ENDOGENOUS PEROXYNITRITE IS INVOLVED IN THE INHIBITION OF MITOCHONDRIAL RESPIRATION IN IMMUNO-STIMULATED J774.2 MACROPHAGES

The free radicals nitric oxide (NO) and surperoxide (O-2(-)) are known to react to form peroxynitrite (ONOO-), a potentially more injurious species. Here we compared the inhibitory effects of ONOO- and NO on mi tochondrial respiration in J774.2 macrophages. In addition, using uric acid, a potent scavenger of ONOO-, we investigated the potential invo lvement of endogenous ONOO- in the inhibitory effects of bacterial lip opolysaccharide (LPS) and gamma-interferon (IFN) on mitochondrial resp iration. The NO donors S-nitroso-N-acetyl-DL-penicillamine (SNAP, 1 mM ) or diethylamine NONOate (DN, 1 mM) inhibited cellular respiration by approximately 30% over 24h. Equimolar amounts of ONOO- caused a more pronounced inhibition of cell respiration. There was a synergistic eff ect between the O-2(-) generator pyrogallol (10 mu M-1 mM) and the NO donor SNAP (1 mM) in inhibiting mitochondrial respiration. The ONOO- s cavenger uric acid (UA, 1 mM) did not prevent the decrease in viabilit y in response to SNAP, DN or pyrogallol, but significantly prevented t he decrease in cell viability in response to ONOO-, to the combination of SNAP and pyrogallol, and to SIN-1, a compound that simultaneously generates NO and O-2(-). The decrease in mitochondrial respiration in response to LPS and IFN was also inhibited by UA as well as by N-G-met hyl-arginine, an inhibitor of NOS. Thus, ONOO is a more potent suppres sant of mitochondrial respiration than NO and endogenous formation of ONOO- appears to be involved in the cytotoxicity associated with immun e stimulation. (C) 1995 Academic Press, Inc.