Provost G S, Mirsalis J C, Rogers B J, Short J M
Stratagene, La Jolla, CA 92037, USA.
Environ Mol Mutagen. 1996;28(4):342-7. doi: 10.1002/(SICI)1098-2280(1996)28:4<342::AID-EM7>3.0.CO;2-D.
The genotoxic response of benzene and tris(2,3-dibromopropyl)-phosphate (TDBP) have been evaluated in several tissues using the standardized lambda/lacI (Big Blue) transgenic mouse mutation assay. Separate groups of four to five male B6C3F1 transgenic lambda/lacI mice were given oral administrations of benzene or TDBP at varying concentrations. Tissues evaluated include lung, bone marrow, and spleen in benzene-treated animals, and liver, kidney, and stomach in TDBP-treated animals. Significant increases in lacI mutations were observed in the spleen and bone marrow of benzene treated mice, and the kidneys of TDBP-treated mice. Where applicable, mutagenesis patterns of tissue sensitivity were consistent with what has been observed previously in other assays. In addition, mutagenicity in tissues not traditionally evaluated for mutations correlated to sites of carcinogenicity for the chemicals tested.
已使用标准化的λ/lacI(大蓝)转基因小鼠突变试验,在多个组织中评估了苯和磷酸三(2,3-二溴丙基)酯(TDBP)的遗传毒性反应。将四至五只雄性B6C3F1转基因λ/lacI小鼠分为不同组,分别给予不同浓度的苯或TDBP口服。所评估的组织在苯处理的动物中包括肺、骨髓和脾脏,在TDBP处理的动物中包括肝脏、肾脏和胃。在苯处理小鼠的脾脏和骨髓以及TDBP处理小鼠的肾脏中,观察到lacI突变显著增加。在适用的情况下,组织敏感性的诱变模式与先前在其他试验中观察到的一致。此外,在传统上未评估突变的组织中的诱变性与所测试化学品的致癌部位相关。