The microsomes from dehydroepiandrosterone (DHEA)-supplemented animals
are good hydroxyl radical scavengers, as demonstrated through electro
n spin resonance and deoxyribose degradation. The ability of DHEA-supp
lemented microsomes to react with superoxide radical was also demonstr
ated through the inhibition of nitroblue tetrazolium reduction determi
ned by superoxide radicals produced in a hypoxanthine-xanthine oxidase
system. DHEA-enriched microsomes, obtained from acutely DHEA-treated
rats, become resistant to iron-dependent lipid peroxidation triggered
by H2O2/FeSO4 and ascorbate/FeSO4. The direct addition of DHEA to micr
osomes from untreated rats failed to prevent iron-dependent lipid pero
xidation, even if the microsomes were preincubated with DHEA for up to
15 min, indicating that in vivo transformation is required before ant
ioxidant action can be exerted. (C) 1998 John Wiley & Sons, Ltd.