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Corneal Epithelial Abrasion with Ocular Burr As a Model for Cornea Wound Healing
Published on: July 10, 2018
Spontaneous corneal dystrophy and generalized basement membrane changes in Fischer-344 rats
R H Bruner1, W F Keller, K A Stitzel
1Pathology Associates, Inc., West Chester, Ohio 45069-3866.
Toxicologic Pathology
|January 1, 1992
Summary
Corneal basement membrane dystrophy is common in Fischer-344 rats. Advanced eye lesions correlated with more severe basement membrane changes in other organs, suggesting a common underlying cause.
Area of Science:
- Ophthalmology
- Pathology
- Toxicology
Background:
- Corneal basement membrane lesions, or corneal dystrophy, are a potential concern in research animals.
- Fischer-344 rats are a common model organism in toxicological studies.
Purpose of the Study:
- To determine the prevalence and severity of corneal basement membrane lesions in Fischer-344 rats.
- To investigate potential correlations between ocular and nonocular basement membrane changes.
- To assess the impact of these lesions on the suitability of rats as biologic test systems.
Main Methods:
- Ophthalmological and histopathological examinations were performed on young, sexually mature Fischer-344 rats (n=25/sex).
- Rats were sourced from multiple commercial breeders.
- Severity of corneal lesions and basement membrane changes in nonocular tissues (renal tubules, vascular internal laminae) were evaluated.
Main Results:
- A high incidence of corneal basement membrane dystrophy was observed across all breeders.
- Rats from one specific breeder exhibited significantly increased lesion severity.
- Advanced corneal lesions were associated with more severe basement membrane changes in renal tubules and vascular internal laminae.
Conclusions:
- Ocular and nonocular dystrophic changes in Fischer-344 rats may share common physiologic or genetic mechanisms.
- The presence of basement membrane lesions did not compromise the animals as biologic test systems.
- Breeder origin is a significant factor influencing the severity of corneal dystrophy in this rat model.

