Protection against endotoxemia in rats by a novel tetrahydrobiopterin analogue

We studied the effects of a novel pterin antagonist of NO synthase, the 4-amino analogue of tetrahydrobiopterin (4-ABH 4 ), in a rat model of endotoxic shock and compared its properties with those of N G -monomethyl L-arginine (L-NMMA). Treatment with a bolus dose of 4-ABH 4 at 2 h after LPS challenge significantly improved the 6-day survival rate, compared with the controls treated with saline. L-NMMA treatment did not significantly influence the survival rate. This bolus treatment, using either compound, had no effect on the plasma nitrite + nitrate or plasma IL-6 levels. The continuous infusion of 4-ABH 4 efficiently suppressed the enhanced calcium-dependent/independent NO synthase activities induced by endotoxin in lung homogenates and completely suppressed the increase in plasma nitrite + nitrate caused by endotoxin at 5 h with no significant difference compared with the L- NMMA treatment. Treatment of RAW264.7 murine macrophages with 4-ABH 4 but not with L-NMMA suppressed endotoxin-induced tumor necrosis factor-a release by the cells, whereas nitrite in the supematant decreased in a dose-dependent fashion in both assay systems. Our data show that 4-ABH 4 , an inhibitor of inducible NO synthase, significantly improves survival in a rat model of endotoxic shock when administered in a bolus dose that does not reduce plasma total nitrite + nitrate levels. Because we observed no overt signs of toxicity and no influence on organ-specific tetrahydrobiopterin levels, we conclude that the novel compound 4-ABH 4 is a promising drug candidate for protection against endotoxin-related mortality.