The electronic structure of ground state oxygen, which is essential for the life of
all aerobic organisms, makes it potentially dangerous for those organisms.
Atmospheric oxygen contains two unpaired electrons with parallel spin states, which
predisposes it to reduction by a univalent pathway. As a consequence, normal aerobic
metabolism generates dangerous reactive intermediates of the reduction of
O
2
. These include superoxide radical
(O
2
–
), hydrogen peroxide
(H
2
O
2
), and hydroxyl radical (HO). These reactive
oxygen species and others that they can engender can damage all cellular
macromolecules and unless opposed by cellular defenses, would make aerobic life
impossible. Such defenses include superoxide dismutases, catalases, and peroxidases,
enzymes that decrease the concentration of the reactive oxygen species that are their
substrates, and others that repair or recycle oxidatively damaged macromolecules. Any
factor that stimulates reactive oxygen species production or suppresses the
antioxidant systems would inevitably cause cell damage. The role of such oxidative
damage in various diseases is well documented. In vivo detection of
O
2–
and other reactive oxygen species is however hampered by the
lack of easy, specific, and sensitive analytical methods. Potential artifacts and
limitations of the most common detection methods currently in use are briefly
discussed.