Background: Nitric oxide (NO) plays an important role in renal hemodynamics
and function. Although production of NO in the glomeruli has been found to
be increased in animal models of glomerulonephritis, it remains unclear wh
ether its endogenous production is enhanced in patients with chronic glomer
ulonephritis (CCN). Subjects and methods: We measured NO output in exhaled
air as an indicator of its local production in the lungs and plasma and uri
nary nitrite plus nitrate (NO2-/NO3-) levels as indicators of its productio
n in the whole body in 21 patients with CGN in 31 healthy controls. Results
: The patients exhaled higher concentrations of NO (29.5 +/- 1.4 vs. 18.7 /- 1.0 parts per billion (ppb), mean +/- SEM, p < 0.0001) and exhaled NO ou
tput was also higher than in controls (166.6 +/- 6.8 vs. 95.5 +/- 5.6 nl/mi
n/m(2), p < 0.0001) Plasma NO2-/NO3- concentrations were also significantly
greater in the patients than in the controls (81.6 +/- 7.2 vs. 41.1 +/- 4.
3 mu mol/l, p < 0.001). In patients with CGN, exhaled NO output correlated
negatively with creatinine clearance (r = -0.62, p < 0.05). Oral administra
tion of prednisolone (60 mg/day) for two weeks did not significantly affect
the exhaled NO output in the patients (160 +/- 7 vs. 200 +/- 30 nl/min/m(2
), p = NS) despite a decrease in urinary protein excretion (12.0 +/- 2.9 vs
. 1.4 +/- 0.6 g/day, p < 0.01). Conclusion: These findings suggested that e
ndogenous NO production is increased in patients with CGN. Increased endoge
nous NO production may play some pathophysiological role in these patients.