Grdina D J, Garnes B A, Nagy B
Biological and Medical Research Division, Argonne National Laboratory, Argonne, Illinois 60439, USA.
Adv Space Res. 1992;12(2-3):257-63. doi: 10.1016/0273-1177(92)90115-e.
Two thiophosphoroate compounds WR-2721 and WR-151327 were assessed for their ability to modify the deleterious effects (life shortening and carcinogenesis) of fission-spectrum neutrons (kerma-weighted mean energy of 0.85 MeV) or gamma rays on B6CF1 hybrid mice. Male and female mice, 200 of each sex per experimental group, were irradiated individually at 110 days of age. Radioprotectors (400 mg/kg of WR-2721 or 580 mg/kg of WR-151327) were administered intraperitoneally 30 min prior to irradiation. Neutron doses were 10 cGy or 40 cGy and gamma ray doses were 206 cGy or 417 cGy. Animals were housed five to a cage; cage locations in the holding rooms were randomized by computer. Animals were checked daily and all deceased animals were necropsied. WR-2721 afforded protection against both neutron- and gamma-ray-induced carcinogenesis and subsequent life shortening. Cumulative survival curves for unirradiated mice of either sex were unaffectecd by protectors. WR-2721 protected irradiated groups against life shortening by approximately 10 cGy of neutrons or 100 cGy of gamma rays. WR-151327 was as effective as WR-2721 against neutron irradiation.
评估了两种硫代磷酸酯化合物WR-2721和WR-151327改变裂变谱中子(比释动能加权平均能量为0.85兆电子伏)或γ射线对B6CF1杂交小鼠的有害影响(寿命缩短和致癌作用)的能力。每个实验组有200只雄性和200只雌性小鼠,在110日龄时单独进行照射。在照射前30分钟腹腔注射辐射防护剂(400毫克/千克的WR-2721或580毫克/千克的WR-151327)。中子剂量为10厘戈瑞或40厘戈瑞,γ射线剂量为206厘戈瑞或417厘戈瑞。动物每笼饲养5只;饲养室中的笼子位置通过计算机随机安排。每天检查动物,对所有死亡动物进行尸检。WR-2721对中子和γ射线诱导的致癌作用以及随后的寿命缩短均有防护作用。保护剂对未受照射的任何性别的小鼠的累积生存曲线均无影响。WR-2721保护受照射组免受约10厘戈瑞中子或100厘戈瑞γ射线导致的寿命缩短。WR-151327在抗中子照射方面与WR-2721效果相同。