There are different methods to measure the unstable molecule nitric oxide (
NO). We will describe a new sensitive method to measure NO by reconversion
of nitrate/nitrite to NO, which will be determined with an amperometric Cla
rk-type electrode. Nitrate and nitrite are the degradation products of NO.
First, nitrate is enzymatically converted to nitrite with the use of the ni
trate reductase. Second, nitrite is reduced to equimolar NO concentrations
by an acidic iodide solution. The detection limit of the electrode in an aq
ueous solution was 2 nmol/l NO (meaning the threshold was depending on the
volume added: 500 mul of a 0.2 mu mol/l nitrite solution added to a 10-ml b
ath). This method provides the ability to assess basal and agonist-stimulat
ed NO releases of different biological models. We measured basal and carbac
hol-stimulated NO release of native endothelial cells from porcine coronary
arteries and porcine aortic endothelial cell cultures. Moreover, it was po
ssible to measure the nitrate! nitrite concentration in the coronary efflue
nt of a guinea pig heart. In conclusion, we present a valid, highly sensiti
ve new method of measuring nitrite/NO in biological systems with a commerci
ally available electrode.