Nitric oxide (NO) has been detected in the exhaled gas of animals and human
s. In previous work, investigators have used anesthetized, mechanically ven
tilated animals to obtain exhaled NO (E-NO) measurements, which has unclear
effects on the levels of END and does not allow for repeated analysis of E
-NO. We sought to measure E-NO from a single, spontaneously breathing mouse
. The mouse was placed in a small Plexiglas chamber and allowed to acclimat
ize before exhaled gas was collected for E-NO analysis. Under optimal opera
ting conditions of flow and pressure, the mean concentration of exhaled NO
(FENO) Of 25 mice was 10.1 +/- 1.0 ppb. The maximal variation of FEND when
repeatedly measured daily in individual animals was 2.1 ppb. Administration
of L-NAME, a nonselective NOS inhibitor, reduced FENO by 51 +/- 6% (p < 0.
01). Intraperitoneally administered lipopolysaccharide induced acute lung i
njury and increased FENO by 30 +/- 7% (p < 0.05). We have demonstrated that
it is possible to noninvasively measure E-NO from a single, spontaneously
breathing mouse. This novel technique provides a stable, reproducible, and
responsive measure of E-NO in mice. This technique will be of use in determ
ining cellular and isoform sources of E-NO, as well as the role of endogeno
us NO in lung disease.