THE generation of nitrite (NO2-) was used as an index of the productio
n of nitric oxide by human and rat polymorphonuclear leukocytes (PMN)
and rat peritoneal macrophages. Human peripheral blood PMN did not pro
duce significant levels of NO2-. Attempts to induce NO2- generation in
human PMN by incubation with GM-CSF (1nM), TNF alpha (0.3 nM), endoto
xin (1 mu g/ml) or formyl-Met-Leu-Phe (100nM) for up to 16h were not s
uccessful. Addition of human PMN primed by GM-CSF (1nM) to rabbit aort
ic ring preparations precontracted with phenylephtine had no effect on
tone. In contrast to these observations, PMN, isolated from the perit
oneum of oyster glycogen treated rats, generated NO2 via a pathway sen
sitive to inhibition by the nitric oxide synthase inhibitor, N-G-monom
ethyl L-arginine. However, peripheral blood rat PMN obtained from the
same animals did not produce NO2-, even during prolonged incubation fo
r periods of up to 16 h. It is suggested that detectable NO production
by PMN requires NO synthase activity to be induced either by the proc
ess of PMN migration or by exposure to certain cytokines produced loca
lly at the site of inflammation.