Increased iris vessel permeability observed in diabetics has also been repo
rted to occur in diabetic animals and galactose-fed rats. The potential rol
e of aldose reductase in the induction of iris vessel changes has been inve
stigated in rats fed a 50%, galactose diet with/without the aldose reductas
e inhibitors AL 1576, sorbinil or ponalrestat for 7 to 18 months. Compared
to normal control rats, long-term galactose-fed rats display a breakdown of
the blood-aqueous barrier due to iris vessel changes that include focal st
raightening, dilation, constriction, increased permeability, ischemia and n
ew vessel proliferation. The onset and progression of these iridal vessel c
hanges were prevented by the aldose reductase inhibitors AL 1576 and sorbin
il, and reduced by Ponalrestat, Computerized analyses of lumen areas of iri
s vessels indicated an 18-fold decrease in the vascular area near the pupil
lary boarder in untreated galactose-fed rats compared with age-matched cont
rols and galactose-fed rats treated with aldose reductase inhibitors, These
observations linking iris vessel changes with galactose-feeding, coupled w
ith the fact that aldose reductase inhibitors also prevent these changes, s
trongly suggest a link between the sorbitol pathway and the appearance and
progression of iris vessel changes. (C) 1999 Academic Press.