Autofluorescence from reduced pyridine nucleotides (PN) and oxidized f
lavoproteins (Fp) was measured in order to detect the difference in re
dox states in rabbit corneal epithelium. The enucleated rabbit eye was
mounted in an eye bank eye container with McCarey-Kaufman medium, and
the autofluorescence was measured using ocular redox fluorometry as a
function of depth. The PN signal distributed evenly whereas the Fp si
gnal was greater in the posterior epithelial region than in the anteri
or region (p < 0.05). The PN/Fp ratio, a sensitive indicator of tissue
redox state, was less in the posterior region. After the application
of 1 mM of potassium cyanide in the medium, the ratio increased signif
icantly in each layer (p < 0.001), and the difference between anterior
and posterior region diminished. These results indicate that ocular r
edox fluorometry has the potential to resolve the redox states of the
various layers of the corneal epithelium. The posterior region of the
epithelium is more active in mitochondrial respiration than the anteri
or region.