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瑞巴派特滴眼液对蓝光诱导的眼表氧化损伤的有益作用。

Beneficial Effect of Rebamipide Eye Drops on Blue Light-Induced Oxidative Damage in the Ocular Surface.

作者信息

Liu Jingting, Jiang Enying, Kim Hyunjee, Moon Jayoung, Yoon Hyeon Jeong, Yoon Kyung Chul

机构信息

Department of Ophthalmology, Chonnam National University Hospital, Dong-Gu, Republic of Korea.

出版信息

J Ocul Pharmacol Ther. 2025 Aug;41(6):314-321. doi: 10.1089/jop.2024.0208. Epub 2025 Apr 28.

DOI:10.1089/jop.2024.0208
PMID:40293740
Abstract

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.

摘要

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。

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