Induction of inducible nitric oxide synthase (iNOS) following corneal infec
tion with herpes simplex virus type-1 (HSV-1) generates nitric oxide (NO),
an important player in the defense against viral infection. Changes in argi
nine metabolism during infection are not limited to effects of iNOS but can
also involve arginases, which can modulate NO synthesis and produce ornith
ine for the generation of polyamines and proline. The latter are important
molecules involved in tissue damage and repair during inflammation. In this
study we determined the responses of arginase I and II in a murine model o
f HSV-l-induced stromal keratitis (HSK). In the cornea iNOS and arginase II
mRNA were co-induced as the initial inflammation developed at 2 days posti
nfection (p.i.). As stromal keratitis progressed (days 8-15 p.i.) arginase
I mRNA was induced tenfold, in contrast to a moderate decrease in arginase
II and a loss of iNOS expression. These results suggest that elevated expre
ssion of arginase I and II in the cornea at late stages of ocular HSV-I inf
ection may play a role in lesion expression in HSK. (C) 2001 Elsevier Scien
ce B.V. All rights reserved.