首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Induction of micronucleated erythrocytes by MEA, AET, WR-2721 and X-rays.
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Induction of micronucleated erythrocytes by MEA, AET, WR-2721 and X-rays.

机译:MEA,AET,WR-2721和X射线诱导微核红细胞。

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The induction of micronucleated polychromatic erythrocytes (MNPCEs) was assessed in the bone marrow of adult male Swiss mice treated with MEA (cysteamine HCl), AET (2-aminoethylisothiouronium Br.HBr), or WR-2721 (S-2-(3-aminopropylamino)ethyl phosphorothioic acid), at a dose of 200 mg/kg body weight, and/or exposed to 6 Gy X-rays. MEA, AET, or WR-2721 was given alone or 15 min prior to X-ray exposure, and the frequency of MNPCEs was determined 24 h after the aminothiol treatment and X-irradiation of mice. A genotoxic effect was shown for MEA, AET, WR-2721, and X-rays, as well as a protective effect of the aminothiols against X-ray-induced genotoxicity in the mouse erythropoietic system. The aminothiol drugs given alone, without subsequent X-irradiation, elevated 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 was distinctly increased. MEA, AET, or WR-2721 administration prior to X-irradiation resulted in a reductionof the X-ray-induced elevation of the frequency of micronuclei, but a stronger radioprotective effect was obtained following WR-2721 and AET treatment than after MEA application. So, the genotoxic and radioprotective effect of the aminothiols was dependent on the compound applied.
机译:在成年雄性瑞士小鼠的骨髓中用MEA(半胱胺HCl),AET(2-氨基乙基异硫脲Br.HBr)或WR-2721(S-2-(3-)处理后,评估了其微核多色红细胞(MNPCEs)的诱导。剂量为200 mg / kg体重和/或暴露于6 Gy X射线。单独使用MEA,AET或WR-2721,或在X射线暴露前15分钟给予,并在氨基硫醇治疗和X射线照射小鼠后24小时确定MNPCE的频率。已显示出对MEA,AET,WR-2721和X射线具有遗传毒性作用,以及氨基硫醇对小鼠促红细胞生成系统中X射线诱导的遗传毒性的保护作用。单独使用氨基硫醇药物,无需随后的X射线辐照,可提高MNPCE的频率,并且WR-2721的毒性比AET和MEA低。小鼠暴露于X射线后,MNPCE的数量明显增加。 X射线照射前施用MEA,AET或WR-2721导致X射线诱导的微核频率升高降低,但是WR-2721和AET处理后获得的放射防护作用比MEA施加后强。因此,氨基硫醇的遗传毒性和放射防护作用取决于所用化合物。

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