SENSITIVE QUANTITATION OF NITRIC-OXIDE BY EPR SPECTROSCOPY

Citation
K. Tsuchiya et al., SENSITIVE QUANTITATION OF NITRIC-OXIDE BY EPR SPECTROSCOPY, Free radical biology & medicine, 21(5), 1996, pp. 733-737
Citations number
17
Categorie Soggetti
Biology
ISSN journal
08915849
Volume
21
Issue
5
Year of publication
1996
Pages
733 - 737
Database
ISI
SICI code
0891-5849(1996)21:5<733:SQONBE>2.0.ZU;2-H
Abstract
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.