Department of Ophthalmology, Kanazawa Medical University, Kahoku, Japan.
Department of Pharmacology, Kanazawa Medical University, Kahoku, Japan.
J Ocul Pharmacol Ther. 2024 Sep;40(7):428-434. doi: 10.1089/jop.2024.0025.
This study aimed to investigate the relationship between diclofenac sodium ophthalmic solution (DFNa) and corneal epithelial cell damage and to evaluate the preventive effect of rebamipide (RBM) on it. DFNa, DFNa/preservative-free (PF), or 0.5% chlorobutanol (CB) solution was instilled into the conjunctival sac of a normal rabbit eye, and corneal resistance measurement (using a corneal resistance device [CRD]) was performed 120 min after the end of instillation. Then, fluorescent staining (FL), corneal tissue staining (hematoxylin and eosin [H&E]), and immunostaining (zona occlusion-1) were performed (RBM-untreated group). However, RBM was instilled into the eyes of another group of normal rabbits, followed by each of the solutions; 120 min after the end of instillation, all evaluations were performed for this group (RBM treatment group). Using the CRD method, in the RBM-untreated group, corneal resistance (CR; %) was found to be significantly reduced in DFNa (79.9 ± 19.4%), DFNa/PF (89.1 ± 17.3%), and 0.5% CB (83.8 ± 10.6%). In addition, DFNa and 0.5% CB solutions showed positive staining in the FL staining method. In the H&E staining method, some clear voids were observed in the outermost layer of the cornea using DFNa and 0.5% CB solutions. However, corneal epithelial damage was suppressed in the RBM treatment group. ZO-1 immunostaining in DFNa and 0.5% CB solutions revealed discontinuous localization of ZO-1 at the cell periphery. RBM eye drops were effective in preventing corneal epithelial damage caused by DFNa eye drops, and CB was considered to be the main causative agent of this damage.
本研究旨在探讨双氯芬酸钠滴眼液(DFNa)与角膜上皮细胞损伤的关系,并评价瑞巴派特(RBM)对此的预防作用。将 DFNa、DFNa/无防腐剂(PF)或 0.5%氯丁醇(CB)溶液滴入正常兔眼的结膜囊中,滴注结束后 120 分钟进行角膜电阻测量(使用角膜电阻仪[CRD])。然后,进行荧光染色(FL)、角膜组织染色(苏木精和伊红[H&E])和免疫染色(区带闭塞-1)(RBM 未处理组)。然而,将 RBM 滴入另一组正常兔眼,然后滴注每种溶液;滴注结束后 120 分钟,对该组进行所有评估(RBM 治疗组)。使用 CRD 方法,在 RBM 未处理组中,DFNa(79.9±19.4%)、DFNa/PF(89.1±17.3%)和 0.5%CB(83.8±10.6%)的角膜阻力(CR;%)明显降低。此外,DFNa 和 0.5%CB 溶液在 FL 染色法中呈阳性染色。在 H&E 染色法中,DFNa 和 0.5%CB 溶液在外层角膜中观察到一些清晰的空洞。然而,在 RBM 治疗组中,角膜上皮损伤得到抑制。DFNa 和 0.5%CB 溶液中的 ZO-1 免疫染色显示 ZO-1 在细胞边缘的连续性定位中断。RBM 滴眼液可有效预防 DFNa 滴眼液引起的角膜上皮损伤,CB 被认为是造成这种损伤的主要原因。