# Comparison of the Therapeutic Effects of Rebamipide and Diquafosol on Apoptotic Damage of the Ocular Surface in Dry Eyes

**Authors:** Enying Jiang, Hui Jin, Jingting Liu, Hyun Jee Kim, Hee Su Yoon, Ji Suk Choi, Jayoung Moon, Hoon-In Choi, Hyeon-Jeong Yoon, Kyung Chul Yoon

PMC · DOI: 10.3390/antiox14070780 · Antioxidants · 2025-06-25

## TL;DR

This study compares two drugs, rebamipide and diquafosol, for their ability to protect eye cells from damage in dry eye disease.

## Contribution

The study reveals that rebamipide is more effective than diquafosol in reducing oxidative stress and cell death in dry eye disease.

## Key findings

- Rebamipide improved cell survival and reduced caspase-3 expression more effectively than diquafosol.
- Rebamipide showed better results in reducing ROS, lipid peroxidation, and apoptosis in a mouse model of dry eye.
- Rebamipide preserved corneal glycocalyx integrity and goblet cell density more effectively.

## Abstract

Dry eye disease (DED) is characterized by tear film instability and oxidative stress-induced epithelial damage. This study was conducted to compare the therapeutic effects of 2% rebamipide (REB) and 3% diquafosol (DQS) on oxidative stress-related apoptotic damage of the ocular surface in DED. Human corneal epithelial cells (HCECs) were exposed to hyperosmotic stress in vitro and treated with REB or DQS. Cell viability and cleaved caspase-3 expression were evaluated using the MTT assay and Western blotting. DED was induced in vivo in C57BL/6 mice using subcutaneous scopolamine injection. Thereafter, the mice were assigned to normal control (NC), dry eye (DE), DQS-treated (DQS), or REB-treated (REB) groups. Clinical evaluations, including measurement of tear film break-up time, corneal smoothness, and the lipid layer, were performed on days 7 and 14. In addition, CD4+ IFN-γ+ T cells, inflammatory cytokines, reactive oxygen species (ROS), lipid peroxidation markers, and corneal apoptosis were analyzed on day 14. Glycocalyx integrity and goblet cell density were also evaluated. The results indicate that REB improved HCEC survival and suppressed cleaved caspase-3 expression more effectively than DQS (p < 0.05). Both treatments improved clinical outcomes in the murine dry eye model; however, REB showed superior efficacy in reducing ROS levels, lipid peroxidation, and apoptosis, and in preserving corneal glycocalyx integrity and conjunctival goblet cell density. These findings highlight the therapeutic potential and protective effects of REB against oxidative stress-related damage and apoptosis in DED.

## Linked entities

- **Proteins:** Casp3 (caspase 3)
- **Chemicals:** rebamipide (PubChem CID 5042), diquafosol (PubChem CID 148197)
- **Species:** Homo sapiens (taxon 9606), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}
- **Diseases:** inflammatory (MESH:D007249), DE (MESH:D015352)
- **Chemicals:** Rebamipide (MESH:C052785), ROS (MESH:D017382), scopolamine (MESH:D012601), lipid (MESH:D008055), MTT (MESH:C070243), Diquafosol (MESH:C403315)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12291863/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12291863/full.md

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Source: https://tomesphere.com/paper/PMC12291863