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Biomedical subjects

J K Warren

Publications and source records attributed to J K Warren.

2 recordsLinked to original sources

Effects of phacoemulsification and extracapsular lens removal on corneal thickness and endothelial cell density in the dog.

Twenty-one dogs were used to study the effects of phacoemulsification and extracapsular lens removal on corneal endothelium and corneal thickness. Specular microscopy revealed preoperative cell morphology and cell densities similar to man. After surgery endothelial cell counts significantly decreased 22% (central) and 13% (periphery) with phacoemulsification and 34% (central) and 31% (periphery) with extracapsular lens removal. Corneal thickness increased with both procedures. Endothelial cell pathology included cellular enlargement, increased pleomorphism, and focal cellular degeneration. Phacoemulsification time did not correlate with the degree of cell loss. Dog corneal endothelium responds to surgical trauma in a manner similar to man and maintains a functional monolayer via cellular enlargement and migration. The dog, therefore, represents a good animal model for the study of corneal endothelial disease in man.

Animals

Decrease in canine corneal endothelial cell density and increase in corneal thickness as functions of age.

Fifty-nine normal dogs, ranging in age from 6 weeks to 132 months were examined with contact specular microscopy to determine the relationship of age to corneal endothelial cell density, morphology, and corneal thickness. Canine corneal endothelial cells appear quite similar to those of other species studied, including man. The hexagonally shaped canine endothelial cells tend to enlarge with age, with the population in young animals averaging around 2500 cells/mm2 and the number of cells in older dogs being frequently below 2100 cells/mm2. A significant increase in corneal thickness was observed with age. Healthy canine corneal endothelial cells appear to maintain a functional monolayer by enlargement and migration and represent a reasonable model for future endothelial cell study.

Age Factors