Abstract

BackgroundDry eye (DE) is a common eye disease, and appropriate animal models are essential to explore the pathogenesis and therapy of DE. In this study, we aimed to establish rabbit models by three methods.MethodsIn group A, the lacrimal gland, Harderian gland, and nictitating membrane of the left eyes were surgically removed. In group B, the bulbar conjunctiva of the left eyes was burned with 50% trichloroacetic acid. In group C, both methods above were used. The right eyes served as normal controls. The Schirmer I test (SIt), fluorescein staining, and impression cytology were evaluated at baseline and on days 28, 42, and 56.ResultsBoth the SIt and goblet cell density were significantly lower in operated eyes compared to the control eyes, while the corneal fluorescein staining scores in the operated eyes were significantly higher than in the control eyes on days 28, 42, and 56 (p < 0.05, p < 0.01 or p < 0.001). The SIt and goblet cell densities in groups B and C were significantly lower than group A on days 28, 42, and 56 (p < 0.05, p < 0.01 or p < 0.001). In addition, the corneal fluorescein staining scores in group C were significantly higher than either group A or group B on days 28, 42, and 56, while fluorescein staining scores were higher in group B than group A on days 42 and 56 days (p < 0.05, p < 0.01 or p < 0.001), with mean score 3.8 ± 1.30 (group A), 7.4 ± 1.14 (group B) and 10.8 ± 1.30 (group C) on day 56.ConclusionsResults suggest that three separate DE models, with mild, moderate, and severe manifestations of DE, could be stably established, in which conjunctival goblet cells took an important role.

Highlights

  • Dry eye (DE) is a common eye disease, and appropriate animal models are essential to explore the pathogenesis and therapy of DE

  • The purpose of our study was to establish the above two rabbit models of DE as well as a third rabbit model that involved burning the bulbar conjunctiva with 50% trichloroacetic acid only to compare the three different models

  • The Schirmer I test (SIt) in the left eyes of group C was significantly lower than group B on days 28, 42, and 56 (p < 0.05 or p < 0.001), but no significant difference between groups A and B were noted at any time point (p > 0.05)

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Summary

Introduction

Dry eye (DE) is a common eye disease, and appropriate animal models are essential to explore the pathogenesis and therapy of DE. Dry eye (DE), referred to as keratoconjunctivitis sicca (KCS), is a multifactorial disease of the tears and ocular surface that cause discomfort, visual disturbance, and tear film instability, which can potentially damage the ocular surface. The clinical symptoms of DE vary from minor discomfort to dryness, a sensation of having a foreign body, asthenopia, photophobia, and pain, among others such as difficulty opening eyes and eyesight reduction. Together, these symptoms severely influence the quality of life for each patient [3,4]. Several studies reported the impact of DE on vision related

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