A chromosome aberration test on bone marrow cells of C57B1/6 mice show
ed that beta-carotene (BC) applied by oral administration as a E160a f
ood dye (30% oil suspension) at doses of 0.5, 5, and 50 mg/kg simultan
eously with cyclophosphamide (CPA) and dioxydine (DN) injected intrape
ritoneally for a period of 24 h did not modify their clastogenic effec
ts. If the animals were pretreated with perorally administrated beta-c
arotene dye at doses of 5 and 50 mg/kg (corresponding to 1.5 and 15 mg
/kg of BC) for 5 consecutive days, a statistically significant reducti
on in the clastogenic effect of the DN injected for 24 h but not the C
PA was observed. In another set of experiments, E160a and clastogens w
ere administered simultaneously for 5 consecutive days, and the animal
s were killed 6 h after the last treatment. In this case, BC at the do
se of 0.15-15 mg/kg statistically significantly reduced the clasgenici
ty of DN at all doses used, and of CPA at doses of 1.5 and 15 mg/kg.