The ultimate goal of in vivo electron spin resonance (ESR) spin trapping is
to provide a window to the characterization and quantification of free rad
icals with time within living organisms. However, the practical application
of in vivo ESR to systems involving reactive oxygen radicals has proven ch
allenging. Some of these limitations relate to instrument sensitivity and p
articularly to the relative stability of these radicals and their nitrone a
dducts, as well as toxicity limitations with dosing. Our aim here is to rev
iew the strengths and weaknesses of both traditional and in vivo ESR spin t
rapping and to describe new approaches that couple the strengths of spin tr
apping with methodologies that promise to overcome some of the problems, in
particular that of radical adduct decomposition. The new, complementary te
chniques include: (i) NMR spin trapping, which monitors new NMR Lines resul
ting from diamagnetic products of radical spin adduct degradation and reduc
tion, (ii) detection of (NO)-N-. by ESR with dithiocarbamate: Fe(II) "spin
trap-like" complexes, (iii) MRI spin trapping, which images the dithiocarba
mate: Fe(II)-NO complexes by proton relaxation contrast enhancement, and (i
v) the use of ESR to follow the reactions of sulfhydryl groups with dithiol
biradical spin labels to form "thiol spin label adducts," for monitoring i
ntracellular redox states of glutathione and other thiols. Although some of
these approaches are in their infancy, they show promise of adding to the
arsenal of techniques to measure and possibly "image" oxidative stress in l
iving organisms in real time. (C) 2001 Elsevier Science Inc.