实验动物与比较医学 ›› 2026, Vol. 46 ›› Issue (5): 650-659.DOI: 10.12300/j.issn.1674-5817.2026.010

• 实验动物与中药学研究 • 上一篇    下一篇

护眼复合配方对蓝光损伤模型小鼠视网膜的功效评估

许浩莀, 乐卿清, 何西文, 蔡兵, 杨隆河()()   

  1. 自然资源部第三海洋研究所 海洋生物资源开发利用工程技术创新中心, 厦门 361005
  • 收稿日期:2026-01-08 修回日期:2026-06-16 出版日期:2026-10-25 发布日期:2026-10-16
  • 通讯作者: 杨隆河(1986—),男,博士,副研究员,研究方向:海洋药物药理及功能食品研究。E-mail:longheyang@tio.org.cn。ORCID: 0009-0006-6101-2066
  • 作者简介:
    许浩莀(1999—),男,硕士,研究方向:海洋功能食品研究。E-mail: 15739171206@163.com
  • 基金资助:
    海洋生物医药领域省科技计划定向项目“海藻寡糖降解菌株的适应性进化及功能食品开发应用”(2025Y0079)

Evaluation of the Efficacy of an Eye-Protective Compound Formula on the Retina in a Mouse Model of Blue Light-Induced Damage

XU Haochen, LE Qingqing, HE Xiwen, CAI Bing, YANG Longhe()()   

  1. Technical Innovation Center for Utilization of Marine Biological Resources, Third Institute of Oceanography, Ministry of Natural Resources, Xiamen 361005, China
  • Received:2026-01-08 Revised:2026-06-16 Published:2026-10-25 Online:2026-10-16
  • Correspondence to:
    YANG Longhe (ORCID: 0009-0006-6101-2066), E-mail:

摘要:

目的 为探明蓝光诱导小鼠视网膜损伤的时间依赖性,确立适宜的动物模型,并评价含叶黄素酯、DHA藻油、黑果枸杞等药食同源原料的复合配方对视网膜的保护作用。 方法 将56只SPF级雄性C57BL/6J小鼠中的32只随机分为对照组、模型组(1 h、3 h、6 h照射)(n=8),以确定蓝光最佳照射时间。首先采用467 nm发光二极管[(5 000±200) lx]蓝光分别照射小鼠1 h、3 h、6 h,然后分别用苏木精-伊红染色切片检测小鼠视网膜组织病理学改变及厚度,用试剂盒方法检测血清丙二醛(malondialdehyde,MDA)和谷胱甘肽(glutathione,GSH)水平,使用实时荧光定量反转录PCR检测视网膜炎症因子mRNA表达量。确定3 h为适宜模型后,其余24只小鼠用于护眼复合配方对蓝光视网膜损伤的干预实验,以复合配方(1 000 mg·kg⁻¹·d⁻¹)持续灌胃小鼠14 d,再行3 h蓝光照射,以同样的方法评估以上指标。 结果 随照射时间的延长,小鼠视网膜各层的厚度逐渐变薄(P<0.05至P<0.01),细胞排列紊乱;血清MDA含量逐步升高(P<0.01),而GSH含量逐步降低(P<0.01);视网膜组织白细胞介素-1β(interleukin-1β,IL-1β)、白细胞介素-6(interleukin-6,IL-6)和肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)的mRNA表达水平随着照射时间延长逐渐上调,其中1 h照射组指标变化较小(P>0.05),6 h照射组变化最显著(P<0.000 1),因此选择各项指标差异显著且适中的3 h(P<0.001)蓝光照射作为后续造模条件。护眼复合配方干预后,与模型组相比,小鼠血清MDA含量显著降低(P<0.01),而血清GSH含量显著升高(P<0.05);视网膜中炎症因子IL-1β(P<0.000 1)、IL-6(P<0.001)和TNF-α(P<0.01)表达量显著下调;视网膜总厚度显著增加(P<0.01),且内丛状层(P<0.05)、内核层(P<0.05)、外丛状层(P<0.05)与外核层(P<0.01)厚度均显著增加;组织病理学显示,其视网膜及细胞排列的规律性与致密程度均明显优于模型组。 结论 3 h特定照度的蓝光照射可建立稳定的小鼠视网膜损伤模型;护眼复合配方通过抗氧化-抗炎途径缓解损伤,为相关功能食品的开发提供实验依据。

关键词: 叶黄素, 蓝光, 视网膜, 氧化应激, 炎症, 功能食品, C57BL/6J小鼠

Abstract:

Objective To investigate the time-dependent pattern of blue light-induced retinal damage in mice, establish a suitable animal model, and evaluate the protective effects of a compound formula containing lutein esters, DHA algal oil, Lycium ruthenicum, and other ingredients used as both food and medicine. Methods Thirty-two of the 56 SPF-grade male C57BL/6J mice were randomly divided into a control group and model groups (1 h, 3 h, and 6 h irradiation) (n=8 per group) to determine the optimal blue light irradiation time. First, mice were exposed to blue light from a 467 nm light-emitting diode at (5 000±200) lx for 1 h, 3 h, and 6 h, respectively. Retinal histopathology and thickness were examined using hematoxylin‑eosin (HE) staining. Serum malondialdehyde (MDA) and glutathione (GSH) levels were measured using assay kits. Retinal inflammatory cytokine mRNA expression was assessed by real-time fluorescent quantitative reverse transcription PCR. After 3 h of blue light exposure was confirmed as the appropriate modeling condition, the remaining 24 mice were used in an intervention experiment to evaluate the protective effect of the eye-protective compound formula on blue light-induced retinal damage. The mice were administered the compound formula (1 000 mg·kg-1·d-1) by gavage for 14 days, followed by 3 h of blue light irradiation, and the same indicators were evaluated as described above. Results With prolonged irradiation time, the thickness of each retinal layer gradually decreased (P<0.05 to P<0.01) and cell arrangement became disordered. Serum MDA levels progressively increased (P<0.01), while GSH levels gradually decreased (P<0.01). The mRNA expression of interleukin-1β (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) in retinal tissue was significantly upregulated with increasing irradiation time. The 1 h irradiation group showed only minor changes (P>0.05), whereas the 6 h irradiation group exhibited the most pronounced changes (P<0.000 1). Therefore, 3 h of blue light irradiation (P<0.001), which showed significant yet moderate differences in all indicators, was selected as the subsequent modeling condition. After intervention with the eye-protective compound formula, compared with the model group, serum MDA level was significantly reduced (P<0.01), and serum GSH level was significantly increased (P<0.05). The expression levels of retinal inflammatory cytokines IL-1β (P<0.000 1), IL-6 (P<0.001), and TNF-α (P<0.01) were significantly downregulated. Total retinal thickness (P<0.01), as well as the thicknesses of the inner plexiform layer (P<0.05), inner nuclear layer (P<0.05), outer plexiform layer (P<0.05), and outer nuclear layer (P<0.01), were significantly increased compared with the model group. Histopathological examination also showed that the regularity and density of retinal cell arrangement were markedly better than those in the model group. Conclusion Blue light irradiation at a specific illuminance for 3 h can establish a stable mouse model of retinal damage. The compound formula alleviates retinal damage through antioxidant and anti-inflammatory pathways, providing an experimental basis for the development of related functional foods.

Key words: Lutein, Blue light, Retina, Oxidative stress, Inflammation, Functional food, C57BL/6J mice

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