国际眼科纵览 ›› 2025, Vol. 49 ›› Issue (1): 19-24.doi: 10.3760/cma.j.cn115500-20241017-01004

• 综述 • 上一篇    下一篇

硒性白内障动物模型的研究进展

吴夕瑾 王震宇 方蕊 宋旭东   

  1. 首都医科大学附属北京同仁医院 北京同仁眼科中心 眼科学与视觉科学北京市重点实验,北京 100730
  • 收稿日期:2024-10-07 出版日期:2025-02-22 发布日期:2025-02-20
  • 通讯作者: 宋旭东,Email:drxdsong@sina.com
  • 基金资助:
    国家自然科学基金(82271067)

The progress of selenium-induced cataract 

Wu Xijin, Wang Zhenyu, Fang Rui, Song Xudong   

  1. Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University; Beijing  Key Laboratory of Ophthalmology & Visual Science,  Beijing 100730, China
  • Received:2024-10-07 Online:2025-02-22 Published:2025-02-20
  • Contact: Song Xudong, Email: drxdsong@sina.com
  • Supported by:
    National Natural Science Foundation of China (82271067)

摘要:

硒性白内障动物模型因其便捷、可重复性高等特点,被广泛应用于年龄相关性白内障的研究。硒性白内障体内动物模型可通过于大鼠皮下或腹腔注射亚硒酸钠溶液进行构建,将离体的大鼠晶状体置于含有高浓度亚硒酸钠的培养基中孵育可构建体外模型。亚硒酸钠可阻断晶状体上皮细胞细胞周期,加速其凋亡。此外,亚硒酸钠通过诱导晶状体内氧化应激反应,使过氧化氢酶及超氧化物歧化酶活性降低,丙二醛含量增加,还原型烟酰胺腺嘌呤二核苷酸磷酸浓度降低,改变晶状体细胞的代谢状态,使钙离子稳态失衡并激活钙蛋白酶,引发晶状体蛋白水解、相变,细胞骨架蛋白丢失,最终导致晶状体混浊。既往研究已证实,维生素C、钙蛋白酶抑制剂E64等可延缓硒性白内障进展,但应考虑亚硒酸钠对肝肾组织的氧化应激作用的影响。 (国际眼科纵览,2025, 49:19-24)

关键词: 硒, 白内障, 动物模型

Abstract: The selenium-induced cataract animal model is extensively utilized in investigating age-related cataracts due to its convenience and high reproducibility. In vivo models can be established by subcutaneous or intraperitoneal injection of sodium selenite solution into rats, while in vitro models can be created by incubating isolated rat lenses in a medium containing a high concentration of sodium selenite. Sodium selenite arrests lens epithelial cells in the cell cycle, accelerating apoptosis. Furthermore, it induces oxidative stress within the lens, reducing catalase and superoxide dismutase activities, increasing malondialdehyde levels, and decreasing nicotinamide adenine dinucleotide phosphate concentrations. These changes alter the metabolic state of lens cells, disrupt calcium ion homeostasis, and activate calpains, leading to proteolysis, phase transition of the lens, and loss of cytoskeletal proteins, ultimately resulting in lens opacification. Previous studies have confirmed that vitamin C and the calpain inhibitor E64 could delay the progression of selenium-induced cataracts; however, the effects of sodium selenite on oxidative stress in liver and kidney tissues should also be considered. (Int Rev Ophthalmol, 2025, 49:  19-24)

Key words: selenium, cataract, animal model