L. Mazur, INDUCTION OF MICRONUCLEATED ERYTHROCYTES BY MEA, AET, WR-2721 AND X-RAYS, Mutation research. Section on environmental mutagenesis and related subjects, 334(3), 1995, pp. 317-322
The induction of micronucleated polychromatic erythrocytes (MNPCEs) wa
s assessed in the bone marrow of adult male Swiss mice treated with ME
A (cysteamine HCl), AET (2-aminoethylisothiouronium Br.HBr), or WR-272
1 (S-2-(3-aminopropylamino)ethyl phosphorothioic acid), at a dose of 2
00 mg/kg body weight, and/or exposed to 6 Gy X-rays. MEA, AET, or WR-2
721 was given alone or 15 min prior to X-ray exposure, and the frequen
cy of MNPCEs was determined 24 h after the aminothiol treatment and X-
irradiation of mice. A genotoxic effect was shown for MEA, AET, WR-272
1, and X-rays, as well as a protective effect of the aminothiols again
st X-ray-induced genotoxicity in the mouse erythropoietic system. The
aminothiol drugs given alone, without subsequent X-irradiation, elevat
ed the frequency of MNPCEs, and WR-2721 appeared to be less toxic than
AET and MEA. After exposure of mice to X-rays, the number of MNPCEs w
as distinctly increased. MEA, AET, or WR-2721 administration prior to
X-irradiation resulted in a reduction of the X-ray-induced elevation o
f the frequency of micronuclei, but a stronger radioprotective effect
was obtained following WR-2721 and AET treatment than after MEA applic
ation. So, the genotoxic and radioprotective effect of the aminothiols
was dependent on the compound applied.