Effect of the Inducible Nitric Oxide Synthase Inhibitors Aminoguanidine and L-N6-(1-Iminoethyl)lysine on Zymosan-Induced Plasma Extravasation in Rat Skin

Abstract

The effect of nitric oxide synthase (NOS) inhibitors on plasma extravasation in a rat model of zymosan-induced inflammation has been investigated. Plasma extravasation was determined in response to intradermal test agents over 0 to 45 min or 0 to 4 h by the accumulation of i.v. injected 125I-labeled human serum albumin. Zymosan (1-100 μg/site) produced a dose- and time-dependent plasma extravasation. NG-nitro-L-arginine methyl ester (30-300 nmol/site), but not aminoguanidine (AG; 10-300 nmol/site) or L-N6-(1-iminoethyl)lysine (L-NIL; 10-300 nmol/site), significantly (p < 0.01) inhibited zymosan-induced (10 μg/site) plasma extravasation over 0 to 45 min. However, both AC and L-NIL produced significant (p < 0.05) inhibition over 0 to 4 h. The inhibition produced by AC was reversed by i.v. L-arginine or by coinjection of the vasodilator, calcitonin gene-related peptide. Zymosan (10-100 μg/site) induced an increase in dermal blood flow (laser-Doppler flowmetry) and this was inhibited by AC. Neutrophils were depleted selectively with antiserum, but this did not affect plasma extravasation except at the highest dose of zymosan (100 μg/site). Furthermore, zymosan-induced edema was not modified at either time point by pretreatment with the cyclooxygenase inhibitor indomethacin (30 μmol/kg, s.c., -30 min). In conclusion, in this model of dermal inflammation, it is suggested that inducible NOS inhibitors selectively remove an inducible NOS component that, at least in part, acts to increase microvascular blood flow and thus the edema formation observed during 0 to 4 h. There is no evidence of a contributory role for neutrophils or cyclooxygenase products in this model. Show more