Transformations of 2,6-diisopropylphenol by NO-derived nitrogen oxides, particularly peroxynitrite

To investigate the protective effect of the anesthetic 2,6-diisopropylphenol, or propofol, in oxidative processes in which (NO)-N-. and peroxynitrite are involved, direct interactions were explored. The reactions of the highly lipophilic propofol with (NO)-N-. in methanolic or aqueous buffered solutions under air were shown to produce the same compounds as those detected with peroxynitrite, hut with very low yields and slow rates. In aqueous neutral medium, peroxynitrite (ONOO-, ONOOCO2-, ONOOH) was able to nitrate and oxidize propofol: In addition to oxidation products, quinone and quinone dimer, the formation of the 1-nitropropofol derivative was detected, increasing with peroxynitrite or CO2 concentrations. Nitration reached 20% after the addition of 25 mM bicarbonate to an equimolecular mixture of peroxynitrite and propofol in methanol/ phosphate-buffered solution (1/4,v/v) at pH 7.4. However, peroxynitrite either in methanol or in alkaline-buffered mixture (optimum pH 10-12) resulted in the rapid and almost complete transformation of propofol to an intermediate compound 1, which further decomposed to 4-nitrosopropofol. The transient compound 1 was obtained from either peroxynitrite or (NO)-N-. in the presence of oxygen. From mass spectrometry determination of compound 1 we propose the involvement of the nitrosodioxyl radical ONOO., forming an adduct with the propofoxyl radical, to yield 4-nitrosodioxypropofol and finally 4-nitrosopropofol. (C) 2000 Academic Press.