理学不起作用,因此人们对治愈方法的需求日益增加。鲸油可促进多种身体功能,如对心血管疾病的抗炎作用,但其生理机制仍不清楚。在此,我们研究了鲸油对AMD小鼠模型的影响。与不含ω-3长链多不饱和脂肪酸(LCPUFAs)的对照小鼠相比,喂食鲸油的小鼠在激光光凝后7天,脉络膜平铺制剂中测量的CNV面积明显更小。喂食含鲸油饮食的小鼠血浆中ω-3 LCPUFAs浓度较高,而ω-6 LCPUFAs浓度低于喂食对照饮食的小鼠。两组小鼠在诱导CNV后3天或7天,视网膜或脉络膜中各种炎性细胞因子和趋化因子的浓度有所不同。此外,光凝后7天或3天,视网膜中VEGF浓度降低,而脉络膜中VEGF浓度升高。因此,我们的结果表明,饮食摄入含鲸油的ω-3 LCPUFAs可减轻小鼠视网膜和脉络膜中炎性介质水平和VEGF表达的变化,从而减轻CNV,因此,作为预防人类AMD的一种手段,值得进一步研究。