Steel-Goodwin L, Kendrick J M, Egan J E, Eckstein J M
Department of Radiation Biophysics, Armed Forces Radiobiology Research Institute, Bethesda, MD 20889-5145.
Ann Clin Lab Sci. 1992 May-Jun;22(3):182-8.
Studies were made on the radioprotective and toxic effects of orally administered WR-151327 in male CD2F1 mice. The lowest dose of orally administered drug permitting probit analysis of data was 450 mg per kg. The calculated radioprotective dose reduction factors (DRF) at 450 mg per kg and 900 mg per kg of body weight (BW) WR-151327 were 1.2 and 1.3, respectfully. Pathological examination at 8, 30 or 90 days post administration of 100, 450, or 900 mg per kg of the drug demonstrated that the major target organ for orally dosed mice was the testes. There was a decrease in the number of cells in the germinal cell layers of testes from animals administered 450 mg per kg WR-151327 or 10 Gy whole body irradiation after eight days. Moreover, there was a dramatic reduction in the germinal cells in mice seminiferous tubules treated with a combination of 450 mg per kg WR-151327 plus 10 Gy radiation after eight days.
对雄性CD2F1小鼠口服WR-151327的辐射防护和毒性作用进行了研究。可对数据进行概率分析的口服药物最低剂量为每千克450毫克。每千克体重(BW)450毫克和900毫克WR-151327时计算出的辐射防护剂量降低因子(DRF)分别为1.2和1.3。给药后8、30或90天对每千克体重100、450或900毫克药物进行的病理检查表明,口服给药小鼠的主要靶器官是睾丸。给药每千克体重450毫克WR-151327的动物或八天后接受10 Gy全身照射的动物,其睾丸生精细胞层中的细胞数量减少。此外,八天后,每千克体重450毫克WR-151327加10 Gy辐射联合处理的小鼠生精小管中的生殖细胞显著减少。