A recent method for NO detection is electron paramagnetic resonance (E
PR) with ferrous and mononitrosyl dithiocarbamate (Fe2+ (DETC)(2)) for
spin trapping [Menon, N. K., et al., J. Mol. Cell Cardiol., 23:389; 1
991]. However, by this technique, we failed to detect the spectrum of
the NOFe2+(DETC)(2) complex in biological systems because of the low s
olubility of Fe2+(DETC)(2) and rapid oxidation of the NOFe2+(DETC)(2)
complex. To overcome these problems, we modified this method by adding
albumin to solubilize Fe2+ (DETC)2 and Na2S2O4 as a strong reductant
to increase the sensitivity and stability of the EPR spectrum of the N
OFe2+ (DETC)(2) complex. The optimal concentrations of these reagents
were 3.3 mM of Fe2+ and DETC, 33 mg/ml albumin and 2 M Na2S2O4. The de
tection limit was less than 10 pmol/ml under these conditions. By this
modified method, we succeeded in quantifying NO production from porci
ne aorta induced by forskolin.