Liu Jingting, Jiang Enying, Kim Hyunjee, Moon Jayoung, Yoon Hyeon Jeong, Yoon Kyung Chul
Department of Ophthalmology, Chonnam National University Hospital, Dong-Gu, Republic of Korea.
J Ocul Pharmacol Ther. 2025 Aug;41(6):314-321. doi: 10.1089/jop.2024.0208. Epub 2025 Apr 28.
We evaluated the capacity of rebamipide (REB) to alleviate corneal epithelial damage induced via blue light (BL) exposure. Eight-week-old C57BL/6 mice were exposed to BL (410 nm, 100 J) twice daily for 10 days. The mice were randomly divided into 5 groups: 1 untreated and 4 groups receiving BL exposure ± different topical treatments: BL exposure alone, carboxymethylcellulose, 5% -acetylcysteine, and REB. Reactive oxygen species (ROS) levels were assessed, and -associated X protein ( was analyzed. Apoptotic cells were detected, inflammatory cytokine levels [tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6)] were measured using enzyme-linked immunosorbent assay (ELISA), and histopathological changes in the cornea were evaluated using hematoxylin and eosin (H&E) staining. The REB group demonstrated significantly lower BL exposure-induced ROS levels ( < 0.01) and expression ( < 0.01) than the BL group. The number of Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) positive cells were lower in the REB group than in the BL group ( < 0.01). Furthermore, ELISA analysis revealed significantly reduced TNF-α and IL-6 levels in the REB group relative to BL group levels ( < 0.01). Hematoxylin and eosin staining showed preservation of corneal epithelial thickness. Rebamipide alleviated BL-induced oxidative damage to ocular surfaces by reducing ROS levels, inhibiting apoptosis, and suppressing inflammatory cytokine expression.
我们评估了瑞巴派特(REB)减轻蓝光(BL)照射所致角膜上皮损伤的能力。8周龄的C57BL/6小鼠每天接受两次BL(410 nm,100 J)照射,持续10天。小鼠被随机分为5组:1组未处理,4组接受BL照射并给予不同的局部治疗:单独BL照射、羧甲基纤维素、5%乙酰半胱氨酸和REB。评估活性氧(ROS)水平,并分析相关X蛋白( )。检测凋亡细胞,使用酶联免疫吸附测定(ELISA)测量炎性细胞因子水平[肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)],并使用苏木精和伊红(H&E)染色评估角膜的组织病理学变化。与BL组相比,REB组显示出BL照射诱导的ROS水平显著降低(<0.01)和 表达显著降低(<0.01)。REB组中末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)阳性细胞数量低于BL组(<0.01)。此外,ELISA分析显示,相对于BL组水平,REB组中TNF-α和IL-6水平显著降低(<0.01)。苏木精和伊红染色显示角膜上皮厚度得以保留。瑞巴派特通过降低ROS水平、抑制细胞凋亡和抑制炎性细胞因子表达,减轻了BL诱导的眼表氧化损伤。