We have examined the effect of a G-Rutin and luteolin on doxorubicin (
DOX) toxicity in mice. In the heart, the lipid peroxide level, increas
ed to 1.5 times of the normal level induced by DOX, decreased to the n
ormal level after treatment with cl G-Rutin or luteolin (i.p.). Glutat
hione peroxidase (GSHpx) activity, decreased to 73% of normal activity
after DOX treatment, was shown to recover by the combined flavonoids.
The lipid peroxide level in bone marrow cells increased to 5.9 times
of the normal level by DOX treatment, whereas this level in the extra
bone marrow cells did not change by treatment with DOX. The combinatio
n of a G-Rutin and luteolin with DOX significantly inhibited the DOX i
nduced-increment of the lipid peroxide level in bone marrow cells. Fla
vonoids have also reduced the effect of DOX toxicity by oral administr
ation. It is suggested that it is possible to reduce DOX toxicity by t
he intake of food including flavonoids. In NADPH-deqendent lipid perox
idation, a G-Rutin and luteolin showed concentration-dependent inhibit
ion. Therefore, we considered that the reduction effect of DOX toxicit
y by flavonoids was caused by antioxidative action and other effect of
the flavonoids. (C) 1997 Elsevier Science Ireland Ltd.